Grant-Funded Clinical Research Coordinator II

Advocate Health; Winston-Salem (NC); On-site; USD 60,000 - 82,000; Full time

Job summary

Wake Forest Baptist Health seeks a Clinical Studies Coordinator II - Translational Neuroscience to advance neuroscience research by coordinating studies, supporting recruitment and visits, and ensuring regulatory compliance. You will collaborate with investigators to translate discoveries into improved patient care, requiring strong organization and attention to detail.

The role involves data abstraction, source documentation, and adherence to Wake Forest policies, with opportunities to mentor

Qualifications

• Bachelor's degree in a related field or equivalent clinical research experience.
• Experience in clinical research or coordinating studies is required.
• SOCRA or ACRP certification preferred; CITI training required if not completed.

Responsibilities

• Coordinate clinical research studies under supervision of investigators or manager.
• Play an active role in recruiting patients to studies and assist with visits.
• Perform protocol-specific duties as required by the research protocol.
• Obtain or assist with informed consent and reinforce study information.
• Fulfill sponsor reporting requirements including adverse events and data events.
• Abstract data from medical records and complete paper/electronic CRFs accurately.
• Identify protocol/data issues and communicate them to the supervisor promptly.
• Provide staff relief as needed; attend team meetings and quality projects.

Skills

Interpersonal skills

Oral communication

Written communication

Reading comprehension

Organizational skills

EPIC/WakeOne

OnCore/WISER

Clinical trial data management

MS Office

Data documentation

Confidentiality

Education

Bachelor's degree with two years experience in clinical research

Tools

EPIC/WakeOne

OnCore/WISER

Microsoft Office

Job description

Wake Forest Baptist Health seeks a Clinical Studies Coordinator II - Translational Neuroscience to advance neuroscience research by coordinating studies, supporting recruitment and visits, and ensuring regulatory compliance. You will collaborate with investigators to translate discoveries into improved patient care, requiring strong organization and attention to detail.

The role involves data abstraction, source documentation, and adherence to Wake Forest policies, with opportunities to mentor