Senior Clinical Safety Lead for Medical Device Studies

Avania

California

On-site

USD 42,000 - 70,000

Full time

14 days+

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Benefits offered by this job

Annual bonus
Benefits

Job summary

Avania is seeking a Senior Medical Reviewer to lead safety activities for medical device clinical studies. The role involves translating study protocols into practical safety plans and ensuring participant safety concerns are identified and escalated.

Based in Canada, this position oversees multiple studies across therapeutic areas, coordinating with Medical Reviewers and other functions to maintain progress within client budgets and study timelines.

Qualifications

  • Lead safety activities for medical device clinical studies and translate protocols into safety plans.
  • Coordinate safety activities across studies with operations and client teams.
  • Review clinical information and adverse events; raise questions and escalate safety concerns.
  • Facilitate events committees and coordinate adjudication when required.
  • Mentor junior medical reviewers as you establish in the role.

Responsibilities

  • Translate study protocols into safety management plans and strategy documents.
  • Coordinate safety activities across studies to align with client needs and budgets.
  • Review clinical information and adverse events, identify inconsistencies, and escalate concerns.
  • Facilitate clinical events committees and coordinate member identification and adjudication.
  • Manage competing priorities across studies and therapeutic areas.
  • Mentor junior medical reviewers as you gain experience.

Skills

Safety leadership
Clinical study coordination
Adverse event review
Event adjudication
Mentoring

Job description

Avania is seeking a Senior Medical Reviewer to lead safety activities for medical device clinical studies. The role involves translating study protocols into practical safety plans and ensuring participant safety concerns are identified and escalated.

Based in Canada, this position oversees multiple studies across therapeutic areas, coordinating with Medical Reviewers and other functions to maintain progress within client budgets and study timelines.

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