Carient Heart & Vascular
Clinical Research Coordinator
Skills
22 days ago
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Important information
Contract type:
Permanent
Salary:
$54,080 – $66,560 / year
Location:
Manassas, VA, USA
Work mode:
Onsite
Published on:
5 October 2026
What they need
Carient Heart and Vascular is a leading cardiovascular group of 20 cardiologists and 19 mid-level providers in Northern Virginia. We value professional growth, quality colleagues, in a well-established successful group practice; dedicated to providing our patients with the highest level of care. We are looking for a friendly, professional, driven Clinical Research Coordinator to join our patient focused team of professionals at our cardiovascular practice .
Position Summary: The clinical research coordinator is responsible for supporting clinical trials at Carient Heart & Vascular. The Clinical Research Coordinator manages elements of clinical studies in order to meet all protocol obligations while following ICH/GCP guidelines; and company standard operating procedures. The research coordinator is responsible for day-to-day collaboration and coordination between clinical investigators, CRO’s & sponsors to ensure all activities are conducted according to research protocol.
Responsibilities:
· Responsible for Lead study coordinator role on 3-5 Cardiology Clinical Trials
· Screen patient records for identification of prospective candidates for research protocols.
· Educate potential research participants about research protocols and obtains informed consent in accordance with SOP, IRB guidance, and applicable regulatory requirements.
· Generates source documentation and assure accurate collection of data to fulfill protocol design
· Collects, processes and prepares blood and urine specimens for shipping according to protocol requirements
· Completion of Case Report Forms and/or Electronic data capture and respond to queries to meet reporting timelines
Records research activity into RealTime Clinical Trial Management System (CTMS)
· Attends Investigator meetings and educational meetings as necessary
· Adhere to GCP, ICH guidelines when implementing research trials to ensure highest quality research
· Familiarity with SOPs, CLIA as well as other standard research and clinical laboratory practices
Qualifications:
· Bachelor’s degree in Science field
· Phlebotomy Experience
· Cardiology experience a plus
· Good Clinical Practice (GCP) training
· Certified Clinical Research Coordinator (CCRC), Certified Clinical Research Associate(CCRA) or equivalent certification, preferred
**Position may include travel to various Carient office locations
Job Type: Full-time
Pay: $26.00 - $32.00 per hour
Benefits:
- 401(k)
- Dental insurance
- Health insurance
- Paid time off
- Vision insurance
Work Location: In person
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