Senior Clinical Research Associate - Cardiovascular Device - Central/West Region
To support 1study in the cardiovascular/electrophysiology medical device space. Indication is A-fib.
- The ideal candidate will have cardiovascular medical device monitoring experience- however, complex experience in cardiovascular/electrophysiology pharma monitoring and/or Coordinator/Nursing experience will be considered.
3 years of monitoring experience required.
A bachelor's degree is required, preferably a Bachelor of Science Degree in Life Science, Physical Science, Nursing or Biological Science.
Candidates must have/ be:
- 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.
- A well-executed plan for communication with the study teams and sites.
- Well-versed in clinical trial management. They are rigorous, detail-oriented, and precise in their reports.
- Located in the West region in the US near a major airport. Ability to cover up to 65% regional travel.
