Posted 4 days ago
Clinical Research Associate
@ adecco
Ottawa, Ontario
Overview
Adecco is hiring a full-time contract Clinical Research Associate for a medical device and healthcare technology organization in Ottawa, ON, at $80,000-85,000 per year. The role coordinates clinical studies, maintains trial documentation in Veeva's Trial Master File, conducts monitoring visits and supports site activities, with travel to clinical sites as required. Weekday schedule, Monday to Friday.
Pay:
$80,000–$85,000 a year
Responsibilities:
- Coordinate and support clinical studies per protocols
- Manage TMF documentation in Veeva
- Conduct monitoring visits and site follow-ups
- Assist with clinical documents, protocols and CRFs
- Work with internal teams and clinical sites
Requirements summary:
- 2+ years conducting clinical studies
- Knowledge of clinical research regulations
- Science degree preferred
- Experience with medical devices or diagnostics an asset
- Veeva and TMF experience an asset
- Legally eligible to work and reside in Canada
Tools & skills
Benefits mentioned
Source and dates
Employer career site / ATS feed · careerpage
- Employer posting date
- 2026-11-02
- First seen by our source
- 2026-10-10
- Source record updated
- 2026-11-02
These dates describe the source record, not a live verification that the employer is still hiring. Check the original posting.
Job details
| Seniority | Mid level |
| Department | Allied health |
| Experience | 2+ years |
| Hours per week | 40 |
| Schedule | day |
| Travel | ground: moderate |
| Work setting | Office, Client sites |
| Position | Sitting and standing |
| Physical demands | physical low · computer high |
| Languages | English |
| Education | Bachelor’s degree (preferred) |
| Fields of study | Science |
| Perks mentioned | Paid training |
Summary and details written by AI from the posting; the employer’s posting is the authority.
adecco
| Field | Value |
|---|---|
| Headquarters | Düsseldorf |
| Open jobs on Jobsy | 638 |
Adecco is currently hiring a full-time Clinical Research Associate for an opportunity with a leading medical device and healthcare technology organization in Ottawa, ON. This role is ideal for candidates with experience in clinical research, clinical studies, medical devices, diagnostics, laboratory operations, regulatory compliance, and clinical trial support.
Pay Rate: $80000-85000/year
Location: Ottawa, ON
Shift: Monday to Friday
Job type: Temporary | Full-time
Vacancy Status: This posting is for an existing vacancy.
Here's why you should apply:
Paid weekly accurate and on time
Strong health and safety programs
Medical and dental benefits once qualified
Free training programs
New and quicker onboarding process
Responsibilities:
Clinical Study Coordination
Coordinate and support clinical studies in accordance with protocols and regulatory requirements.
Collect, maintain, and manage study documentation.
Manage Trial Master File (TMF) documentation using Veeva.
Conduct monitoring visits, site follow-ups, and visit reporting.
Support workflow testing, study preparation, and site activities.
Clinical Documentation & Compliance
Assist with the preparation of clinical documents, protocols, CRFs, and reports.
Review and document study results.
Support the development and maintenance of study procedures.
Ensure compliance with quality and regulatory standards.
Collaboration & Site Support
Work closely with internal teams and clinical sites.
Communicate effectively with study stakeholders.
Travel to clinical sites as required to support study activities.
Qualifications and Skills:
Bachelor's degree in Science or a related field preferred.
Minimum 2 years of experience conducting clinical studies.
Knowledge of clinical research regulations and quality standards.
Clinical laboratory, medical device, diagnostics, or sample handling experience is an asset.
Strong organizational and documentation skills.
Excellent communication and interpersonal abilities.
Ability to manage multiple priorities in a fast-paced environment.
Self-motivated with strong attention to detail and problem-solving skills.
Willingness to travel to study sites as required.
Experience with Trial Master File (TMF) management and Veeva is considered an asset.
Must be legally eligible to work, and reside in Canada
Are you interested in this position? Apply now! Our dynamic team of recruiters will reach out if you qualify for this role.
At Adecco our purpose is simple: to make the future work for everyone. We live our values, Passion, Collaboration, Inclusion, Courage, and Customers at Heart, by fostering a workplace where diversity is celebrated and every voice matters. We encourage applications from individuals of all backgrounds and identities. Together, we’re making the future work for everyone.
Please reach out to learn how the Aspire Academy can upskill you into your next role.
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