Clinical Research Coordinator (CRC), Level 1 Wage – NICU, Department of Pediatrics (Staff Wage)

University of Virginia

1d•Onsite

About The Position

The Department of Pediatrics in the University of Virginia’s (UVA) School of Medicine is seeking an applicant for a Clinical Research Coordinator (CRC), Level 1 (wage) to join the NICU/PICU CRC team in supporting Neonatal Intensive Care Unit (NICU) research. This CRC-1 will play a key role in supporting multiple ongoing clinical research studies with a particular emphasis on subject recruitment for active studies which include sponsored drug/device trials, NIH funded research, and investigator-initiated trials. This role involves intense cumulative learning of NICU workflow and offers an opportunity to contribute meaningfully to impact neonatal research by gaining hands-on experience in a collaborative and supportive clinical research environment. This position will be integrated into the NICU/PICU Clinical Research Coordinator team. The team will provide structured onboarding, training, and ongoing support to ensure a successful transition into the role and development of subject recruitment skills specific to the NICU environment.

Requirements

Bachelor's Degree or equivalent combination of experience, education and or certifications required.
None. Some experience in a healthcare setting and/or knowledge of medical terminology is preferred.
None.

Nice To Haves

Bachelor’s degree, preferably in a scientific, public health, or related discipline.
An advanced degree in scientific or health related field preferred but not required.
Strong organizational skills and attention to detail
Excellent communication and interpersonal skills
Ability to work independently and as part of a collaborative team
Flexibility to accommodate on-call responsibilities
The ideal candidate will be a motivated and detail-oriented learner with a strong work ethic who will demonstrate respect for all persons with high moral character, recognizing the sensitivity and ethical responsibility inherent in the NICU environment.

Responsibilities

Support day-to-day operations of multiple concurrent clinical trials in the NICU.
Assist with subject recruitment efforts, including screening, consent coordination, and enrollment for trials.
Maintain accurate and timely study documentation in compliance with regulatory and institutional requirements.
Coordinate with investigators, NICU clinical staff, and NICU/PICU CRC team to ensure protocol adherence.
Assist with data collection and entry.
Assist with specimen collection, processing and shipping.
Communicate effectively with study sponsors and internal stakeholders as needed.