Newark, United States
about 1 year ago
Candidate will support Clinical Affairs IVDR efforts, including writing and reviewing clinical and scientific reports, performing literature searches, and summarizing the results of literature searches performed in clinical databases.
- Bachelor's degree in a scientific field with a minimum of 5-10 years' experience; preferably with some clinical writing, reviewing, or regulatory experience.
- Strong technical background, preferable in the diagnostics or medical device industry.
- Strong interpersonal, communication, and organization skills; ability to communicate issues in a timely manner and develop mitigations.
- Ability to set and manage priorities independently and adapt to changing priorities.