Sr Clinical Research Associate - Home Based - Midwest/Northeast

To support 1-3 protocols in the cardiovascular/electrophysiology medical device space.

• The ideal candidate will have cardiovascular medical device monitoring experience- however, cardiovascular/electrophysiology pharma monitoring experience will be considered.

5 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 either Midwest or east coast with flexibility to cover potential sites in the northeast (NY/MA), southeast (FL) and midwest (TX, MI, etc.). 

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