Etobicoke, On Paid research participant Jobs – 76 Openings This Week

Principal Investigator
MPA Recruitment Canada Ltd —Toronto, ON
- $350,000–$500,000 a year
- Full-time
- Medicine
- Doctoral degree
- In-person
- Dental care
- Paid time off
Quick apply
Child Care Educator (RECE, CYW, OCT, Rec & Leisure, SSW, ECA)
YMCA of Greater Toronto —Etobicoke, ON
- $22–$28 an hour
- Temporary
- CPR Certification
- English
- High school diploma or GED
- Dental care
- Paid time off
1d
Child Care Educator (RECE, CYW, OCT, Rec & Leisure, SSW, ECA)
YMCA of Greater Toronto —Etobicoke, ON
- $22–$28 an hour
- Temporary
- CPR Certification
- English
- High school diploma or GED
- Dental care
- Paid time off
1d
Business Development Representative
Prepr —Toronto, ON
- $60,000–$75,000 a year
- Full-time
- Hybrid work
- CRM software
- Microsoft Excel
- Sales
- Dental care
- Paid time off
Quick apply
Senior Developer (Full-stack)
Solutions Petal Inc. —Toronto, ON
- Full-time
- Remote
- Azure
- Databases
- AWS
- Flexible schedule
Quick apply
17h
Solutions Analyst
CanDeal —Toronto, ON
- $47,142.72–$92,242.69 a year
- Full-time
- Hybrid work
- Microsoft Powerpoint
- Microsoft Word
- Microsoft Excel
- Dental care
- Paid time off
Quick apply
23h

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Principal Investigator
MPA Recruitment Canada Ltd —Toronto, ON
At least 8 years of experience in drug development and clinical trial administration, with active clinical practice in a relevant therapeutic area.
$350,000–$500,000 a year
Quick apply
Community & Events Fundraising Manager
Children Believe Fund —Markham, ON
This position requires strong fundraising, organizational and logistical skills, but more importantly, the ability to build and develop relationships with the…
$64,000–$75,000 a year
Quick apply
5d

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paid research participant jobs near etobicoke, on

Principal Investigator

MPA Recruitment Canada Ltd -
Toronto, ON

Quick apply

Job details

Permanent | Full-time
$350,000–$500,000 a year

Qualifications

Medicine
Doctoral degree

Full job description

Principal Investigator
Toronto / Greater Toronto Area

MPA are retained by a Toronto based CRO to recruit for a Principal Investigator to join their team. The CRO run early-phase studies, bioequivalence testing, validate new drugs and provide regulatory support for pharmaceutical companies.

In this role, you will uphold Good Clinical Practice (GCP) by ensuring protocol compliance, protecting participant welfare, maintaining data integrity, and overseeing clinical investigations in line with regulatory requirements.

Duties and Responsibilities:

Conduct clinical trials in accordance with the approved protocol, including any amendments, as well as all study procedures and directives
Protect the rights, safety, and well-being of all participants, ensuring appropriate medical care throughout their involvement in the trial
Maintain thorough knowledge of investigational product(s) as outlined in the protocol, Investigator’s Brochure, and product monograph, and provide clear instructions to participants on proper use
Adhere to study randomization procedures and promptly document and report any premature unblinding to the sponsor and IRB, where applicable
Obtain and properly document informed consent in compliance with all regulatory and ethical requirements
Report all Serious Adverse Events (SAEs) and pregnancy notifications to the sponsor and IRB in a timely manner
Assess participant eligibility and ongoing health status, including medical history, inclusion/exclusion criteria, laboratory results, vital signs, adverse events, and study-specific procedures
Evaluate adverse events for causality, severity, and outcome, and recommend follow-up actions, including repeat testing when clinically indicated
Perform physical examinations of study participants
Confirm participant eligibility for investigational product administration
Follow up on clinically significant findings, including positive infectious disease results and notify appropriate health authorities as required
Ensure site compliance with Good Clinical Practice (GCP), standard operating procedures (SOPs), and applicable regulatory requirements
Review and sign clinical trial protocols, clinical study reports, and case report forms (as applicable), and participate in safety data reviews when required
Maintain accurate, complete, and legible study records, ensuring availability for review by monitors, auditors, and regulatory authorities.

Qualifications:

· Medical Doctor (M.D.) degree

· Registered and in good standing with CPSO.

· Minimum of 5 years of experience in clinical research

· At least 8 years of experience in drug development and clinical trial administration, with active clinical practice in a relevant therapeutic area

· Demonstrated ability to adapt to changing priorities and manage multiple projects effectively

· Advanced and up-to-date knowledge of:

o Clinical trials and study design

o Drug development processes

o Medical monitoring

o Applicable federal and international regulations and guidelines

· Familiarity with medical coding systems and adverse event review/reporting processes is considered an asset

Strong compensation package on offer. If this opportunity would be of interest to you, please reach out to [email protected] for a confidential chat.

Pay: $350,000.00-$500,000.00 per year

Benefits:

Dental care
Extended health care
Life insurance
Paid time off
Stock options

Work Location: In person

Quick apply

Refine Your Search

paid research participant jobs in etobicoke, on

Principal Investigator

Child Care Educator (RECE, CYW, OCT, Rec & Leisure, SSW, ECA)

Child Care Educator (RECE, CYW, OCT, Rec & Leisure, SSW, ECA)

Business Development Representative

Senior Developer (Full-stack)

Solutions Analyst

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