Medical Monitor (Canada Board-Certified Gastroenterologist)

Company Description PSI is a leading Contract Research Organization with more than 30 years in the industry, offering a perfect balance between stability and innovation to both clients and employees. We focus on delivering quality and on-time services across a variety of therapeutic indications. Job Description PSI Medical Monitors provide medical input to global clinical studies and advise the teams and business partners, while always focusing on patients' safety and well-being. Home-Based in Canada Responsibilities: Acts as the primary point of contact for all parties on all trial-specific medical and safety-related questions Provides input for responses to regulatory authorities and Institutional Review Boards (IRBs)/Independent Ethics Committees (IECs) on trial-specific medical and safety-related questions Monitors trial participant safety Participates in trial participant recruitment boost and retention activities Presents on medical matters at kick-off and investigator meetings Trains trial team in the therapeutic area and medical aspects of the protocol Develops and reviews trial-specific documents within the scope of medical monitoring Manages ongoing trial risks related to medical monitoring Performs ongoing medical review of the operational clinical trial database; provides support to Medical Reviewer(s) assigned to the trial Reviews protocol deviations Reviews RAE reports, writes and/or reviews SAE narratives, supports Pharmacovigilance team with outstanding safety queries, interacts with sponsor on site safety issues Reviews IND/SUSAR Safety Reports, updates/amendments to essential trial records, and annual IND reports with sponsor data (per sponsor request) Participates in management of trial-related committees (e.g., independent data monitoring committee (IDMC)/adjudication committees) as described in the corresponding trial-specific charter(s) Supports Pharmacovigilance, Medical Data Review and Data Management with reconciliation of safety and operational clinical trial databases Reviews clinical study reports (CSRs), including safety narratives and tables, figures, and listings (TFLs) Provides medical expertise on an as-needed basis in trials where medical monitoring is not a contract deliverable Prepares for and participates in trial audits, follows up on audit findings Participates in feasibility assessment of potential and ongoing trials in the country/region Participates in bid defense meetings and other interactions with clients Acts as a medical expert and provides therapeutic expertise to other PSI departments Qualifications Medical Doctor degree required Canada Board Certification in Gastroenterology required Experience as a practicing Gastroenterology (minimum of 10 years) Clinical Research experience preferred Proficiency with MS Office applications Communication, presentation and analytical skills Problem-solving, team and detail-oriented Additional Information As part of PSI's Medical Monitoring team, you will join our international group of medical professionals, build a career on the frontline of medical science and use your knowledge and expertise to help bring new medications to patients that need them.

The Medical Monitor provides medical expertise and safety oversight for global clinical trials, acting as the primary point of contact for medical and safety-related inquiries. They are responsible for reviewing trial data, managing safety reports, and supporting clinical teams to ensure patient well-being and regulatory compliance.

Candidates must hold a Medical Doctor degree and be a Canada Board-Certified Gastroenterologist with at least 10 years of clinical practice experience. Proficiency in MS Office and strong analytical, communication, and problem-solving skills are required.

• TeamworkPreferred
• Problem solvingPreferred
• CommunicationPreferred

Identified from the job description. Confirm important requirements above.

• Gastroenterology
• Clinical Research
• Medical Monitoring
• Pharmacovigilance
• Regulatory Compliance
• Safety Reporting
• Protocol Development
• Data Management
• Clinical Trial Oversight
• Medical Review
• Communication
• Presentation Skills
• Analytical Skills
• Problem-solving
• Teamwork
• MS Office
• Board Certified/Board Eligible
• Data Monitoring
• Ethical Standards And Conduct
• Research
• Adjudication
• Auditing
• Reconciliation
• Medical Science
• Management
• Clinical Trials
• Clinical Study Reports
• Innovation
• Problem Solving
• Presentations
• Detail Oriented

• Healthcare
• Science & Research
• Consulting
• Gastroenterology Physician/Gastroenterologist
• Physician (Other)
• Specialist Medical Practitioners
• Physicians, All Other

Minimum education

Master’s degree

Minimum experience

10+ years

Posting language

English

Working hours

40 hours per week