Clinical Research Coordinator

Proclinical is currently seeking an experienced Clinical Research Coordinator for a gastroenterology practice. This group of professionals are a mid-size practice who cares about the employees. This will be a great role for someone with excellent clinical trial experience. The Clinical Research Coordinator is responsible for following federal and sponsor guidelines, coordinating, performing and overseeing clinical trials data management, scheduling trial treatments and following up on care of clinical trials. Successful candidate must have basic clinical competence: taking of vital signs and phlebotomy skills.

Job Responsibilities

• Prepare new and renew protocols as well as ongoing amendments, modifications and revisions.
• Support the safety of clinical research participants.
• Educate subjects and family on protocol, study intervention, study drug, etc.
• Facilitate pre-study, site qualification, study initiation, monitoring visits and close out activities.
• Maintain study source documents and regulatory documents.
• Understand good clinical practice and report adverse events.

Skills and Requirements

• Must be experience in taking vital signs and have phlebotomy skills
• At least 3 years of clinical trials background
• ACRP or SOCRA membership preferred

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 Anula Aboobacker at (+1) 646-367-2909 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.

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