Regulatory Affairs Expert

2 weeks ago

Old Toronto, Canada Lock Search Group Full time
Job Description

Lock Search Group is seeking a driven and experienced Regulatory Affairs Expert to lead its Medical Affairs team as a Senior Manager. This full-time position reports directly to the Director of Medical Affairs.

About the Role

This leadership position plays a pivotal role in advancing scientific education, support for healthcare professionals, patient advocates, and community organizations within a specific therapeutic area. As a key member of our Medical Affairs team, you will design and implement comprehensive medical plans focused on community engagement for treatment and prevention strategies.

Responsibilities
  • Develop and oversee educational programs tailored to community audiences addressing critical topics in healthcare with scientific accuracy.
  • Collaborate with cross-functional teams to ensure alignment of community engagement initiatives with broader medical strategies and organizational objectives.
  • Create accessible tools and resources supporting community stakeholders in understanding treatment and prevention options.
  • Lead advisory boards and community-focused discussions to gather insights informing medical strategies.
  • Identify and support community-driven research initiatives fostering collaborations aligned with the organization's scientific goals.
  • Serve as a liaison between internal departments ensuring educational and community initiatives align with other functional areas.
  • Represent the organization's medical expertise through balanced, science-driven presentations at community events, workshops, and forums.
  • Ensure compliance with regulatory requirements including proper reporting of adverse events and adherence to pharmacovigilance protocols.
Requirements
  • Advanced degree in a relevant field (Masters or higher).
  • A strong medical, clinical, or scientific background is required.
  • At least 2 years of industry experience in Medical Affairs is preferred.
  • Exceptional project management and organizational skills.
  • Strong written, verbal, and interpersonal communication abilities with experience building relationships and negotiating.
  • Skilled at utilizing scientific resources to develop educational content and presentations for various audiences.
  • Able to manage multiple projects simultaneously while prioritizing workload effectively.
  • Thorough understanding of regulatory and legal requirements related to clinical trials and Medical Affairs activities.
What We Offer

We offer a competitive salary range of $120,000 - $180,000 per annum, depending on experience, along with a comprehensive benefits package and opportunities for career growth and professional development.

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