Job Title: Clinical Evaluations Manager
Location: Pennsylvania Avenue, Washington/ Remote
Pay rate: $84/hr.W2
Duration: 12 Months
Shift timings: 9am to 5pm
Description:
This is a role well suited for a self-driven professional looking to expand the impact of Medical Affairs work across the organization.
As a Clinical Evidence Planning and Evaluations Manager, you will be responsible for:
- Creating and driving the Clinical Evidence Strategy for Varian’s devices
- Creation of Clinical Evaluation Plans, Reports, and Post-Market Clinical Evaluation Plans, and Reports (CEP/CER and PMCFP/PMCFR)
- Providing clinical perspective and input to cross-functional teams regarding clinical development, risk management, product management, and post-market surveillance
- Execute Post-Market Clinical Follow Up activities (may include customer surveys, annual literature searches, clinical studies)
- Provide clinical review of promotional material and claims in support of publishing customer facing content
- This position may suit you best if you are familiar with what is below, and would like to develop your skills with Healthineers:
- You have familiarity with design and manufacture medical devices, especially those used in the radiation oncology setting
- You have exemplary technical writing and verbal communication skills
- You prefer an autonomous working environment, as this position is remote.
Required skills and education to have for the success of this role
- Understanding of Clinical Evaluation and Post Market Clinical Follow Up Requirements of class I-III medical devices as designated in the European Union Medical Device Regulation (EU MDR)
- Master’s or PhD in Medical Physics (preferred), Biophysics, Biomedical Engineering. Other degree programs considered based on experience
- 2-5 years’ experience with clinical evaluations, medical physics, or related field.