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$160k – $174k per year
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Confirmed on the employer's own hiring board on Oct 20, 2026. First seen by Alion on Sep 24, 2026.

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Proclinical is a life sciences recruitment and consulting firm headquartered in London that provides executive search, permanent and contract staffing and workforce solutions exclusively to pharmaceutical, biotech, medical device and related companies. Founded in 2005, it runs offices across Europe, North America and Asia-Pacific, including Basel, and places candidates with clients in Switzerland, the UK, the US and Australia. Its current listings are client roles such as scientists, automation and instrumentation engineers, GCP quality managers, project coordinators, finance analysts and veterinary technicians.

Clinical Research Associate - Contract - Orlanda or Tampa, US

Are you ready to lead cutting-edge research projects that accelerate clinical breakthroughs in biotech?

Proclinical is seeking a Clinical Research Associate to support a surgical imaging device study nearing closeout.

Primary Responsibilities:

This role involves a mix of onsite and remote monitoring, with most site visits concentrated in Florida (Orlando and Tampa). Additional studies, including potential pediatric sites in Philadelphia and Jacksonville, are expected to open next year. The focus will be on data cleaning and ensuring the study wraps up successfully by year-end. This is an excellent opportunity for experienced CRAs looking for long-term growth, as the sponsor aims to transition CRAs in-house over time.

Skills &Requirements:

  • Proven experience in clinical monitoring, preferably within medical device studies.
  • Strong understanding of GCP guidelines and regulatory requirements.
  • Ability to work independently and manage multiple priorities effectively.
  • Excellent communication and problem-solving skills.
  • Willingness to travel, primarily within Florida, with occasional trips to other locations.

The Clinical Research Associate's responsibilities will be:

  • Conduct onsite monitoring visits approximately 6-10 days per month, equating to 20-25 hours per week at sites.
  • Oversee study progress, ensuring compliance with protocols, regulatory requirements, and data quality standards.
  • Perform data cleaning and assist in preparing the study for closeout.
  • Collaborate with site staff to address queries and resolve issues promptly.
  • Support the opening of new study sites, including potential pediatric locations.
  • Maintain accurate and timely documentation of monitoring activities.

Compensation:

  • $80 to $87 per hour.

If you are having difficulty in applying or if you have any questions, please contact Alex Kelly at[email protected]

If you are interested in applying to this exciting opportunity, then please click 'Apply' or to speak to one of our specialists please request a call back at the top of this page.

Proclinical is a leading life sciences recruiter focused on finding exceptional people and matching them with the finest positions across the globe. Proclinical is acting as an Employment Agency in relation to this vacancy.

By submitting this application, you confirm that you've read and understood our privacy policy, which informs you how we process and safeguard your data - https://www.proclinical.com/privacy-policy

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