Research Coordinator II, Clinical Research, Full Time, Days

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

Inspire health. Serve with compassion. Be the difference.

Job Summary

Responsible for the implementation and day-to-day management of clinical trial research studies, including educating research staff, health care team members, participants, and caregivers. Coordinates the collection, submission, and oversight of clinical data; monitors protocol compliance; and maintains systems to support accurate and timely data flow. Manages participant visits and carries out protocol required procedures. Monitors participant progress and safety, and communicates relevant updates to investigators, regulatory offices, the health care team, and study staff.

Essential Functions

• All team members are expected to be knowledgeable and compliant with Prisma Health’s purpose: Inspire health. Serve with compassion. Be the difference.
• Manages study operationsby coordinatingday todaystudyoperationsand developing strategies to contribute tothe programgrowth.
• Monitorsstudy progress andmaintainscompliance with protocols and regulations
• Supportsinvestigator-initiatedstudies byassistingwith protocol development, literature reviews, and creation of data collection tools. Coordinatesindustry sponsoredclinical trials by implementingsponsor providedprotocols, completing required regulatory submissions, and ensuring adherence to study procedures and timelines.
• Assistsincoordinatingresources to conduct trialsincluding the development of data collection toolsandcommunication with ancillary departments to implement study related procedures.
• Collaborates withResearch Services officesandsponsoringor local agencies tosubmitrequiredstudy documents and ensure awareness of study progress, amendments, and regulatory activities.
• Performs other duties as assigned.

Supervisory/Management Responsibilities

• This is a non-management job that will report to a supervisor, manager, director or executive.

Minimum Requirements

• Education - Bachelor’s Degree in Health Sciences or Business-related field of study.
• Experience - Two (2) years of research experience in at least one of the following areas: pharmaceutical, academic, device, National Institute of Health(NIH), investigator-initiated studies or registry trials.

In Lieu Of

• In lieu of education and experience noted above an equivalent combination of work experience and academic experience may be considered.

Required Certifications, Registrations, Licenses

• BLS is required within six (6) months of employment.
• Collaborative Institutional Training Initiative (CITI) preferred.
• If Allied Health Degree: State certification/license in field.
• Some team members may be required to have a valid driver’s license to perform the essential functions of the role. In these situations, an acceptable motor vehicle record as defined by the Acceptable Motor Vehicle Record (MVR) Chart, and proof of auto insurance is required.

Knowledge, Skills and Abilities

• Ability to applyGood Clinical Practice (GCP)principlesindependently across studies
• Knowledgeof clinical research regulationsto daily operations
• Ability toapplyprotocol requirementsandtroubleshoot visit issues
• Ability to effectively use specialty‑specific terminology
• Ability toindependently interpret medical records with minimalassistance
• Ability to independently manage quality dataabstractionandensure high-quality sourcedocumentation standards
• Ability tomaintainongoing professional development byparticipatingin seminars, workshops, in-servicetrainings, and by staying current with relevant literature and emerging trends in the field.

Work Shift

Day (United States of America)

Location

Cancer Centers - Faris Road

Facility

Greenville Memorial Hospital

Department

Clinical Research Unit-CIF