Senior Clinical and Medical Affairs Strategist

12 hours ago


Canada Brunel Full time

Company Overview:

Brunel is a leading recruitment agency with a global network of clients and talented individuals. With over 45 years of experience, we pride ourselves on working with some of the best in the business.

About the Role:

We are seeking an experienced Clinical and Medical Affairs Manager to join our team. The successful candidate will be responsible for ensuring compliance with regulations, managing clinical trials, and evaluating investigational sites in North America.

Key Responsibilities:

  • Ensure full compliance with all appropriate regulations: SOPs, GCPs, FDA, and Health Canada regulations.
  • Assist in the planning, management, and execution of clinical trials.
  • Help identify and evaluate investigational sites in North America.
  • In collaboration with external vendors, assist in building, organizing, and maintaining the Trial Master File throughout the study.
  • Collaborate with vendors for Medical Writing, Medical Monitoring, Data Management, and Statistics, as required.
  • Help with planning and management of study budgets.
  • Secure IRB study approvals and help with sites' IRB submissions and approvals.
  • Support business development efforts by building and maintaining relationships with industry professionals, clinicians, and investigators.
  • Collaborate and support North American medical affairs activities, such as training sessions, advisory boards, CME events, presentations, etc.

What We Offer:

We offer a competitive salary range of $85,000 - $115,000 per year, depending on experience. In addition, we provide a comprehensive benefits package, including health insurance, retirement savings plan, and paid time off.

Requirements:

  • University degree or Masters (scientific).
  • Minimum 3-5 years of experience in clinical and medical affairs management in the pharmaceutical or medical device industry.
  • Excellent written and oral communication skills.
  • Bilingual (English and French) would be preferred.
  • Track record of completed clinical trials, from conception to publication (drugs and/or medical devices).
  • Experience in medical affairs activities, such as advisory boards, IITs (Investigator-Initiated Trials), educational programs development, etc.

About Us:

Brunel has a reputation for working with some of the best in the business. That's what we continually strive for. Over 45 years, we've created a global network of interesting clients and talented individuals working together through a vast array of services.



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