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ICON plc

Senior Clinical Research Associate - Orthopedics - Western US region

Reposted 4 Hours Ago
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In-Office or Remote
6 Locations
Senior level
In-Office or Remote
6 Locations
Senior level
The Senior Clinical Research Associate will monitor orthopedic studies, ensuring compliance with FDA regulations, managing risks, and maintaining relationships with stakeholders, while traveling frequently across the Western US.
The summary above was generated by AI

To support 4-5 studies various stages, Orthopedics.  

  • The ideal candidate will have orthopedic medical device monitoring experience- however, other device or pharma monitoring 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 Western US region. Ability to do average 65% travel.

Are you a current ICON Employee? Please click here to apply: link

Top Skills

Clinical Trial Management
Fda Regulations
GCP
Ich

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