Clinical Research Coordinator The CLINICAL RESEARCH COORDINATOR plans, implements and coordinates all aspects of study visits according to study protocol; obtains informed consent, takes medical histories from patients, uses assessment skills to detect and report any adverse events to Investigator; manages source documentation and patient's files; serves as focal point for the clinical site for communication with study sponsor, monitor, CRO; attends and participates in investigator meetings. The COORDINATOR also does blood draws, takes vitals signs and performs EKGs and laboratory tasks such as centrifuging and processing blood samples.

Experience with regulatory aspects of clinical research is also essential to this role.

There are both large clinical and administrative components to this position. Studies often require extensive organization and training. The ability to respond to emails in a timely fashion is essential.

The COORDINATOR will also pre-screen potential patients by doing a history, documentation in the patient’s medical chart, and presenting this information the Principal Investigator for review.

QUALIFICATIONS A minimum of 3 years of clinical research experience is mandatory. Registered Nurse diploma, International Medical Graduate Medical Doctor, or Equivalent combination of education & experience.

Certifications: GCP, TCPS-2,



Transportation of Dangerous Goods-Canada, Health Canada Division 5-Drugs in Clinical Trials Involving Human Subjects, Responsible Conduct in Research

Minimum 3 years clinical research, with nursing or medical doctor experience

Phlebotomy, IV starts and ECG skills needed

High proficiency with Microsoft Word, Excel and Outlook

High proficiency with email and Internet navigation

Extreme attention to detail

Solid multi-tasking, organizing and prioritizing The ability to problem-solve and trouble-shoot independently

Exemplary assessment skills mandatory

Fluent in English, French an asset

Excellent communication and interpersonal skills

Ability to effectively organize and prioritize workload

Ability to work independently and as part of a team

Excellent and accurate written documentation skills

No nights, no weekends, but timely responses to emails are required (within one business day)

Only those candidates selected for an interview will be contacted. No phone calls please.

Pay: $30.00-$46.00 per hour

Ability to commute/relocate

- Ottawa, ON K1K 4L2: reliably commute or plan to relocate before starting work (required)

Education:
- Bachelor's Degree (preferred)

Experience:
- clinical research: 3 years (preferred)

Work Location: In person

📌 Senior Clinical Research Coordinator (Ottawa)
🏢 JRB Research
📍 Ottawa