Available Positions Head Office
Laboratory
Phase I Clinic
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why choose pharma medica research Inc?
Why Choose Pharma Medica Research Inc?
Pharma Medica Research Inc is a fast growing full service Contract Research Organization with locations in
Toronto, Ontario and in Mississauga, Ontario. Our clients are world-wide pharmaceutical and biotechnology companies, for whom we provide testing of new drug products. Our goal is to bring our clients’ products safely to market on time.
Our reputation for delivering high quality research is outstanding. Credit for this goes to our employees who take pride and satisfaction in maintaining our motto of “Quality on Time”.
We invite you explore the opportunities in our Current Job Postings and to discover why we believe Pharma Medica Research Inc is the best contract research organization in Canada today!
Our Growth
Since 1999, Pharma Medica Research has added over 240 positions. This number is constantly increasing, as we continue to expand. Pharma Medica continues to grow locally as our market expands across the world. Come grow with us.
Compensation & Benefits
Our compensation and benefits program is designed to attract, retain and motivate high achieving individuals with a dedication to excellence. Whether full-time, part-time or contract position, Pharma Medica offers competitive wage packages. Non-management and non-professional positions are also eligible for paid overtime. Pharma Medica is also proud to offer its full-time employees one of the most comprehensive benefits packages in our industry.
Benefits for full-time employees includes:
- 3 weeks paid vacation per year to start
- Paid sick leave program
Group health benefits for the employee and their family include:
- Dental coverage (basic dental, major dental and orthodontics)
- Dependent life insurance
- Accidental death and dismemberment
- Long term disability
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- Paramedical services coverage
- Vision care coverage
- Global medical assistance
- Out-of-country emergency care
- Critical illness insurance
- Extended health care
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All benefit premiums are fully paid for by Pharma Medica with the exception of Long Term Disability (for tax purposes)
Diversity
Pharma Medica is proud of the diversity of our workforce. Our employees come from a wide variety of backgrounds, cultures, and experiences. We are strengthened by the diversity of perspectives that our employees bring to our team. We value and are committed to an equitable workplace, where everyone can realize their full potential with equal access to opportunities.
Health & Safety
Pharma Medica is committed to providing a safe workplace for all employees, visitors, subjects and to the global community. Health and safety at Pharma Medica is an integral part of business performance. Pharma Medica is committed to providing adequate resources to implement the health and safety policies and practices. The management of health and safety is a prime responsibility of management, from the most senior executive to the first line supervisory level. At Pharma Medica, we understand that we must all work together to create a safe environment for all of us.
How To Apply
If you would like to join our team of qualified and exceptional employees, please submit your resume in confidence in one of the following ways:
| BY E-MAIL |
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BY MAIL |
jobs@pharmamedica.com |
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Pharma Medica Research Inc
C/O Human Resources
6100 Belgrave Road
Mississauga, ON L5R 0B7 |
Please be sure to indicate which position you are applying for. While Pharma Medica thanks all applicants, only those selected for interview will be contacted. Pharma Medica is proud of its workforce diversity and welcomes all applications |
| Accounting (Assistant) |
| 75 Hours Bi-Weekly (Full Time) @ Head Office (Mississauga) |
| Updated: Wednesday, May 21, 2008 @ 5:47:00 PM |
| Job Summary |
| Responsible for accounts receivable (A/R) and assists accounts payable (A/P) and purchasing |
| Duties |
- Responsible for maintaining, recording and correlating supply requisition and packing slips with invoices
- Assist Human Resources department in recording and correlating manually written timesheets with Master Sheet and input into Accpac
- Following up on any discrepancies in invoices
- Responsible for full accounts receivable functions including issuing customer invoices, applying payments and following up on overdue accounts
- Responsible for monthly report to controller and various department heads
- Responsible for setting up projects in job costing module in a timely manner
- Assist in issuing supplier purchase orders
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| Qualifications |
- Enrolled in formal accounting program such as the CGA
- 2-4 years experience in accounts receivable/payable or accounting position
- Strong computer skills required, experience with Accpac preferred
- Excellent interpersonal, written and oral skills
- Ability to work effectively in a team environment
|
Apply in confidence to: jobs@pharmamedica.com
with Job #24801 indicated in the subject line
Applicants are thanked in advance for their interest however only
those candidates selected for an interview will be contacted.
All qualified candidates are encouraged to apply.
Pharma Medica is committed to a diversified workplace.
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| Application Developer |
| 75 Hours Bi-Weekly (Full Time) @ Head Office (Mississauga) |
| Updated: Wednesday, February 11, 2009 @ 2:24:00 PM |
| Job Summary |
| The Application Developer will develop in .NET and develop, deploy and support n-Tier business applications built on .NET |
| Duties |
- Write Use Cases and other design documents for new application development
- Experience developing in .NET (ASP.NET and C# or VB, Preference VB)
- Developed, deployed and supported n-Tier business applications built
- Work closely with the technical staff, QA and customer to ensure that developed functionality meets requirements
- Experience using an object-oriented methodology and object-oriented analysis and design (OOAD)
- Ability to translate business requirements into high-level and detailed functional specifications
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| Qualifications |
- Microsoft Certified Professional (.NET, C#, ASP.NET, IIS, SQL Server or other .NET-centric certifications for Microsoft or other certification providers)
- Excellent English communication skills and ability to work effectively in a team environment
- At least 2 years experience with UML and writing Use Cases
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Apply in confidence to: jobs@pharmamedica.com
with Job #23903 indicated in the subject line
Applicants are thanked in advance for their interest however only
those candidates selected for an interview will be contacted.
All qualified candidates are encouraged to apply.
Pharma Medica is committed to a diversified workplace.
|
| Ass Project Manager |
| 75 Hours Bi-Weekly (Full Time) @ Head Office (Mississauga) |
| Updated: Monday, March 29, 2010 @ 11:55:00 AM |
| Job Summary |
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| Duties |
- Validate new and existing computerized systems for compliance with company SOPs, CSV program, and related regulatory requirements
- Create and maintain all corresponding validation documentation (i.e. master validation plan, CSV assessments, validation plan, IQ, OQ, PQ, CSV reports)
- Evaluate and maintain change controls
- Establish revalidation intervals and perform revalidation procedures
- Implement and maintain compliance with FDA 21 CFR Part 11
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| Qualifications |
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Apply in confidence to: jobs@pharmamedica.com
with Job #15103 indicated in the subject line
Applicants are thanked in advance for their interest however only
those candidates selected for an interview will be contacted.
All qualified candidates are encouraged to apply.
Pharma Medica is committed to a diversified workplace.
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| Assistant Project Manager |
| 75 Hours Bi-Weekly (Full Time) @ Head Office (Mississauga) |
| Updated: Monday, March 29, 2010 @ 11:53:00 AM |
| Job Summary |
| Determine sponsors requirements and effectively communicate information with PMRI to conduct clinical studies |
| Duties |
- Interact with clients to determine needs and effectively communicate this information with PMRI personnel
- Ensure the master schedule is accurate and up-to-date for Phase I trials taking into consideration limited departmental resources and timelines
- Manage progress of all ongoing projects assigned
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| Qualifications |
- Bachelors of Science
- 1-2 years experience in pharma/CRO or customer service
- Strong organization skills and attention to detail
- Ability to multi-task and ready to learn within PMRI
- Excellent interpersonal skills and ability to communication with team members and clients
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Apply in confidence to: jobs@pharmamedica.com
with Job #15101 indicated in the subject line
Applicants are thanked in advance for their interest however only
those candidates selected for an interview will be contacted.
All qualified candidates are encouraged to apply.
Pharma Medica is committed to a diversified workplace.
|
| Biostatistician |
| 75 Hours Bi-Weekly (Full Time) @ Head Office (Mississauga) |
| Updated: Tuesday, January 13, 2009 @ 12:06:00 PM |
| Job Summary |
| Perform data analyses, study design and interpretation of clinical trial results |
| Duties |
- Perform data analyses using SAS® for Phase I-IV clinical studies
- Perform data analysis on Phase-I Pharmacokinetic (PK), and comparative bioavailability (BA) studies
- Generate listings, tabulations, graphical presentations and summary statistics to support regulatory submissions
- Participate in the development of study designs including power and sample size calculations
- Prepare statistical analysis plans and randomization schemes for clinical trials
- Participate in the design, creation and validation of databases for clinical trials data
- Provide statistical advice and/or solutions to sponsors
- Assist in creating, maintaining, optimizing and validating existing SAS® programs
- Develop, write, implement and maintain standard operating procedures related to the Scientific Affairs department
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| Qualifications |
- M.Sc. in Mathematics and/or Statistics
- 2 to 3 year of experience in statistical analyses preferably biostatistical analysis
- Excellent computer skills and SAS® programming
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Apply in confidence to: jobs@pharmamedica.com
with Job #16803 indicated in the subject line
Applicants are thanked in advance for their interest however only
those candidates selected for an interview will be contacted.
All qualified candidates are encouraged to apply.
Pharma Medica is committed to a diversified workplace.
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| Computer System Validation Associate |
| 75 Hours Bi-Weekly (Full Time) @ Head Office (Mississauga) |
| Updated: Wednesday, May 12, 2010 @ 1:55:00 PM |
| Job Summary |
| Responsible for the PMRI CSV as well as FDA 21 CFR Part 11 initiatives |
| Duties |
- Validate new and existing computerized systems for compliance with company SOPs, CSV program, and related regulatory requirements
- Create and maintain all corresponding validation documentation (i.e. master validation plan, CSV assessments, validation plan, IQ, OQ, PQ, CSV reports)
- Evaluate and maintain change controls
- Establish revalidation intervals and perform revalidation procedures
- Implement and maintain compliance with FDA 21 CFR Part 11
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| Qualifications |
- Post secondary education in a related discipline
- 2-3 years experience in a CSV role, with sound knowledge of regulatory (FDA, Health Canada, EU) validation requirements/procedures
- Working experience with FDA 21 CFR Part 11
- Excellent interpersonal and organizational skills
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Apply in confidence to: jobs@pharmamedica.com
with Job #13806 indicated in the subject line
Applicants are thanked in advance for their interest however only
those candidates selected for an interview will be contacted.
All qualified candidates are encouraged to apply.
Pharma Medica is committed to a diversified workplace.
|
| Pharmacokineticist |
| 75 Hours Bi-Weekly (Full Time) @ Head Office (Mississauga) |
| Updated: Friday, May 23, 2008 @ 11:28:00 AM |
| Job Summary |
| Perform data analyses, study design and review of clinical trial reports |
| Duties |
- Perform pharmacokinetic analysis for Phase I-IV clinical trials
- Perform pharmacokinetic and statistical analysis for comparative bioavailability trials
- Execute pharmacokinetic and/or pharmacodynamic modeling as required
- Prepare well researched study designs
- Review protocol and study reports for scientific content, data accuracy and compliance with current regulatory guidelines
- Responsible for acquiring and maintaining knowledge of national and international guidelines
- Develop, write, implement and maintain standard operating procedures related to the Scientific Affairs department
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| Qualifications |
- M.Sc. in pharmacokinetics
- Experience in design and conduct of bioavailability and bioequivalence studies
- User-level knowledge of pharmacokinetic and statistical software
- Excellent English communication skills
- Ability to work effectively in a team environment
|
Apply in confidence to: jobs@pharmamedica.com
with Job #16802 indicated in the subject line
Applicants are thanked in advance for their interest however only
those candidates selected for an interview will be contacted.
All qualified candidates are encouraged to apply.
Pharma Medica is committed to a diversified workplace.
|
| Protocol Writer |
| 75 Hours Bi-Weekly (Full Time) @ Head Office (Mississauga) |
| Updated: Tuesday, November 04, 2008 @ 11:44:00 AM |
| Job Summary |
| Responsible for all actions relating to protocol development and maintenance |
| Duties |
- Generate protocols, informed consent forms, amendments and protocol summary documents
- Prepare documentation and reports related to the inclusion and/or exclusion requirements of the study
- Properly complete documentation in accordance with GCP, SOP guidelines, and/or FDA/TPD regulations for clinical trials (primarily Phase I studies)
- Enter ERB approved study related information into a computer management system
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| Qualifications |
- Bachelor of Science in a related field
- Post-graduate training in the pharmaceutical field is an asset
- Advanced English written and verbal skills
- Proficient in Microsoft Office and ADOBE software
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Apply in confidence to: jobs@pharmamedica.com
with Job #16805 indicated in the subject line
Applicants are thanked in advance for their interest however only
those candidates selected for an interview will be contacted.
All qualified candidates are encouraged to apply.
Pharma Medica is committed to a diversified workplace.
|
| QC Reviewer |
| 75 Hours Bi-Weekly (Full Time) @ Head Office (Mississauga) |
| Updated: Tuesday, November 03, 2009 @ 8:08:00 AM |
| Job Summary |
| Review raw analytical data and generate reports with accuracy and compliance as per study protocols. |
| Duties |
- Ensure that all reports and accompanying raw data are accurate, correct and acceptable according to the study protocol and relevant SOPs
- Production of data tables and reports in accordance with protocols and input from Principal Bioanalytical Investigator/Laboratory Technicians using Microsoft Word and Excel
- Follow-up on corrective action and/or answer and follow-up questions indicated on QA raw data and report audits, as well as, performing corrective action or answer inquiries indicated in sponsor review of data and/or reports
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| Qualifications |
- B.Sc. or College Diploma in related field
- Knowledgeable in the interpretation of analytical data and statistical analyses
- min 1 year analytical/research lab experience, CRO experience is preferred
- Proficient in Microsoft Office
- Ability to communicate clearly and effectively with other employees
|
Apply in confidence to: jobs@pharmamedica.com
with Job #23803 indicated in the subject line
Applicants are thanked in advance for their interest however only
those candidates selected for an interview will be contacted.
All qualified candidates are encouraged to apply.
Pharma Medica is committed to a diversified workplace.
|
| Quality Assurance Associate |
| 75 Hours Bi-Weekly (Full Time) @ Head Office (Mississauga) |
| Updated: Tuesday, August 10, 2010 @ 2:48:00 PM |
| Job Summary |
| To perform audits on all aspects of clinical, analytical and statistical study reports |
| Duties |
- Perform audits of the following laboratory phases for compliance with Good Laboratory Practice (GLP) Regulations and Guidelines (i.e. FDA 21 CFR Part 58, OECD), associated Regulatory Guidelines, and Corporate Standard Operating Procedures including:
- Bioanalytical study data and reports,
- Bioanalytical method validation data and reports,
- On-study laboratory processes (sample receipt, standard preparation, extraction, analysis),
- Organic synthesis data and reports
- Perform audits of clinical study reports for compliance with GCP Regulations and Guidelines associated Regulatory Guidelines, and corporate Standard Operating Procedures
- Document findings and recommendations in audit reports
- Effectively monitor and follow-up on corrective actions
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| Qualifications |
- University degree in a Scientific Discipline (preferably Chemistry)
- 2-3 years Quality Assurance experience auditing bioanalytical laboratory data and clinical studies
- Excellent working knowledge of GLP and GCP
- Extremely meticulous with the desire to strive for excellence
- Exceptional organizational and interpersonal skills
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Apply in confidence to: jobs@pharmamedica.com
with Job #16804 indicated in the subject line
Applicants are thanked in advance for their interest however only
those candidates selected for an interview will be contacted.
All qualified candidates are encouraged to apply.
Pharma Medica is committed to a diversified workplace.
|
| Report Writer I |
| 75 Hours Bi-Weekly (Full Time) @ Head Office (Mississauga) |
| Updated: Wednesday, August 25, 2010 @ 1:56:00 PM |
| Job Summary |
| Generate reports for clinical trials according to current regulatory and sponsor requirements |
| Duties |
- Responsible for all aspects of clinical, analytical and statistical study reports
- Work with the necessary clinical, statistical, analytical, regulatory and quality assurance personnel in order to provide PMRI sponsors with accurate and timely report information
- Compile clinical documentation and perform data entry
- Prepare electronic files as required by regulatory agencies
- Prepare study documentation for archiving
- Responsible for acquiring and maintaining knowledge of national and international guidelines
- Develop, write, implement and maintain standard operating procedures related to the Report Writing department
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| Qualifications |
- B.Sc. in Life Sciences or related field
- 1-2 years report writing experience in the pharmaceutical industry is an asset
- Strong computer skills required
- Excellent interpersonal, written and oral skills
- Ability to work effectively in a team environment
|
Apply in confidence to: jobs@pharmamedica.com
with Job #16801 indicated in the subject line
Applicants are thanked in advance for their interest however only
those candidates selected for an interview will be contacted.
All qualified candidates are encouraged to apply.
Pharma Medica is committed to a diversified workplace.
|
| Senior Project Manager |
| 75 Hours Bi-Weekly (Full Time) @ Head Office (Mississauga) |
| Updated: Wednesday, September 01, 2010 @ 10:15:00 AM |
| Job Summary |
| Determine sponsors requirements and effectively communicate information with PMRI to conduct clinical studies |
| Duties |
- Interact with assigned clients to determine current and upcoming needs and effectively communicate this information with PMRI personnel.
- Manage progress of all ongoing projects assigned within PMRI in cooperation with key staff.
- Assure the timely delivery of project progress reports and results to PMRI clients.
- Prepare study quotations and budget proposals.
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| Qualifications |
- Bachelors Degree (science or business)
- 2 years experience in pharmaceutical/CRO/CMO industry
- Strong organizational skills and attention to detail
- Ability to multi-task and ready to grow and learn within PMRI
- Proven record of creative problem solving
- Excellent interpersonal skills and ability to communication with team members and clients
|
Apply in confidence to: jobs@pharmamedica.com
with Job #15802 indicated in the subject line
Applicants are thanked in advance for their interest however only
those candidates selected for an interview will be contacted.
All qualified candidates are encouraged to apply.
Pharma Medica is committed to a diversified workplace.
|
| Analytical Chemist (Organic Synthesis Lab) |
| 75 Hours Bi-Weekly (Full Time) @ Laboratory (Mississauga) |
| Updated: Wednesday, February 17, 2010 @ 2:01:00 PM |
| Job Summary |
| Performs multi-step organic chemical synthesis as per requirements for clinical trials studies. |
| Duties |
- Carrying out all chemistry projects within timeline and regulatory guidelines
- Responsible for reporting all work relevant results on time
- Reviewing and interpreting analytical data and final results
- Responsible for writing and reviewing project reports
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| Qualifications |
- University Degree in Chemistry with a strong understanding of analytical and organic chemistry (Masters preferred)
- Strong background in performing multi-step organic synthesis, carbohydrate chemistry, and peptides chemistry.
- Synthesis of complex organic molecules, novel drugs, and drug analogues (or its derivatives) and metabolites based on structures
- Experience in the synthesis of labeled organic compounds is asset
- Planning of chemistry projects, report writing, collection and interpretation of technical data (UV/Vis, IR, 1H 13C NMR, 2D NMR, LC-MS)
- Good interpersonal and communications skills
- Capable to work in a team working environment
|
Apply in confidence to: jobs@pharmamedica.com
with Job #23906 indicated in the subject line
Applicants are thanked in advance for their interest however only
those candidates selected for an interview will be contacted.
All qualified candidates are encouraged to apply.
Pharma Medica is committed to a diversified workplace.
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| Bioanalytical Analyst (Contract) |
| 75 Hours Bi-Weekly (Full Time) @ Laboratory (Mississauga) |
| Updated: Friday, January 08, 2010 @ 4:20:00 PM |
| Job Summary |
| To perform bioanalytical drug testing and analysis as per PMRI protocols |
| Duties |
- Assist in development and validation of bioanalytical methods
- Analyses of drugs in biological specimens for bioequivalence, bioavailability, ADME (absorption, distribution, metabolism and elimination) studies etc.
- Operates and maintains all principle laboratory equipment including but not limited to HPLC, LC/MS, and LC-MS/MS
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| Qualifications |
- B.Sc. or Community College diploma in Science, Chemical Technology or related science
- Minimum 2 years CRO/Lab experience
- Ability to work both independently and as a team member
|
Apply in confidence to: jobs@pharmamedica.com
with Job #23901 indicated in the subject line
Applicants are thanked in advance for their interest however only
those candidates selected for an interview will be contacted.
All qualified candidates are encouraged to apply.
Pharma Medica is committed to a diversified workplace.
|
| Bioanalytical Technician (Contract) |
| 75 Hours Bi-Weekly (Full Time) @ Laboratory (Mississauga) |
| Updated: Thursday, October 29, 2009 @ 2:29:00 PM |
| Job Summary |
| Carries out biological specimen processing primarily in support of bioanalytical drug testing and analysis |
| Duties |
- Processing biological samples for analyses of drugs for bioequivalence, bioavailability, ADME studies etc.
- Understands operations of all principle laboratory equipment including but not limited to HPLC, LC/MS, LC-MS/MS, balances, pH meters, pipettes, freezers, water system, equipment for sample extraction and evaporation and fume hoods
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| Qualifications |
- B.Sc. in Chemistry or related science field
- Ability to work both independently and as a team member with excellent communications skills in English
|
Apply in confidence to: jobs@pharmamedica.com
with Job #23801 indicated in the subject line
Applicants are thanked in advance for their interest however only
those candidates selected for an interview will be contacted.
All qualified candidates are encouraged to apply.
Pharma Medica is committed to a diversified workplace.
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| Organic Synthetic Chemist (Contract) |
| 75 Hours Bi-Weekly (Full Time) @ Laboratory (Mississauga) |
| Updated: Friday, July 16, 2010 @ 2:10:00 PM |
| Job Summary |
| Performs complex organic/enzymatic synthetic method development, method revision and organic analysis tasks, in conformance with Pharma Medica Research Inc.(PMRI) laboratory practices |
| Duties |
- Perform independently new complex organic/enzymatic synthetic tasks, of drug metabolites, impurities and other active compounds as assigned
- Able to perform a variety of highly sensitive operations.
- Extensive sustained dexterity is required to handle and dispose of safely, air sensitive, hazardous and highly toxic reagents required in the synthesis of complex organic compounds
- Synthesis of complex organic molecules, novel drugs, and drug analogues (or its derivatives) and metabolites based on structures
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| Qualifications |
- MSc/PhD with relevant hands-on experience in a organic synthesis
- Strong background in performing multi-step organic synthesis, carbohydrate chemistry, and peptides chemistry.
- Synthesis of complex organic molecules, novel drugs, and drug analogues (or its derivatives) and metabolites based on structures
- Good problem solving skills and shows innovation in ongoing process, to improve existing methods and procedures, productivity, and to patent new processed and compounds
- Experience in the synthesis of labeled organic compounds is asset
|
Apply in confidence to: jobs@pharmamedica.com
with Job #23806 indicated in the subject line
Applicants are thanked in advance for their interest however only
those candidates selected for an interview will be contacted.
All qualified candidates are encouraged to apply.
Pharma Medica is committed to a diversified workplace.
|
| Project Manager (Bioanalytical Lab) |
| 75 Hours Bi-Weekly (Full Time) @ Laboratory (Mississauga) |
| Updated: Friday, January 08, 2010 @ 4:29:00 PM |
| Job Summary |
| Responsible for managing assigned bioanalytical projects including nonclinical and clinical studies, bioanalytical method development, method validation and study sample analysis |
| Duties |
- Responsible for tracking all assigned ongoing bioanalytical method development, method validation, nonclinical and clinical trial sample analysis.
- Ensures that all laboratory personnel involved in the assigned project are trained on the analytical method
- Must understand, and ensure that the laboratory staff, under his/her supervision, operates according to regulatory agency guidelines, GLP procedures, Laboratory SOPs and Study Protocols
- Verify all raw data generated from bioanalytical studies, and communicate any problems or deviations to the Principal Bioanalytical Investigator/designate
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| Qualifications |
- B.Sc. or a Community College Diploma in science or related field
- 3-5 years of Bioanalytical or analytical laboratory experience
- Excellent knowledge of equipment, instrumentation, troubleshooting, GLP, HPFB and FDA guidelines
- Leadership qualities, in developing a team of individuals capable of producing a high quality throughput of bioanalytical measurements
|
Apply in confidence to: jobs@pharmamedica.com
with Job #23905 indicated in the subject line
Applicants are thanked in advance for their interest however only
those candidates selected for an interview will be contacted.
All qualified candidates are encouraged to apply.
Pharma Medica is committed to a diversified workplace.
|
| Clinic Assistant (Contract) |
| Approx 60 Hours Bi-Weekly (Part Time) @ Phase I Clinic (Toronto) |
| Updated: Thursday, September 03, 2009 @ 12:43:00 PM |
| Job Summary |
| To prepare the supplies and facility for healthy adult clinical trials and maintain during study. Shifts between 6am-10pm 7 days a week. |
| Duties |
- Perform general clinical duties to prepare for the clinical study (i.e. tube labelling, bunk-bed room preparation)
- Follow Joint Health and Safety rules and regulations at all times
- Performing clinical activities including serving meals, monitoring water restrictions, directing/guiding subjects
- Perform tasks required by the Supervisor (Clinic Assistant), MLA Group Leader/Study Coordinator deemed necessary to conduct a clinical study
|
| Qualifications |
- Personal Support Worker College Diploma or equivalent education and/or formalized training
- Ability to handle multiple work assignments
- English communication skills and ability to work effectively in a team environment
|
Apply in confidence to: jobs@pharmamedica.com
with Job #20802 indicated in the subject line
Applicants are thanked in advance for their interest however only
those candidates selected for an interview will be contacted.
All qualified candidates are encouraged to apply.
Pharma Medica is committed to a diversified workplace.
|
| Facility Cleaner |
| Approx 60 Hours Bi-Weekly (Part Time) @ Phase I Clinic (Toronto) |
| Updated: Thursday, September 10, 2009 @ 2:04:00 PM |
| Job Summary |
| Responsible for performing cleaning duties to ensure the facility is clean and maintained. Shift work required including 6am-2pm and 2pm-10pm Saturday/Sundays |
| Duties |
- All cleaning duties including staff and subject washrooms, eating areas, sleeping/bunkbed areas, dinning room and offices
- Follow Joint Health and Safety rules and ensure regulations are adhered to at all times
|
| Qualifications |
- OSSD/High School or equivalent
- Experience in facility cleaning
- English communication skills and ability to work effectively in a team environment
|
Apply in confidence to: jobs@pharmamedica.com
with Job #20803 indicated in the subject line
Applicants are thanked in advance for their interest however only
those candidates selected for an interview will be contacted.
All qualified candidates are encouraged to apply.
Pharma Medica is committed to a diversified workplace.
|
| Facility Cleaner (Night Shift) (Contract) |
| Approx 60 Hours Bi-Weekly (Part Time) @ Phase I Clinic (Toronto) |
| Updated: Thursday, September 03, 2009 @ 8:22:00 AM |
| Job Summary |
| Responsible for performing cleaning duties to ensure the facility is clean and maintained. Night shift 10pm - 6am |
| Duties |
- All cleaning duties including washrooms, sleeping areas, dinning room and offices
- Maintenance of the cleaning supply room
- Snow plowing with company truck based on need
- Must have a valid drivers license and a clean abstract
|
| Qualifications |
- OSSD/High School or equivalent
- Experience in facility cleaning and general repairs/maintenance
- English communication skills and ability to work effectively in a team environment
|
Apply in confidence to: jobs@pharmamedica.com
with Job #20910 indicated in the subject line
Applicants are thanked in advance for their interest however only
those candidates selected for an interview will be contacted.
All qualified candidates are encouraged to apply.
Pharma Medica is committed to a diversified workplace.
|
| Group Leader, MLA |
| 75 Hours Bi-Weekly (Full Time) @ Phase I Clinic (Toronto) |
| Updated: Monday, September 28, 2009 @ 8:24:00 AM |
| Job Summary |
| Ensure Phase I Clinical Trials are conducted as per PMRI and Regulatory Standards |
| Duties |
- Supervise and/or perform all aspects of the study procedures and ensure proper documentation of clinical activities in compliance with SOP, GCP guidelines, FDA/TPP regulations
- Assist with responses to QA/QC findings and subject follow-up
- Ensure general clinical duties are performed to prepare for the clinical study (i.e. tube labeling, bunk room preparation, set up bleeding stations, etc)
- Responsible for direct reports including MLA during shift and training records
- Completion of all assigned tasks to ensure completion of trial
- Ensuring MLA and other technical staff perform duties as prescribed in SOP/GCP
-
|
| Qualifications |
- Bachelors of Science or related Bachelors degree
- Medical Laboratory Technician program with OSMT and CPR certification is an asset but not required
- 2 years experience clinic research or relevant related experience
-
|
Apply in confidence to: jobs@pharmamedica.com
with Job #25801 indicated in the subject line
Applicants are thanked in advance for their interest however only
those candidates selected for an interview will be contacted.
All qualified candidates are encouraged to apply.
Pharma Medica is committed to a diversified workplace.
|
| HR Manager (Clinic) |
| 75 Hours Bi-Weekly (Full Time) @ Phase I Clinic (Toronto) |
| Updated: Thursday, July 23, 2009 @ 10:28:00 AM |
| Job Summary |
| Responsible for administration and management of human resources at PMRI Phase I Clinical Trials facility |
| Duties |
- Manage the human resources function at the Toronto Clinic location in accordance with current labour practices of Ontario and Canada
- Work with clinic management to manage employee productivity, including monitoring staff attendance, punctuality, and any violation of the PMRI policy
- Assist with performance management and recommend initiatives to encourage employee retention
- Administer payroll functions such as timesheet collection, verification and calculations in order to meet payroll timelines
- Assist with creating and implementing the clinic health & safety policies and practices
- Review accident investigation reports to ensure appropriate internal and external reporting (including WSIB) is completed within required timeframes
- Participate in investigations as required
|
| Qualifications |
- University Degree with CHRP Designation
- Minimum 3 years in a HR Management role and 5-7 years HR experience
- Excellent diplomatic and conflict management skills
- Ability to work autonomously and maintain confidentiality is critical
- Above average problem solving skills
|
Apply in confidence to: jobs@pharmamedica.com
with Job #14803 indicated in the subject line
Applicants are thanked in advance for their interest however only
those candidates selected for an interview will be contacted.
All qualified candidates are encouraged to apply.
Pharma Medica is committed to a diversified workplace.
|
| Meal Preparation (Assistant) (Contract) |
| Approx 60 Hours Bi-Weekly (Part Time) @ Phase I Clinic (Toronto) |
| Updated: Friday, April 16, 2010 @ 3:47:00 PM |
| Job Summary |
| Provide essential dietary requirements for clinical studies following strict guidelines in relation to preparation methods and portion sizing for served meals. Variable shifts required from 5:30am to 10pm, 7 days per week |
| Duties |
|
| Qualifications |
|
Apply in confidence to: jobs@pharmamedica.com
with Job #19907 indicated in the subject line
Applicants are thanked in advance for their interest however only
those candidates selected for an interview will be contacted.
All qualified candidates are encouraged to apply.
Pharma Medica is committed to a diversified workplace.
|
| Meal Preparation (Supervisor) |
| 75 Hours Bi-Weekly (Full Time) @ Phase I Clinic (Toronto) |
| Updated: Thursday, July 23, 2009 @ 10:14:00 AM |
| Job Summary |
| Provide essential dietary requirements for clinical studies following strict guidelines in relation to preparation methods and portion sizing for served meals |
| Duties |
- Preparation of menus according to study protocol and instructions
- Follow proper requirements to ensure consistent and uniform meals
- Use proper food handling technique at all times
- Maintain a sanitary and organized food preparation and kitchen area
-
|
| Qualifications |
- Post-secondary education in food preparation an asset, Red Seal Certification preferred
- 2 years experience working in the food industry preferably within banquet halls, hospitals, or assisted living facilities
- Excellent English communication and writing skills
-
|
Apply in confidence to: jobs@pharmamedica.com
with Job #19806 indicated in the subject line
Applicants are thanked in advance for their interest however only
those candidates selected for an interview will be contacted.
All qualified candidates are encouraged to apply.
Pharma Medica is committed to a diversified workplace.
|
| Medical Results Coordinator |
| 75 Hours Bi-Weekly (Full Time) @ Phase I Clinic (Toronto) |
| Updated: Wednesday, June 30, 2010 @ 3:06:00 PM |
| Job Summary |
| To review and confirm subjects results and write summaries for all aspects of clinical studies. |
| Duties |
- Prepare complete subjects file (ensure lab results, ECGs) for review by MD (PI)
- Follow-up and resolve all screening repeat laboratory results
- Prepare summaries of medical issues for assessment of subjects eligibilities for future studies
- Ensure subject demographics obtained at recruitment is consistent with information obtain at medical screening
- Properly complete documentationi of clinical activities according to GCP, SOP, guidlines and applicable regulatory requirements
|
| Qualifications |
- University degree in Scientific discipline
- 1-2 years CRO experience / Medical Doctors office
- Excellent working knowledge of GLP/GCP
- Exceptional organizational and interpersonal skills
|
Apply in confidence to: jobs@pharmamedica.com
with Job #19103 indicated in the subject line
Applicants are thanked in advance for their interest however only
those candidates selected for an interview will be contacted.
All qualified candidates are encouraged to apply.
Pharma Medica is committed to a diversified workplace.
|
| Medical Screener (Contract) |
| Approx 60 Hours Bi-Weekly (Part Time) @ Phase I Clinic (Toronto) |
| Updated: Friday, July 09, 2010 @ 12:31:00 PM |
| Job Summary |
| Ensure that potential subjects meet the protocol requirement to ensure a full panel is obtained for each study |
| Duties |
- Obtain Informed Consent from prospective subjects by providing clear explanation of informed consent and answering questions or concerns of potential participants
- Perform screening procedures such as but not limited to: blood sample collection, sample processing and storage, vital signs, ECGs, etc., according to the study protocol and/or SOP requirements
- Properly complete documentation of clinical activities according to GCP, SOP guidelines, and/or FDA/TPD regulations
- Conduct initial interview with prospective subject and record subjects medical history
|
| Qualifications |
- 1 year working experience in a medical environment (clinic)
- 2-3 years CRO healthy adult screening experience OR foreign trained Medical Doctor
- Canadian MLA/MLT Certification and preferable OSMT certified
- Excellent verbal and written communication skills
- Must be willing to work shifts between 8am-8pm Monday-Saturday
|
Apply in confidence to: jobs@pharmamedica.com
with Job #19901 indicated in the subject line
Applicants are thanked in advance for their interest however only
those candidates selected for an interview will be contacted.
All qualified candidates are encouraged to apply.
Pharma Medica is committed to a diversified workplace.
|
| MLA (On Study) (Contract) |
| Approx 60 Hours Bi-Weekly (Part Time) @ Phase I Clinic (Toronto) |
| Updated: Friday, January 02, 2009 @ 1:57:00 PM |
| Job Summary |
| Perform sample collection on healthy adult volunteers, throughout the duration of our Clinical Trials, as per study requirements |
| Duties |
- Perform clinical tasks including study check-in procedures, blood sample collection, sample processing and sample storage
- Procure and/or process biological samples as required to conduct a clinical study
- Properly complete documentation of clinical activities according to GCP, SOP and FDA/TPD regulations
-
|
| Qualifications |
- Completion of a Canadian MLA/MLT program
- OSMT Certified (or working towards)
- 1 year CRO experience in catheter insertion & venipuncture
- Excellent communication skills and ability to multitask in a team-oriented environment
|
Apply in confidence to: jobs@pharmamedica.com
with Job #25803 indicated in the subject line
Applicants are thanked in advance for their interest however only
those candidates selected for an interview will be contacted.
All qualified candidates are encouraged to apply.
Pharma Medica is committed to a diversified workplace.
|
| MLA (Screening) (Contract) |
| Approx 60 Hours Bi-Weekly (Part Time) @ Phase I Clinic (Toronto) |
| Updated: Friday, April 09, 2010 @ 11:40:00 AM |
| Job Summary |
| Work with the Subject Selection & Recruitment team by aiding in the screening process of healthy adult volunteers |
| Duties |
- Perform volunteer screening procedures in order to prepare for Clinical Trials
- Ensure sufficient numbers of screened volunteers for Phase I studies
- Complete medical background checks to confirm volunteer eligibility
- Ensure proper documentation of clinical activities
|
| Qualifications |
- Completion of a Canadian MLA/MLT program
- OSMT Certified (or working towards)
- 1 year CRO experience in phlebotomy
- Excellent communication skills and ability to multitask in a team-oriented environment
-
|
Apply in confidence to: jobs@pharmamedica.com
with Job #19807 indicated in the subject line
Applicants are thanked in advance for their interest however only
those candidates selected for an interview will be contacted.
All qualified candidates are encouraged to apply.
Pharma Medica is committed to a diversified workplace.
|
| QC Assoc. (Clinic) / Clinical Data Reviewer |
| 75 Hours Bi-Weekly (Full Time) @ Phase I Clinic (Toronto) |
| Updated: Thursday, April 01, 2010 @ 2:11:00 PM |
| Job Summary |
| Ensure all prepared clinical trails phase I study source documentation is complete and in accordance to protocols, PMRI SOPs and regulations |
| Duties |
- Assist in the review of study files upon data entry at check-in, on-study and post-study procedures
- Observe the clinical procedures during the conduct of studies and make sure that they are performed in accordance to protocols, PMRI SOPs, GCP and regulations (i.e. screening procedures, subject entrance, meals, sample bundling, etc.)
- Ensure that study files after study completion are accurate and legible according to protocols, PMRI SOPs, GCP and regulations
- Assist in the review of other study related documentation (i.e. pharmacy records)
|
| Qualifications |
- B.Sc. in Health Sciences or equivalent
- Pharmaceutical RA/QA/QC (post grad program) or knowledge of GCP
- 1-2 years CRO experience
- Computer software knowledge
- Ability to communicate clearly and effectively with staff and subjects
- Exceptional organizational skills
|
Apply in confidence to: jobs@pharmamedica.com
with Job #18801 indicated in the subject line
Applicants are thanked in advance for their interest however only
those candidates selected for an interview will be contacted.
All qualified candidates are encouraged to apply.
Pharma Medica is committed to a diversified workplace.
|
| Quality Assurance Associate (Clinic) |
| 75 Hours Bi-Weekly (Full Time) @ Phase I Clinic (Toronto) |
| Updated: Thursday, September 10, 2009 @ 2:01:00 PM |
| Job Summary |
| Performs audits of Phase 1 Clinical Trials ensuring compliance according to ICH-GCP, Health Canada Food and Drug Regulations Division 5, applicable regulatory guidelines, and corporate SOPs |
| Duties |
- Perform audits of Clinical study activities (i.e. dosing, blood sample collection, sample processing) for compliance with GCP, applicable guidelines, regulations, protocols and SOPs
- Perform audits of Clinical study documentation (i.e. pre-study, end of study, pharmacy records) for compliance with GCP, applicable guidelines, regulations, protocols and SOPs
- Report findings to Management
- Ensure effective follow-up and resolution of audit findings
- Monitor corrective actions
|
| Qualifications |
- Post-Secondary education in a related discipline such as Scientific or Pharmaceutical
- 2-3 years experience auditing clinical trials or related Phase 1 Clinic experience
- Exceptional proficiency with ICH Good Clinical Practice
- Excellent organizational and interpersonal skills
- Meticulous and very detail oriented
- This position requires shift/weekend work
|
Apply in confidence to: jobs@pharmamedica.com
with Job #13805 indicated in the subject line
Applicants are thanked in advance for their interest however only
those candidates selected for an interview will be contacted.
All qualified candidates are encouraged to apply.
Pharma Medica is committed to a diversified workplace.
|
| Receptionist |
| Approx 60 Hours Bi-Weekly (Part Time) @ Phase I Clinic (Toronto) |
| Updated: Thursday, July 23, 2009 @ 10:37:00 AM |
| Job Summary |
| Responsible for maintaining a professional environment when answering calls and greeting arrivals at PMRI Phase I Clinic. Variety of Shifts and positions currently open. |
| Duties |
- Answering multi-line phone system
- General office duties including taking phone messages and photocopying
- Screen all inbound telephone calls
- Greeting customers and volunteers
- Ability to communicate clearly and effectively with all members of the PMRI team and visitors/volunteers
- Maintaining the high standards of a client services oriented company
- Exceptional organizational skills
|
| Qualifications |
- College Diploma or Certificate and/or formalized training in a related field
- Polite interpersonal skills and ability to work effectively in a team environment
- Computer skills
- Ability to work and cover varied shifts from 6am to 10pm 7 days a week
|
Apply in confidence to: jobs@pharmamedica.com
with Job #17805 indicated in the subject line
Applicants are thanked in advance for their interest however only
those candidates selected for an interview will be contacted.
All qualified candidates are encouraged to apply.
Pharma Medica is committed to a diversified workplace.
|
| Recruiter (Contract) |
| Approx 60 Hours Bi-Weekly (Part Time) @ Phase I Clinic (Toronto) |
| Updated: Wednesday, August 25, 2010 @ 9:03:00 AM |
| Job Summary |
| Recruit and inform potential subjects of upcoming studies. Must be willing to work shifts between 8:00am and 8:00pm Monday to Saturday, Sunday 11:00am to 5:00pm |
| Duties |
- Recruitment of subjects using Clinic Subject Eligibility Database
- Telephone screening of subjects and documenting conversations regarding their medical history
- Providing subjects with the correct information by phone
|
| Qualifications |
- Excellent communication skills
- Excellent interpersonal skills and telephone manner
- Minimum of one year CRO experience
- Minimum B.Sc. or related degree/diploma
- Must be willing to work shifts between 8am-8pm Monday-Saturday
|
Apply in confidence to: jobs@pharmamedica.com
with Job #19802 indicated in the subject line
Applicants are thanked in advance for their interest however only
those candidates selected for an interview will be contacted.
All qualified candidates are encouraged to apply.
Pharma Medica is committed to a diversified workplace.
|
| Recruiting Training Coordinator |
| 75 Hours Bi-Weekly (Full Time) @ Phase I Clinic (Toronto) |
| Updated: Thursday, May 22, 2008 @ 10:59:00 AM |
| Job Summary |
| Responsible for the initial and on-going training of our CSR staff in our Subject Recruitment Centre |
| Duties |
- Responsible for training all new Customer Service Representatives regarding recruiting procedures and documentation
- Responsible for the on-going training of the CSR’s during their employment
- Ensure CSR’s are regularly updated in keeping with SOP, GCP and regulatory guidelines for each specific task and documentation of each task as per their job function
- Supervise and/or perform all technical functions: recruiting volunteers, updating subject files in CESR, create new study files in CESR, screening reception procedure, auditing CESR study files in compliance with protocol, SOPs and GCP and conduct protocol meeting with CSR’s prior to new study recruiting
- Advise superiors on possible improvements in the recruiting procedures, clinical documentation practices and in performance of staff
|
| Qualifications |
- B.Sc or suitable related experience
- At least one year experience training in a Contract Research Organization
- Call centre experience
- Excellent knowledge of SOPs and GCP requirement
|
Apply in confidence to: jobs@pharmamedica.com
with Job #19804 indicated in the subject line
Applicants are thanked in advance for their interest however only
those candidates selected for an interview will be contacted.
All qualified candidates are encouraged to apply.
Pharma Medica is committed to a diversified workplace.
|
| Screening Clinical Data Reviewer |
| 75 Hours Bi-Weekly (Full Time) @ Phase I Clinic (Toronto) |
| Updated: Friday, June 11, 2010 @ 11:21:00 AM |
| Job Summary |
| Review all screening and study files generated from subject selection to ensure compliance with Phase I Clinical Studies |
| Duties |
- Ensure that all screening files for each study are accurate and legible according to the study protocol and relevant SOPs
- Ensure accurate preparation of screening Case Report Forms (CRFs)
- Assist in the review of study files upon data entry at recruiting
- Provide report on the reviewed data to the supervisor of the study and follow-up upon resolution
- Interact with other departments to improve the accuracy and quality of data
- Ensure proper documentation of clinical activities according to SOP, GCP, TPD, FDA or other regulatory agency guidelines
|
| Qualifications |
- Post Graduate education in a related discipline (QC/QC/RA)
- Bachelors of Science (preferred)
- Knowledgeable in the interpretation of clinic data
- Excellent understanding of Phase I study protocols and conduct
- Ability to communicate clearly and effectively with staff and subjects
- Must be willing to work shifts between 8am-7pm Monday-Saturday
|
Apply in confidence to: jobs@pharmamedica.com
with Job #19803 indicated in the subject line
Applicants are thanked in advance for their interest however only
those candidates selected for an interview will be contacted.
All qualified candidates are encouraged to apply.
Pharma Medica is committed to a diversified workplace.
|
| Screening Coordinator (Assistant) |
| 75 Hours Bi-Weekly (Full Time) @ Phase I Clinic (Toronto) |
| Updated: Thursday, July 23, 2009 @ 10:32:00 AM |
| Job Summary |
| Assist with the overall organizational and planning efforts needed in order to prepare for Phase I clinical trials |
| Duties |
- Assist in all aspects of the screening process in compliance with protocol specific guidelines and regulations (SOP, GCP, FDA and other regulatory agencies)
- Assist and/or perform technical functions such as screening consent, and other clinical tasks to generate data
- Ensure sufficient number of qualified subjects for Phase I studies and proper preparation of screening documents
|
| Qualifications |
- Bachelor of Science in a related field
- 1 year Post-Graduate training in the pharmaceutical field an asset
- 1 year Phase I CRO experience an asset
- Proficient English verbal and written skills
- Excellent computer skills
|
Apply in confidence to: jobs@pharmamedica.com
with Job #19805 indicated in the subject line
Applicants are thanked in advance for their interest however only
those candidates selected for an interview will be contacted.
All qualified candidates are encouraged to apply.
Pharma Medica is committed to a diversified workplace.
|
| Screening Nurse |
| 75 Hours Bi-Weekly (Full Time) @ Phase I Clinic (Toronto) |
| Updated: Thursday, September 18, 2008 @ 9:23:00 AM |
| Job Summary |
| Supervise and/or perform all aspects of the screening process in compliance with protocol specific requirements, SOP, GCP, FDA, TPP or other relevant regulatory agency guidelines |
| Duties |
- Answer technical questions from medical screeners, MLA and/or subjects
- Follow up with subjects for any abnormal medical results
- Address queries from Toronto Public Health regarding reportable diseases
|
| Qualifications |
- Bachelors of Nursing required
- Ability to communicate clearly and effectively with other staff and subjects
- Exceptional organizational skills
|
Apply in confidence to: jobs@pharmamedica.com
with Job #19801 indicated in the subject line
Applicants are thanked in advance for their interest however only
those candidates selected for an interview will be contacted.
All qualified candidates are encouraged to apply.
Pharma Medica is committed to a diversified workplace.
|
| Study Coordinator / Study Coordinator (Assistant) |
| 75 Hours Bi-Weekly (Full Time) @ Phase I Clinic (Toronto) |
| Updated: Thursday, July 23, 2009 @ 10:33:00 AM |
| Job Summary |
| Supervise and coordinate the planning of clinical studies |
| Duties |
- Supervising and planning the timely execution of clinical studies
- Ensure all study documentation is accurate, current, and complete according to study protocol, SOP, GCP, and regulatory guidelines
- Generate study summary based on protocol
- Supervise and/or perform all technical functions: phlebotomy, ECG, vital signs and other clinical tasks to generate data in compliance with protocol, SOP and GCP
- Ensuring subject safety by monitoring and documenting Adverse Events
- Conduct pre-study protocol review meetings as necessary of study activities for technical team
- Coordinate transcription of raw data onto CRFs
- Performing final review of study documentation, ensuring accuracy according to protocol, SOP and GCP
- Resolving conflicts among subjects and address subjects concerns
|
| Qualifications |
- Masters Degree (preferable within Science) with knowledge of conducting clinical trials
- Working knowledge of Phase I study protocols and conduct
- Understanding of the value of training and SOP relating to study conduct GCP training
- Excellent computer skills
- Ability to communicate clearly and effectively with direct reports and other clinical staff
- Exceptional organizational skills
|
Apply in confidence to: jobs@pharmamedica.com
with Job #17802 indicated in the subject line
Applicants are thanked in advance for their interest however only
those candidates selected for an interview will be contacted.
All qualified candidates are encouraged to apply.
Pharma Medica is committed to a diversified workplace.
|
| Study Nurse |
| Approx 60 Hours Bi-Weekly (Part Time) @ Phase I Clinic (Toronto) |
| Updated: Thursday, April 01, 2010 @ 11:41:00 AM |
| Job Summary |
| Supervise and perform all aspects of the clinical trials process in compliance with protocol specific requirements and relevant regulatory agency guidelines.
Shifts required 7 days a week 6:00 am - 10:00 pm. |
| Duties |
- Dispense and use the investigational products in accordance with the approved protocol
- Explain the correct use of the investigational product to the subjects, and ensure that the subjects are following the instructions properly
- Administer investigational products for the conduct of a clinical study, as well as any concomitant medication under the supervision/order of the investigator
- Ensure health and safety of the subjects by performing medical checks (e.g. medical history, vital signs, electrocardiograms) and health monitoring
|
| Qualifications |
- Bachelors of Nursing required (B.Sc.N.)
- Ability to communicate clearly and effectively with other staff and subjects
- Exceptional organizational skills
|
Apply in confidence to: jobs@pharmamedica.com
with Job #17900 indicated in the subject line
Applicants are thanked in advance for their interest however only
those candidates selected for an interview will be contacted.
All qualified candidates are encouraged to apply.
Pharma Medica is committed to a diversified workplace.
|
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