Remote Associate Medical Director, Oncology

Allucent; Montreal (administrative region); On-site; CAD 140,000 - 200,000; Full time

Benefits offered by this job

Comprehensive benefits

Flexible work hours

Remote or hybrid options

Job summary

Allucent is seeking an Associate Medical Director to join our A-team in a remote capacity. The role focuses on medical monitoring, safety integrity, and protocol-related clinical oversight across oncology trials, with independent work and collaboration with investigators and sites.

Ideal candidates will have MD degree, oncology expertise, and experience in clinical trial safety, data review, and regulatory documentation. This is a full-time, remote opportunity with global study involvement.

Qualifications

• MD degree and oncology expertise required.
• Excellent communication skills in English.
• Experience in clinical trials and safety aspects is preferred.

Responsibilities

• Independently provide medical monitor support to assigned studies, answering medical questions from study team and site; assist with protocol interpretation and medical data review.
• Prepare medical monitoring plans and other relevant study plans before study start.
• Review SAEs, SUSARs, safety narratives and perform analyses of similar events.
• Assist data management with MedDRA coding and WHO terminology.
• Review study documents for medical consistency (CTP, ICF, CSR) and safety reports (DSUR, PSUR).
• Attend and present at Kick-Off and Investigator meetings; provide 24/7 medical support if needed.

Skills

Oncology expertise

Communication skills

English language

Education

MD degree

Tools

Word

Excel

PowerPoint

Job description

Allucent is seeking an Associate Medical Director to join our A-team in a remote capacity. The role focuses on medical monitoring, safety integrity, and protocol-related clinical oversight across oncology trials, with independent work and collaboration with investigators and sites.

Ideal candidates will have MD degree, oncology expertise, and experience in clinical trial safety, data review, and regulatory documentation. This is a full-time, remote opportunity with global study involvement.