Clinical Research Physician

Translational Research in Oncology; Edmonton; On-site; CAD 110,000 - 140,000; Full time

Job summary

A global clinical research organization is seeking a Clinical Research Physician to join their Medical Monitoring Unit. This full-time, home-based position in Canada focuses on medical monitoring activities for oncology trials, requiring an MD degree and expertise in clinical trials. Ideal candidates have at least one year of experience and strong communication and teamwork skills. Enjoy benefits including vacation, personal time, and flexible working hours.

Benefits

3 weeks vacation

Paid personal/sick time

Paid volunteer day

Flexible working hours

Internet allowance

Home Office Allowance

Employee Family Assistance Program

Qualifications

• 1+ year of medical monitoring experience in oncology trials.
• Current knowledge of ICH GCP guidelines.
• Excellent English proficiency required.

Responsibilities

• Act as Medical Monitor for clinical trials.
• Prepare scientific slides for meetings and trainings.
• Collaborate on trial-specific medical documents.

Skills

Oncology knowledge

Teamwork

Communication skills

MS Office proficiency

Spanish language

Education

Medical Doctor degree

Job description

Translational Research in Oncology (TRIO) is a global clinical research organization dedicated to advancing clinical cancer research. TRIO is looking for a Clinical Research Physician to join our Medical Monitoring Unit team. Reporting to the Medical Monitoring Unit Manager, this will be a home-based, full-time position in Canada.

Main Responsibilities

• Act as Medical Monitor, performing comprehensive medical monitoring activities.
• Respond to medical inquiries from investigational sites and trial teams.
• Review patient eligibility and protocol deviations.
• Oversee patient safety by reviewing medical data at patient and trial levels.
• Review Serious Adverse Events (SAEs), including coding, causality and expectedness assessments, and drafting company comments.
• Prepare scientific slides, attend and/or present protocol information at Investigator Meetings, Scientific Committee meetings, Safety Review Committee meetings, SIVs, etc.
• Serve as the primary clinical point of contact for scientific questions from internal and external stakeholders (e.g., IRBs, sites, sponsor medical teams, trial teams).
• Collaborate with the Medical Writing and Training Unit to write and/or review trial‑specific medical documents (e.g., protocols, DSURs, CSRs).
• Conduct medical training on selected trial‑specific or non‑trial‑specific topics.

Qualifications

• Medical Doctor degree required.
• Excellent knowledge and understanding of oncology and oncology clinical trials.
• At least 1 year of experience in medical monitoring in oncology trials.
• Current knowledge of ICH GCP guidelines.
• Advanced proficiency in MS Office in Word, Excel, and PowerPoint.
• Strong teamwork abilities and communication skills.
• Excellent level of English is required.
• Spanish language knowledge will be valued.
• Must be legally authorized to work in the country.

What TRIO Can Offer You

• 3 weeks of vacation plus paid December Holiday Closure.
• 10 days paid personal/sick time.
• 1 paid volunteer day per year.
• Flexible working hours to promote work‑life balance.
• Monthly Internet allowance to support working from home and a one‑time Home Office Allowance.
• Employee Family Assistance Program to support you and your family during difficult times.

Pay Range $110,000.00 to $140,000.00 annually – Salary influenced by education, experience, location, knowledge, skills, abilities of the applicant, internal equity, and alignment with market data.

Prior to applying please review TRIO's Applicant Information Notice.

Teamwork · Passion · Integrity · Innovation