Toronto On Clinical research volunteer Jobs – 227 Openings This Week

Study Coordinator - Clinical Research
Pharma Medica Research Inc. —Toronto, ON
- $50,000–$55,000 a year
- Full-time
- Vital signs
- Medication administration
- English
Quick apply
Research Assistant (SRI) - Evaluative Clinical Sciences - Casual - 2026-18669
Sunnybrook Health Sciences Centre —Toronto, ON
- Doctoral degree
- Master's degree
- Bachelor's
Quick apply
4d
High School Intern (SRI) - Evaluative Clinical Sciences - Temporary Part-Time 2026-17699
Sunnybrook Health Sciences Centre —Toronto, ON
- Temporary
- Databases
- High school diploma or GED
- Communication skills
Quick apply
Clinical Research Coordinator (SRI) - Evaluative Clinical Sciences - Regular Full-Time 2026-18503
Sunnybrook Health Sciences Centre —Toronto, ON
- Full-time
- Master's degree
- Bachelor's
- Psychology
Quick apply
Clerical Support Associate - OP Mental Health
Humber River Health —Greater Toronto Area, ON
- $29.97–$31.02 an hour
- 8 hour shift
- Computer literacy
- Microsoft Office
- High school diploma or GED
Clerical Support Associate, Bariatric
Humber River Health —Greater Toronto Area, ON
- $29.97–$31.02 an hour
- Temporary
- High school diploma or GED
- Organizational skills
- Typing
Clerical Support Associate, Birthing Unit
Humber River Health —Toronto, ON
- $29.97–$31.02 an hour
- Temporary
- Computer literacy
- Microsoft Office
- Administrative experience
Research Associate
Humber River Health —Greater Toronto Area, ON
- $49.91–$62.43 an hour
- Temporary
- Microsoft Powerpoint
- Microsoft Word
- Microsoft Outlook
4d
Clerical Support Associate Mother Baby Unit
Humber River Health —Greater Toronto Area, ON
- $29.97–$31.02 an hour
- Temporary
- High school diploma or GED
- Typing
- Medical terminology
Health Information Services Clerk
Humber River Health —Greater Toronto Area, ON
- $28.09–$29.09 an hour
- 8 hour shift
- Computer literacy
- English
- Microsoft Office
Staffing Resource Centre Assistant
Humber River Health —Greater Toronto Area, ON
- $31.74–$39.69 an hour
- Full-time
- Microsoft Access
- Microsoft Outlook
- Administrative experience
13d
Clinical Coordinator - Infection Control
Humber River Health —Greater Toronto Area, ON
- $52.79–$66.03 an hour
- Part-time
- Microsoft Powerpoint
- Microsoft Word
- Nursing
4d
Unit Aide - Emergency
Humber River Health —Greater Toronto Area, ON
- $27.76–$28.31 an hour
- Temporary
- English
- High school diploma or GED
- Cleaning
Pharmacist
Humber River Health —Greater Toronto Area, ON
- $48.21–$64.50 an hour
- Temporary
- Bachelor's
- Team management
- Travel
Nurse Practitioner
Unison Health and Community Services —Toronto, ON
- $67.66–$77.21 an hour
- Part-time
- Computer literacy
- Research
- Patient care
- Paid time off
Quick apply
5d
Registered Orthopaedic Technologist, Senior - Ambulatory Care, U (J0725-0844)
North York General Hospital —Toronto, ON
- $37.06–$42.91 an hour
- Weekends as needed
- High school diploma or GED
- Mentoring
- Leadership
Quick apply
Psychologist - CMH-Eating Disorder, FT (J0226-0690)
North York General Hospital —Toronto, ON
- $70.07–$84.42 an hour
- 8 hour shift
- Doctoral degree
- English
- Research
Quick apply
Sonographer, Cardiac - Cardio Resp & Neuro Diagnostics, FTT (J0726-0484 )
North York General Hospital —Toronto, ON
- $43.75–$52.71 an hour
- Temporary
- CPR Certification
- English
- Microsoft Office
Quick apply
Director, Clinical Diagnostics - FT (J0826-0603)
North York General Hospital —Toronto, ON
- $167,568.57–$201,889.55 a year
- 8 hour shift
- Customer service
- Finance
- Master's degree
Quick apply
14d
Recreation Therapist - CVH 2 Critical Care (Long Stay Program)
Mackenzie Health —Vaughan, ON
- $37.23–$43.53 an hour
- Temporary
- Hybrid work
- BLS Certification
- English
- Communication skills

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Study Coordinator - Clinical Research

Pharma Medica Research Inc. -
Toronto, ON

Quick apply

Job details

Full-time
$50,000–$55,000 a year

Qualifications

Computer operation
Specimen collection
Vital signs
Medication administration
Clinical research
Informed consent
Case file maintenance
EKG
Filing
English
Technical support
Master's degree
Transcription
Bachelor's
Team management
Data entry
Organizational skills
Good Clinical Practice (GCP)
Standard operating procedures (SOPs)
Communication skills
Team coordination

Full job description

Pharma Medica Research is a full service contract research organization specialized in conducting early phase clinical trails in healthy volunteers, special and patient populations. We are currently looking for a Study Coordinator to join our clinic location in Scarborough.

The function of the Study Coordinator I is to plan the study activities under the supervision of the Study Coordinator II. Assist, and when necessary, supervise and/or perform all technical functions required to generate data in compliance with protocols, Pharma Medica Research Inc.'s (PMRI's) SOPs, GCP requirements and other regulatory guidelines. Be aware at all times of the human safety factors. Ensure that procedures are performed in a timely manner. Answer technical questions from technicians. Monitor adverse events. Assist in the supervision and direction of technical staff on study in terms of performance of functions. This position reports to the Manager, Clinical Operations and/or designate.

Duties and Responsibilities

Plan and supervise the timely execution of studies under the supervision of the Study Coordinator II.
Generate a study summary based on the protocol.
Ensure that regulatory documents like FDF, FDA 1572, QIU, ERB Letter of Approval, NOL, etc. are available prior to study check-in.
Coordinate the ordering of study-specific materials to conduct clinical studies.
Conduct pre-study protocol review meetings for the technical team.
Ensure that the study schedule is prepared in compliance with the study requirements.
Communicate with the Study Preparation Coordinator and the QC unit to ensure that appropriate CRFs are prepared prior to study check-in.
Liaise with the Screening department to ensure that queries pending at check-in are addressed prior to drug administration.
Ensure that the study drugs are received prior to study conduction.
Communicate with the Principal Investigator to ensure that an Investigator is present to perform the necessary physical examination and monitoring procedures.
Ensure that the ICF is provided to the subjects, answer any questions the subjects may have regarding the protocol and Informed Consent, and sign the Informed Consent forms.
Supervise and when required, assist and/or perform all technical functions: phlebotomy, ECG, vital signs and other clinical tasks to generate data in compliance with protocol, SOPs and GCP requirements.
Perform safety-related procedures as required (e.g. conducting vital signs, electrocardiograms, concomitant medication administration) and health monitoring.
Assist or administer certain types of investigational products as required for the conduct of a clinical study under the supervision/order of the investigator.
Ensure subject safety by timely documenting and following-up on Adverse Events.
Ensure all study documentation is accurate, current, and complete according to study protocol, SOPs, GCP, and other regulatory guidelines.
Coordinate with the Project Management department regarding study related issues and project deadlines.
Assist in resolving conflicts among subjects and address subjects' concerns.
Generate client updates and forward to the Project Management department as required.
Coordinate with the accounting department regarding study subjects' compensation.
Ensure the timely shipping of the clinical and analytical samples.
Assist in performing final review of study documentation, ensuring accuracy according to protocol, SOPs and GCP, and other regulatory guidelines.
Ensure timely completion of deviation forms as needed.
Ensure timely receipt and review of post-study laboratory reports.
Ensure timely completion of the study files according to project deadlines.
Address queries and audit findings from QC and QA.
Coordinate the transcription of raw data onto CRFs where necessary.
Update the subjects' files for outstanding follow-ups, subjects' behavior issues, non-compliance, etc.
Other duties as required.

Qualifications:

Minimum B.Sc. degree with 1 year experience in conducting clinical trials or;
M.Sc. degree with adequate knowledge of conducting clinical trials.
Working knowledge of Phase I study Protocols and conduct.
GCP training.
Proficiency in computer usage and software applications.
Excellent communication skills including excellent English verbal and written skills.
Ability to communicate clearly and effectively with direct reports and other clinical staff.
Excellent interpersonal skills.
Ability to work both independently and as a team member.
Flexibility with changes in working schedules/shifts.
Exceptional organizational skills

We Offer

Competitive compensation plan
Opportunities for advancement and career progression
A generous Employee Milestones Awards Program
Corporate Discounts Program
Learning Support Programs
Friendly atmosphere, culture of learning

Salary Range is between $50,000 - $55,000/year

Please note all applications must be eligible to work within Canada.

PMRI is an Equal Opportunity Employer; promoting accessibility and inclusivity at work and offering accommodation for applicants as required and requested.

We thank all applicants for their interest; however, only those selected to proceed in the interview process will be contacted.

If you meet the qualifications and are looking for an exciting place to work, apply today!

If interested in this position, apply today!

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Refine Your Search

clinical research volunteer jobs in toronto on

Study Coordinator - Clinical Research

Research Assistant (SRI) - Evaluative Clinical Sciences - Casual - 2026-18669

High School Intern (SRI) - Evaluative Clinical Sciences - Temporary Part-Time 2026-17699

Clinical Research Coordinator (SRI) - Evaluative Clinical Sciences - Regular Full-Time 2026-18503

Clerical Support Associate - OP Mental Health

Clerical Support Associate, Bariatric

Clerical Support Associate, Birthing Unit

Research Associate

Clerical Support Associate Mother Baby Unit

Health Information Services Clerk

Staffing Resource Centre Assistant

Clinical Coordinator - Infection Control

Unit Aide - Emergency

Pharmacist

Nurse Practitioner

Registered Orthopaedic Technologist, Senior - Ambulatory Care, U (J0725-0844)

Psychologist - CMH-Eating Disorder, FT (J0226-0690)

Sonographer, Cardiac - Cardio Resp & Neuro Diagnostics, FTT (J0726-0484 )

Director, Clinical Diagnostics - FT (J0826-0603)

Recreation Therapist - CVH 2 Critical Care (Long Stay Program)

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