Clinical Research Coordinator II: Study Operations & Compliance

Prisma Health; Greenville (SC); On-site; USD 55,000 - 75,000; Full time

Job summary

Prisma Health in Greenville, SC seeks a Clinical Research Coordinator to manage day-to-day clinical trial activities at Cancer Centers - Faris Road, ensuring data integrity and protocol adherence.

Education and experience requirements are a Bachelor's in Health Sciences or related field and 2 years of research; duties include coordinating visits, data collection, and regulatory submissions.

Qualifications

• Bachelor's Degree in Health Sciences or Business-related field.
• Minimum 2 years of research experience in pharmaceutical, academic, device, NIH, investigator-initiated studies or registry trials.
• In lieu of education and experience, an equivalent combination of work experience and academic experience may be considered.

Responsibilities

• Coordinate day-to-day study operations and contribute to program growth.
• Monitor protocol compliance and oversee data collection tools.
• Manage participant visits and protocol-required procedures.
• Communicate study progress to investigators and regulators.
• Assist sponsor- and investigator-initiated trials per protocols.

Skills

GCP principles

Regulatory knowledge

Data abstraction

Study coordination

Communication

Education

Bachelor's Degree in Health Sciences or Business-related field

Job description

Prisma Health in Greenville, SC seeks a Clinical Research Coordinator to manage day-to-day clinical trial activities at Cancer Centers - Faris Road, ensuring data integrity and protocol adherence.

Education and experience requirements are a Bachelor's in Health Sciences or related field and 2 years of research; duties include coordinating visits, data collection, and regulatory submissions.