Clinical Research Physician at Translational Research in Oncology TRIO

Vancouver, British Columbia, Canada -

Full Time

Start Date

Immediate

Expiry Date

19 Jun, 26

Salary

140000.0

Posted On

21 Mar, 26

Experience

0 year(s) or above

Remote Job

Yes

Telecommute

Yes

Sponsor Visa

Skills

Medical Monitoring, Oncology, Clinical Trials, Medical Inquiries, Patient Eligibility Review, Protocol Deviations Review, Patient Safety Oversight, Serious Adverse Events Review, Scientific Slide Preparation, Scientific Communication, Clinical Point of Contact, Medical Writing Collaboration, Medical Training, Teamwork, Communication Skills, MS Office Proficiency

Industry

Research Services

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. Prepares scientific slides, attends and/or presents 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). Collaborates with the Medical Writing and Training Unit to write and/or review trial-specific medical documents (e.g., protocols, DSURs, CSRs). Conducting 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 / 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 Monthly Internet Allowance to support working from home and a one-time Home Office Allowance Pay Range $110,000.00 to $140,000.00 annually - Salary to be influenced (or determined) by the 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 To support efficiency, TRIO may use limited AI tools during the candidate review process. All hiring decisions are made by people, not AI. To ensure fairness and an accurate understanding of your skills, we ask that candidates refrain from using AI tools or AI‑generated responses during interviews or assessments. We want the opportunity to get to know you and your experience. Teamwork · Passion · Integrity · Innovation

Responsibilities

The Clinical Research Physician will act as the Medical Monitor, performing comprehensive medical monitoring activities such as responding to site inquiries, reviewing patient eligibility, and overseeing patient safety by analyzing medical data. This role also involves preparing scientific materials and serving as the primary clinical contact for scientific questions from various stakeholders.