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Sr. Clinical Research Associate
Job in
New Brunswick, Middlesex County, New Jersey, 08933, USA
Listed on 2026-01-12
Listing for:
Vita Global Sciences, a Kelly Company
Full Time
position Listed on 2026-01-12
Job specializations:
-
Healthcare
Clinical Research, Medical Science
Job Description & How to Apply Below
Join to apply for the Sr. Clinical Research Associate role at Vita Global Sciences, a Kelly Company
.
Kelly Science and Clinical FSP is currently seeking a Regional Clinical Research Associate for a long‑term engagement in the U.S. with one of our Global Medical Device clients. This full‑time role offers full benefit options. As a Kelly FSP employee you may be eligible for Medical, Dental, Vision, 401(k), and a variety of other benefits, as well as paid time off including holiday, vacation, and sick/personal time.
RegionalClinical Research Associate
Regional travel flexing up to 75%.
Responsibilities and Qualifications- Support 1‑3 protocols in the cardiovascular/electrophysiology medical device space.
- Ideal candidate will have cardiovascular medical device monitoring experience; however, cardiovascular/electrophysiology pharma monitoring experience will also be considered.
- Minimum 5 years of monitoring experience.
- Bachelor’s degree required, preferably a Bachelor of Science in Life Science, Physical Science, Nursing or Biological Science.
- In‑depth knowledge of FDA regulations and ICH/GCP guidelines.
- Strong problem‑solving skills to mitigate risks and identify issues at sites and implement effective solutions promptly.
- Strong interpersonal skills to establish and maintain effective working relationships with site personnel, investigators, and internal teams.
- Exceptional verbal and written communication skills, with the ability to convey complex information clearly and concisely.
- Ability to tailor communication style to the needs and preferences of different stakeholders, fostering a collaborative environment.
- Ability to work independently and manage multiple priorities in a dynamic environment.
- Well‑executed plan for communication with the study teams and sites.
- Well‑versed in clinical trial management; rigorous, detail‑oriented, and precise in their reports.
Position Requirements
10+ Years
work experience
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