Clinical Research Coordinator

Have you been looking for a place to grow your skillset? Or perhaps you are looking for a place to develop your career surrounded by a diverse group where employees feel a sense of belonging.

At Colon, Stomach, Liver Center, we are championing the power of inclusivity and a people first mentality. We hope to improve the human experience – from our patients to our colleagues.

If you are interested in joining our culture, we’re looking for a full-time Clinical Research Coordinator in our Research Center located at 19455 Deerfield Ave, Lansdowne, VA.

What's in it for you?

• 401k with match
• Tuition reimbursement
• The best swag with the coolest logo…OG
• Excellent paid time off for balance of work/life
• Internal growth opportunities with training and development
• Competitive health & supplemental benefits
• Impact somebody’s life and make a difference

Snapshot of Daily Duties:

• Administratively and clinically manage industry sponsored clinical trials.
• Assist in patient recruitment by performing detailed chart reviews and patient interviews.
• Discuss study protocols with patients and verify the informed consent documentation.
• Review medical history of patient against inclusion/exclusion criteria of studies.
• Perform blood draws, process and ship blood/urine specimens per study protocol and IATA regulations.
• Schedule all patient research visits and procedures consistent with protocol requirements.
• Dispense study medication, collect vital signs, and perform ECGs.
• Complete and maintain case report forms per FDA guidelines and review them against the patient’s medical record for completeness and accuracy.
• Maintain compliance of protocols and regulatory guidelines for studies performed in the research area.
• Perform phlebotomy for lab work as required and completes all necessary forms.
• Monitor the progress of research activities; develop and maintain records of research activities, and prepare periodic and ad hoc reports, as required by investigators, administrators, funding agencies, and/or regulatory bodies.
• Triage phone calls from subjects, be able to answer clinical care questions within the scope of practice; determine when escalation is required.

Must Haves:

• High School Diploma or equivalent required.
• Associates degree in a clinical or scientific related discipline required. Bachelor's degree is preferred.
• One (1) year previous experience as a clinical research coordinator for pharmaceutical phase II or III trials required.
• Must maintain current licensure and/or certification.
• BLS certified.
• Knowledge of medical terminology, anatomy, physiology, and pathophysiology.
• Understanding of clinical research documentation standards.
• Understanding of Code of Federal Regulations for Human Subjects.
• Certified in GCP’s and HSP.
• Periodic local travel to other practice locations on an as-needed basis.
• Phlebotomy experience preferred.