Clinical Research Coordinator (RN/LPN)

The RN/LPN Clinical Research Coordinator will be responsible for performing the day-to-day research and administrative activities of clinical trials, including the implementation, data management, and follow-up to assure data accuracy, patient safety, protocol compliance, and regulatory compliance as required by the clinical trial protocol, the study sponsor, and ICH/GCP standards. This individual will coordinate Phase II-IV trials from initial Sponsor contact for site selection, study preparation and initiation to study completion and close-out.

Requirements for this position include experience including but not limited to:

• Patient Recruitment/Screening/ICF process
• IRB Submissions
• Patient Scheduling
• Following GCP’s
• Prepare Source Documentation and Complete CRF forms in timely manner
• Communicate study needs to principal investigator and other research coordinators
• Sponsor Relations
• Adhering to employee goals and site SOP’s
• Must possess strong computer skills
• Strong background in medical terminology, clinical trials or clinical research required
• Ability to work well independently and in a team environment
• Organized worker that can manage multiple projects
• Excellent written and oral communication skills
• Some travel is required
• Two years of research experience preferred
• RN/LPN required