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- Conducts activities required to create, update, and manage clinical evaluation plans, reports, and post market clinical follow up plans and reports.
- Responsible for supporting clinical evaluation and post market clinical follow up deliverables through the following activities:
- Complaint/public Adverse Events analysis.
- Literature searches and appraisals.
- Cross functional input for Post Market Surveillance and Risk Management teams
- Post Market Clinical Follow Up surveys.
- Support clinical review of material submitted to promotional review and medical affairs review committees.
- Opportunities to cross-functionally to ensure clinical evaluations are integrated with business needs on clinical evidence strategy to facilitate career growth.
- Minimal requirements:
- Bachelor's degree in physical or life science or relevant experience (3 to 5 years in a position with R&D in life science and technical writing)
- Strong verbal and written skills.
- Ability to explain, influence and advocate (both in writing and in person) to advance Varian's goals.
- Strong project management and organizational skills.
- Strong interpersonal and teamwork skills.
- Research, medical, or technical background
- Preferred Skills & Experience:
- Masters in an oncology related field with strong publication and technical writing background.
- Experience with:
- Radiation therapy and oncology.
- Medical device industry.
- Clinical Evaluation Reports (EU MDR).
- Experience working with global team.
Clinical Evaluations Specialist - Washington, United States - Hired by Matrix
Description
Job Description
Job DescriptionWhat You'll Do:
What You'll Bring: