In-House Clinical Research Associate

At Proclinical, we are seeking an individual to fill the role of In-House Clinical Research Associate, based in Jacksonville, FL.

Responsibilities

• Work to ensure that trials are adhere to applicable internal and external standards, guidelines and requirements.
• Evaluate, monitor, and document study results.
• Monitor Clinical Research Organizations (CROs) and study management of multiple sites.
• Manage designated clinical trials.
• Ensure procedures are in place for appropriate optimization of patients into the clinical trial.
• Plan requirements for clinical trial material (CTM), ordering CTM, setting up and monitoring the systems whereby the CRA can ship CTM to the investigator, maintaining procedures to account for the CTM, checking the expiration of CTM, and requesting extensions if necessary.
• Approximately 15% local on-site monitoring.

Skills And Qualifications

• BA in related and 1-3 years of experience in medical device research and/or in-house CRA.
• Electronic Data Capture (EDC) experience required (non-discriminatory)
• On-site monitoring experience is preferred.
• Excellent written, verbal, and interpersonal communication skills.
• Domestic travel up to 15%.

To Apply:

Please click on the Apply button. Please include a short note outlining why you are interested in the role and why you think you are suitable.

In case you have difficulty in applying or if you have any questions, please call Mary Jacobs at (+1) 2674774800 or upload your resume on our website - www.Proclinical.com.

A full job description is available on request.

Proclinical is a specialist employment agency and recruitment business, providing job opportunities within major pharmaceutical, biopharmaceutical, biotechnology and medical device companies.