No more applications are being accepted for this job
- As part of the clinical evaluations team at Varian, this person 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
- 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
- DESIRABLE (Not essential, but highly advantageous)Masters in an oncology related field with strong publication and technical writing background.
- Experience with radiation therapy and/or oncology.
- Experience within medical device industry
- Experience writing Clinical Evaluation Reports (EU MDR)
- Experience working with global team
- Interest in career advancement
Clinical Project Manager - Washington, United States - Net2Source Inc.
Description
Job Title: Commercial Project Manager 1
Duration: 12 months (Possible Extension)
Location: Washington, DC USA 20004
Pay Rate: $45/hour on w2
9 AM - 5PM
Description:
Clinical Evaluations Specialist
Skills, Experience and Qualifications