Sr Clinical Research Associate (Cardio Medical Device) - Home Based - Midwest/Northeast
This a Full Remote job, the offer is available from: New York (USA), Texas (USA)
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 click here to apply: link
This offer from "ICON plc" has been enriched by Jobgether.com and got a 83% flex score.
Apply Now
Apply Now
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 click here to apply: link
This offer from "ICON plc" has been enriched by Jobgether.com and got a 83% flex score.
Apply Now
Apply Now