Alzheimer’s Disease Clinical Research Coordinator II

Atrium Health Wake Forest Baptist; Winston-Salem (NC); Vor Ort; USD 37.000 - 55.000; Vollzeit

Benefits dieser Stelle

Health benefits

Paid Time Off

Retirement plan with employer match

Educational Assistance Program

Zusammenfassung

Atrium Health Wake Forest Baptist’s Alzheimer’s Disease Research Center seeks a Clinical Studies Coordinator II to coordinate multiple studies of moderate to high complexity. You will oversee recruitment, informed consent, data collection, and regulatory reporting with minimal supervision.

Ideal candidates hold a bachelor’s degree with clinical research experience and familiarity with EPIC/WakeOne and OnCore/WISER systems; SOCRA/ACRP is a plus, with CITI training preferred.

Qualifikationen

• Bachelor's degree with two years' experience in clinical research; or an equivalent combination of experience and education.
• Experience coordinating clinical studies in a research setting is preferred.
• Familiarity with regulatory requirements and patient safety considerations.

Aufgaben

• Coordinates multiple clinical studies with minimal supervision.
• Recruitment activities and informed consent processes.
• Abstracts data and manages case report forms and source documents.
• Maintains regulatory compliance and sponsor reporting requirements.
• Collaborates with interdisciplinary teams and mentors junior staff.

Kenntnisse

Interpersonal communication

Reading comprehension

Organizational skills

Attention to data quality

Regulatory compliance

Team collaboration

Ausbildung

Bachelor's degree with two years' experience in clinical research

Tools

EPIC/WakeOne

OnCore/WISER

Microsoft Office

Jobbeschreibung

Atrium Health Wake Forest Baptist’s Alzheimer’s Disease Research Center seeks a Clinical Studies Coordinator II to coordinate multiple studies of moderate to high complexity. You will oversee recruitment, informed consent, data collection, and regulatory reporting with minimal supervision.

Ideal candidates hold a bachelor’s degree with clinical research experience and familiarity with EPIC/WakeOne and OnCore/WISER systems; SOCRA/ACRP is a plus, with CITI training preferred.