Medical Monitor

Job Description

ClinChoice is seeking a Medical Monitor to join their team. This is a hybrid position based in either Quebec, Canada, or Pennsylvania, US. The Medical Monitor will provide clinical support to the Clinical Operations team throughout the clinical trial lifecycle, from study design to result dissemination.Responsibilities:

• Serve as the Clinical Advisor, answering medical questions throughout the clinical trial.
• Participate in project meetings, providing medical advice.
• Review study data listings from a medical perspective.
• Analyze and interpret study data/results independently.
• Write and review protocols, Case Report Forms (CRF), and Clinical Study Reports (CSR).
• Provide training in specific disease/therapeutic areas.
• Assist in developing criteria for investigator site selection and networking.
• Participate in subject recruitment and retention activities.
• Present protocol and safety reporting information at Investigator Meetings.
• Provide on-call coverage for medical queries related to the protocol.

Requirements:

• University Degree in medical disciplines.
• At least two (2) years of medical experience.
• Previous experience or knowledge of the clinical trial process.
• Fluent in English and local language(s).
• Proficiency in Microsoft Office (e.g., Word, Excel, Outlook).
• Willingness to travel.

Benefits:

• Opportunity to make a difference in peoples’ lives.
• Fulfilling and rewarding career.
• Excellent work-life balance.
• Collaborative “one-team” culture.