Sr Clinical Research Associate - Home Based - Midwest/Northeast
About The Position
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.).
Requirements
- 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
- 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.)
Stand Out From the Crowd
Upload your resume and get instant feedback on how well it matches this job.
What This Job Offers
Job Type
Full-time
Career Level
Mid Level
Number of Employees
5,001-10,000 employees
