Clinical Research Coordinator II – HIV & Substance-Use Trials

Advocate Health; Winston-Salem (NC); On-site; USD 52,000 - 70,000; Full time

Job summary

Wake Forest Baptist Health is seeking a Study Coordinator to support NIH-funded clinical research on HIV-related outcomes in North Carolina. Responsibilities include participant recruitment, enrollment, data collection, and coordination of multimodal assessments such as interviews, neuropsychology testing, and lab work.

The role involves regulatory duties, data management, and collaboration with investigators.

Qualifications

• Bachelor's degree with two years of clinical research experience or equivalent.
• SOCRA or ACRP certification preferred; CITI certification required.
• WakeOne training required for research coordinators.

Responsibilities

• Recruitment and enrollment of study participants.
• Coordinate visits and data collection according to protocol.
• Abstract data from medical records and complete case report forms.
• Ensure data quality and regulatory compliance.
• Liaise with investigators and supervise auxiliary staff.
• Maintain source documents and report adverse events as required.

Skills

Interpersonal communication

Oral communication

Written communication

Reading comprehension

Organizational skills

EPIC/WakeOne proficiency

OnCore/WISER TM

Computer skills

Confidentiality

Microsoft Office

Education

Bachelor's degree with 2+ years clinical research

Tools

EPIC/WakeOne

OnCore/WISER

Job description

Wake Forest Baptist Health is seeking a Study Coordinator to support NIH-funded clinical research on HIV-related outcomes in North Carolina. Responsibilities include participant recruitment, enrollment, data collection, and coordination of multimodal assessments such as interviews, neuropsychology testing, and lab work.

The role involves regulatory duties, data management, and collaboration with investigators.