Clinical Trials Operations Specialist

Prisma Health; Greenville (SC); On-site; USD 60,000 - 85,000; Full time

Job summary

Prisma Health’s Upstate Administrative Research Staff in Greenville seeks a Clinical Research Coordinator to manage and oversee clinical trial studies, educate staff, and ensure data integrity and compliance across trials.

Responsibilities include coordinating patient visits, data collection, regulatory submissions, and communications with investigators and regulatory bodies; you’ll work with the health care team to ensure protocol adherence.

Qualifications

• Bachelor's degree in Health Sciences or related field as minimum.
• 2+ years of research experience in pharmaceutical, academic, device, NIH, investigator-initiated studies or registry trials.
• BLS within six months of employment; CITI preferred.

Responsibilities

• Oversee implementation and management of clinical trial studies.
• Educate research staff, healthcare team and participants/caregivers.
• Coordinate data collection tools, regulatory submissions, and study communications.

Skills

GCP knowledge

Regulatory compliance

Protocol troubleshooting

Source documentation

Medical records review

Education

Bachelor's degree in Health Sciences or related field

Job description

Prisma Health’s Upstate Administrative Research Staff in Greenville seeks a Clinical Research Coordinator to manage and oversee clinical trial studies, educate staff, and ensure data integrity and compliance across trials.

Responsibilities include coordinating patient visits, data collection, regulatory submissions, and communications with investigators and regulatory bodies; you’ll work with the health care team to ensure protocol adherence.