Clinical Research Physician

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

3 weeks of vacation plus paid December Holiday Closure

$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.

Act as Medical Monitor, performing comprehensive medical monitoring activities.

Respond to medical inquiries from investigational sites and trial teams.

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).