- 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.
- ESSENTIAL (minimal requirements for interview).
- Bachelor s degree in physical or life science or relevant experience (3-5 years in a position with R&D in life science and technical writing).
- Strong verbal and written skills.
- Strong 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.
- Masters in an oncology-related field with a strong publication and technical writing background.
- Experience with radiation therapy and oncology.
- Experience within the medical device industry.
- Experience writing Clinical Evaluation Reports (EU MDR).
- Experience working with a global team.
- Interest in career advancement.
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