Senior Clinical Research Associate - Orthopedics - Western US region
About The Position
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. ICON is an award-winning workplace that enables you to make a difference to patients’ lives by being part of a world-class clinical research organisation that helps deliver new medicines & medical devices that are benefitting patients worldwide. You are also part of a diverse company that cares about our world and is dedicated to conducting business more sustainably and supporting the communities in which we live. If you’re as driven as we are, join us. You’ll be working in a great environment, with some of the brightest and the friendliest people in the sector, and you’ll be helping shape an industry.
Requirements
- 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.
- 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.
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What This Job Offers
Job Type
Full-time
Career Level
Mid Level
