Clinical Research Coordinator

Pharmaceutical CLINICAL RESEARCH COORDINATOR POSITION and ASSISTANT COORDINATOR POSITION in Women's Health OB-GYN Division- Successful candidates for the full time position will have clinical research coordination experience, be science-minded, friendly, highly motivated, and detail oriented. Candidates must be comfortable working in a fast paced medical office environment, be highly organized, and know how to prioritize effectively. Candidates must utilize in-depth knowledge of protocol requirements to ensure that studies are properly conducted in conformance with the protocol guidelines, and good clinical practices as set forth by federal regulations. Must exhibit sound conduct of the clinical trial including recruitment, screening, enrollment and follow-up of eligible subjects according to protocol requirements. Must have strong interpersonal skills as the position involves interaction with patients (both over the phone and in person), physicians and midlevel providers as well as other coordinators in a team-like environment. Candidates must communicate effectively in English (oral and written.) Candidates must have at least a bachelor's degree (BA/BS,) preferable in the Health Sciences /Sciences, but experience in lieu of degree will be considered.Candidates will have experience in the following:Coordinating multiple clinical research studies simultaneously while adhering to the principles of Good Clinical PracticePerforming informed consent, screening, enrolling, scheduling and coordinating appointments, conducting research visits, recording medical histories, collecting and entering data into Source and CRFs from patients and other appropriate sourcesWorking as a cohesive team member coordinating assigned studies and backing up other studiesEducating and providing information to patients, families, and community groups regarding clinical drug trialsAssisting and supporting Recruitment Team with prescreening activities and other activities related to subject recruitmentAttending Study related training and site initiation meetingsPerforming Inventory control, handling, and maintaining accountability for all study supplies and investigational productsFacilitating study monitoring visits and prompt resolution of all study related queriesMaintaining accurate and complete documentation of related regulatory documents.Maintaining professional and appropriate interactions with sponsors and all other study related personnel, subjects, families, and staff members.Understanding of medical terminology (basic-intermediate)Proficiency with MS Office (Word, Excel), email, internet, data entry.Other duties as assignedPositive candidate must possess the following:Commitment to excellence and quality patient careHigh organizational ability with strong attention to detail and accuracyCritical thinking and problem solvingIntermediate computer skillsFull time position, Salary commensurate with experience and qualifications, healthcare benefits, and 401(k) with company match. The primary work location for this position will near Sentara Leigh Hospital.Time Frame: Immediate OpeningJob Type: Full-time. Please note, this is not a bench/laboratory research position.