Clinical Research Coordinator II - Trials & Data

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

Job summary

Prisma Health in Greenville, SC seeks a dedicated Clinical Research Coordinator to manage day-to-day trial operations and ensure data quality. You will educate staff and care teams, coordinate data submission, monitor protocol compliance, and communicate updates to investigators and regulatory offices.

Responsibilities include developing data collection tools, supporting investigator-initiated studies, coordinating industry-sponsored trials, and maintaining high standards of documentation.

Qualifications

• Bachelor’s degree required.
• Two years of research experience in pharmaceutical, academic, device, NIH, investigator-initiated studies or registry trials.
• BLS certification within six months of employment preferred; driver’s license may be required in some roles.

Responsibilities

• Manage day-to-day study operations and contribute to program growth.
• Monitor study progress and ensure protocol and regulatory compliance.
• Educate research staff, healthcare team members, participants, and caregivers.
• Coordinate data collection, submission, and oversight of clinical data.
• Assist with protocol development, literature reviews, and data collection tools.
• Collaborate with Research Services and sponsors or local agencies on study documents and regulatory activities.
• Perform other duties as assigned.

Skills

GCP Knowledge

Regulatory Knowledge

Data Abstraction

Medical Records

Independent Work

Education

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

Job description

Prisma Health in Greenville, SC seeks a dedicated Clinical Research Coordinator to manage day-to-day trial operations and ensure data quality. You will educate staff and care teams, coordinate data submission, monitor protocol compliance, and communicate updates to investigators and regulatory offices.

Responsibilities include developing data collection tools, supporting investigator-initiated studies, coordinating industry-sponsored trials, and maintaining high standards of documentation.