Markham, On Lead clinical research associate Jobs – 38 Openings This Week

Clinical Research Associate II (SRI) - Odette Cancer Centre Clinical Trials - Regular Full-Time 2026-17987
Sunnybrook Health Sciences Centre —Toronto, ON
- Full-time
- Laboratory experience
- Microsoft Office
- Databases
- Paid time off
Quick apply
12d
Clinical Research Associate - Canada
サイネオス・ヘルス —Toronto, ON
- Presentation skills
- Bachelor's
- Travel
Experienced Clinical Research Associate - Sponsor Dedicated
サイネオス・ヘルス —Toronto, ON
- Presentation skills
- Bachelor's
- Travel
- Employee stock purchase plan
- Dental care
Clerical Support Associate Prenatal Obstetrical Clinic
Humber River Health —Greater Toronto Area, ON
- $29.97–$31.02 an hour
- Temporary
- High school diploma or GED
- Computer skills
- Typing
14d
Sr. Clinical Operations Lead (Clinical Trial Manager)
Alimentiv —Toronto, ON
- $78,000–$130,000 a year
- Full-time
- Remote
- Microsoft Office
- Bachelor's
- Organizational skills
Quick apply
Clerical Support Associate Birthing Unit
Humber River Health —Toronto, ON
- $29.97–$31.02 an hour
- Temporary
- Microsoft Office
- Administrative experience
- High school diploma or GED
Therapeutic Area Lead, Specialty Care
AbbVie —Toronto, ON
- Full-time
- Hybrid work
- Microsoft Powerpoint
- Microsoft Word
- Medicine
9d
Bilingual Sr. Clinical Research Associate
Alimentiv —Toronto, ON
- $78,000–$130,000 a year
- Full-time
- Remote
- Bilingual
- English
- Travel
Quick apply
Clerical Support Associate, Fracture Clinic
Humber River Health —Greater Toronto Area, ON
- $29.11–$30.13 an hour
- Temporary
- Customer service
- High school diploma or GED
- Organizational skills
14d
Clerical Support Associate, Bariatric
Humber River Health —Greater Toronto Area, ON
- $29.97–$31.02 an hour
- Temporary
- Customer service
- High school diploma or GED
- Organizational skills
5d
Clerical Support Associate, Surgical Prescreening
Humber River Health —Toronto, ON
- $29.97–$31.02 an hour
- Temporary
- Customer service
- High school diploma or GED
- Organizational skills
Clerical Support Associate - OP Mental Health
Humber River Health —Greater Toronto Area, ON
- $29.97–$31.02 an hour
- 8 hour shift
- Customer service
- Microsoft Office
- High school diploma or GED
14d
Clerical Support Associate, Operating Room
Humber River Health —Greater Toronto Area, ON
- $29.97–$31.02 an hour
- Temporary
- Customer service
- Microsoft Office
- High school diploma or GED
Clerical Support Associate, Birthing Unit
Humber River Health —Toronto, ON
- $29.97–$31.02 an hour
- Temporary
- Microsoft Office
- Administrative experience
- High school diploma or GED
2d
Program Implementation Specialist
Bayshore HealthCare —Markham, ON
- $54,000–$67,500 a year
- Full-time
- Remote
- PMP
- Business development
- Project management
Clerical Support Associate, Emergency Department, Part time
Humber River Health —Greater Toronto Area, ON
- $29.97–$31.02 an hour
- 8 hour shift
- Customer service
- Microsoft Office
- High school diploma or GED
4d
Clinical Operations & Enablement Lead
Nucs AI —Toronto, ON
- Full-time
- Hybrid work
- Master's degree
- Presentation skills
- Bachelor's
Quick apply
Scientific Associate - Pre-clinical Research
CAMH —Toronto, ON
- $93,822.73–$140,734.09 a year
- Full-time
- Computer science
- Doctoral degree
- Computer Science
1d
Associate Director, Medical Programs
Nucs AI —Toronto, ON
- Full-time
- Hybrid work
- Laboratory experience
- Research
- Master's degree
Quick apply
Clerical Support Associate, Post Anesthesia Care Unit (PACU)
Humber River Health —Greater Toronto Area, ON
- $29.97–$31.02 an hour
- Part-time
- Customer service
- High school diploma or GED
- Organizational skills
2d

I want to receive the latest job alerts for lead clinical research associate in markham, on

By signing in to your account, you agree to SimplyHired's Terms of Service and consent to our Cookie and Privacy Policy.

Explore jobs in more locations

lead clinical research associate jobs near markham, on

Clinical Research Associate II (SRI) - Odette Cancer Centre Clinical Trials - Regular Full-Time 2026-17987

Sunnybrook Health Sciences Centre -
Toronto, ON

Quick apply

Job details

Full-time
12 days ago

Qualifications

College certificate
Laboratory experience
Microsoft Office
Databases
Analysis skills
Bachelor's
Dangerous goods
Contracts
Communications
College diploma
Medical terminology
Communication skills
Time management

Full job description

Summary of Duties and Responsibilities:

The Odette Cancer Center (OCC) Clinical Research program is part of Sunnybrook Research Institute’s (SRI) ongoing commitment to participate in innovative and high quality clinical research.

Within OCC Clinical Research, the Clinical Trials Manager and Budget & Operations Coordinator, work with 35+ physicians actively participating in clinical research and 55+ OCC clinical research disease site-specific staff. Our program is comprised of 12 disease site groups; Breast, CNS, NETS, GI, GU medical, GU radiation, Gynecology, Head & Neck, Hematology, Lung, Melanoma and Early Phase I-II trials; as well as the pan-Canadian initiative, Canadian Cancer Clinical Trials Network (3CTN).

The goal of this position is to assist the GU Med Oncology Disease Site Group with the maintenance of their active oncology clinical research studies, databases, and trials. This position is for a full-time position working weekdays on-site at Sunnybrook, Bayview campus. This position is entitled to health benefits plan, pension, and paid time off/sick days. The CRA II will report to the team Physician Site Lead, team Supervisor, and PIs. The CRA II may also work closely with an interdisciplinary team including the Clinical Trials Manager, Operation Leads, and all other OCC Clinical Research Program staff.

Primary responsibilities include but are not limited to:

Independently lead the management of several complex Health Canada-regulated interventional clinical trials, academic clinical trials, and other research projects
Requesting, handling, and/or processing laboratory specimens (blood, urine, tissue)
Consenting patients, reviewing trial eligibility criteria and medical records
Applying clinical trial protocol requirements into patient & data activities such as documenting medical history, medications and adverse events from patients; reporting Serious Adverse Events
Scheduling and conducting patient appointments, completing qualify of life questionnaires with patients
Conducting measurements on patients including vital signs, ECGs, height/weight measurements
Communication with various hospitals and health service facilities to obtain medical information

Understanding requirements of the ethics review process, completing REB submissions and documentation updates
Data entry and resolving sponsor queries
Scheduling and participating in monitoring visits, sponsor audit visits, regulatory inspections
Maintaining documentation as part of the trial master file, creating source documents
Communication with internal hospital departments or liaising with Contract Research Organizations (CROs) and Sponsors/Trial Lead hospitals on behalf of your principal investigators
Tracking of trial metrics, and other research-related activities within the needs of the team
Leading the activation activities of new clinical trials with external sponsors and CROs, and the closure of completed trials

The successful candidate will be an eager team player who meets the following qualifications/skills:

Research Qualifications/Skills:

Requires the successful minimum completion of a Community College Diploma/Certificate or University Degree in a health related discipline
A minimum of 3-5 years of related professional or practical experience, including at least 3 years in clinical research, or the equivalent combination of education and professional experience; Health Canada-regulated clinical trial experience preferred
SoCRA/CCRP certification an asset; oncology clinical trial experience an asset
In-depth knowledge of ICH guidelines, Good Clinical Practice, and transportation of dangerous goods
Proven experience in processing and shipping blood samples
Experience in the informed consent process and working directly with research participants
Ability to understand and apply clinical trial protocols and laboratory manuals
Knowledge and experience in the ethics review and submission process
Strong working capability of MS Office and ability to quickly adapt to new online systems and applications, accurately entering data, and resolving queries (EDC databases, document portals)
Experience maintaining clinical trial documentation in a Trial Master File, creating source documentation
Experience in patient-facing communication, including obtaining AE/SAE or other trial-related medical information
Familiarity with medical terminology or experience reviewing patient health records
Experience or familiarity with research contracts and budget management an asset
May be involved in training new team members or assisting junior staff on team

Interpersonal Qualifications/Skills:

Well-developed organizational and time management skills
Excellent team work with a strong “can-do” attitude to build working relationships
Excellent oral and written communication skills; using professional communication tactics across multidisciplinary teams and external stakeholders
Ability to follow verbal instruction, written procedures, and apply trainings in practice
Demonstrated accurate and efficient work habits with close attention to detail and high quality of work
Strong analytical skills and ability to apply critical thinking for complex problem solving independently
Reliable attendance and punctuality
Strong accountability for independent workload; maintain multiple projects with minimal direct supervision; develop and maintain tools or trackers to enhance task performance
Demonstrated professional behaviours and ethical integrity
Strong cultural competency and ability to work respectfully in diverse team environments

Interested candidates please apply online and complete all screening questions in the online portal.

Last day for applications: Until Filled

Quick apply

Refine Your Search

lead clinical research associate jobs in markham, on

Clinical Research Associate II (SRI) - Odette Cancer Centre Clinical Trials - Regular Full-Time 2026-17987

Clinical Research Associate - Canada

Experienced Clinical Research Associate - Sponsor Dedicated

Clerical Support Associate Prenatal Obstetrical Clinic

Sr. Clinical Operations Lead (Clinical Trial Manager)

Clerical Support Associate Birthing Unit

Therapeutic Area Lead, Specialty Care

Bilingual Sr. Clinical Research Associate

Clerical Support Associate, Fracture Clinic

Clerical Support Associate, Bariatric

Clerical Support Associate, Surgical Prescreening

Clerical Support Associate - OP Mental Health

Clerical Support Associate, Operating Room

Clerical Support Associate, Birthing Unit

Program Implementation Specialist

Clerical Support Associate, Emergency Department, Part time

Clinical Operations & Enablement Lead

Scientific Associate - Pre-clinical Research

Associate Director, Medical Programs

Clerical Support Associate, Post Anesthesia Care Unit (PACU)

I want to receive the latest job alerts for lead clinical research associate in markham, on

Related Searches

Explore jobs in more locations

Job seeker tools

Employer Tools

Browse

Stay Connected