Sr Clinical Research Associate

u may be eligible for Medical, Dental, Vision, 401K (no match) and a variety of other benefits to choose from. You may also be eligible for paid time off, including holiday, vacation, and sick/personal time.

Sr. Clinical Research Associate

Desired Locations: Central and West
• To support 4-5 studies in surgical management protocols in the orthopedic medical device space.
• The ideal candidate will have orthopedic medical device monitoring experience.
• 3 years of monitoring experience required.
• 3 years of device 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. Visit Report Metrics: 15 calendar days to submission, 30 calendar days to finalization,
• Travel: 10-12 out of office days per month on average, inclusive of travel.

Posted By: Lea Lolley