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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.). Are you a current ICON Employee? Please : link Apply tot his job
