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Clinical Research Coordinator

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Onsite

Clinical Research Coordinator

Carient Heart & Vascular

Clinical Research Coordinator

Skills

Google Cloud Platform

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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