Remote Clinical Education Manager, Vascular Trials

Thornton Tomasetti

United States

Remote

USD 99,000 - 199,000

Full time

5 days ago
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Benefits offered by this job

Career development
HIP medical plan
Retirement savings plan
Tuition reimbursement
FreeU education benefit

Job summary

Abbott is seeking a Remote Clinical Education Manager for the Vascular division. You will lead a team within Medical Affairs, focusing on policy, strategy, and oversight of clinical trials, data collection, and final reports.

The role requires 5 years of related experience or a Master’s with 3 years, with strong clinical research and regulatory knowledge. Competitive base salary plus comprehensive benefits.

Qualifications

  • Bachelor's degree or higher in a clinical/scientific field with related experience.
  • Master's degree plus 3 years of relevant work experience is preferred.
  • CRA or direct clinical research experience is desirable.
  • Medical device/diagnostics clinical background is highly preferred.
  • ACRP or SoCRA certifications are a plus.

Responsibilities

  • Oversee strategy implementation and operations for the Medical Affairs Sub-Function.
  • Coordinate clinical trials and reporting; ensure protocol adherence and timely final reports.
  • Recruit clinical investigators and negotiate study design and costs.
  • Direct human clinical trials (Phases III and IV) for products under development.
  • Monitor adverse event reporting and regulatory reporting processes.

Education

Bachelor's degree in a discipline relevant to clinical research
Master's degree with 3 years related experience
Experience as a CRA or direct clinical research
Medical Device/Diagnostics clinical experience
ACRP or SoCRA certifications (preferred)

Job description

Abbott is seeking a Remote Clinical Education Manager for the Vascular division. You will lead a team within Medical Affairs, focusing on policy, strategy, and oversight of clinical trials, data collection, and final reports.

The role requires 5 years of related experience or a Master’s with 3 years, with strong clinical research and regulatory knowledge. Competitive base salary plus comprehensive benefits.

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