Clinical Research Associate Jobs in South Carolina, United States

Clinical Operations at Worldwide Clinical Trials drives innovative clinical research across therapeutic areas. The Senior Clinical Research Associate, CNS, manages site activities from start‑up through close‑out, conducts initiation visits, ensures regulatory compliance, and supports data collection remotely while traveling regionally as needed.

Fortrea's FSP team is hiring experienced Clinical Research Associates (CRAs) specializing in Ophthalmology monitoring across major US hub locations. The role involves full-cycle study site monitoring, CRF review, SAE reporting, and ensuring participant safety and data integrity in a fast-paced, technology-driven clinical research environment.

Summary of the Position: The Associate Director of Clinical Affairs will be responsible for all downstream clinical activity and technical collateral. This will include oversight of Professional Service Veterinarians (PSV), Field Service Veterinarians (FSV), and key opinion leader (KOL) management.

As a Clinical Research Associate (CRA) at Worldwide, you will find yourself working alongside brilliant minds across diverse therapeutic areas, including Cardiovascular, Metabolic, Neuroscience, Oncology, and Rare Diseases. Collaboration with top-tier colleagues from various backgrounds and specialties is not just encouraged; it's ingrained in our culture.

Our FSP team is currently seeking experienced CRA 2s located near major hub airports across the US with 2 years of monitoring! 8-10 days on site per month being a mix of onsite and remote.

Our FSP team is currently seeking a CRA 2 with 2 years of monitoring! 8-10 days on site per month being a mix of onsite and remote.

Our FSP team is currently seeking Oncology CRA 2s in Southeast Region! 8-10 days on site per month being a mix of onsite and remote.

The Medical University of South Carolina’s Office for Clinical Research seeks a Sponsor Invoicing Analyst to support industry-sponsored study billing and reconciliation. This role coordinates invoicing activities, analyzes contracts, and provides training on clinical trial management systems to ensure revenue realization.

Prisma Health seeks a Registered Nurse for its Clinical Research Unit to implement and oversee clinical trials at Greenville Memorial Hospital. The role involves patient screening, data management, protocol compliance, and staff supervision within an on-site setting in Greenville, SC. This full-time position supports the organization's mission to transform healthcare through compassionate service.

IQVIA is a global leader in advanced analytics, technology solutions, and clinical research services, partnering with pharmaceutical, biotechnology, and medical device companies to improve patient outcomes and accelerate innovation. As a Clinical Research Coordinator in Union, SC, you will support clinical research studies under a principal investigator, performing hands-on clinical procedures such as ECG, sample collection, and vital signs, coordinating studies, and ensuring compliance with pro

ObjectiveHealth is a clinical research company using proprietary technology to increase patient access to research trials, provide physicians with enhanced care options, and deliver superior clinical research enrollment metrics to Pharma sponsors, with the goal of improving patient outcomes at the point of care. The Clinical Research Coordinator II will take ownership of assigned studies and patients, conduct clinic visits, perform direct patient care activities, manage regulatory compliance and

Headlands Research Clinical Research team supports clinical trial delivery across community sites, leveraging technology and support services to expand patient participation. Clinical Research Assistants help execute trials by assisting with study visits, preparing materials, collecting and organizing data, and ensuring protocol compliance while interacting directly with patients and care teams.

The Registered Nurse (RN) - Clinical Research - Oncology - St. Francis Cancer Center serves as RN Research (Exempt) Clinical Research Nurse Coordinator for Bon Secours Cancer Institute. This role enrolls patients in research studies, organizes and monitors clinical research observational and data collection studies, and serves as liaison between Bon Secours Cancer Institute, area hospital departments, and sponsoring agencies for multiple clinical trials.

Headlands Research Clinical Research team advances new therapies by managing patient-focused clinical trials across a growing network of sites. Coordinators support day-to-day trial execution, including patient interactions, study visit scheduling, data collection, and regulatory compliance while collaborating with investigators and cross‑functional teams.

Alcanza is a growing multi-site, multi-phase clinical research company with a network of locations in AL, AZ, FL, GA, IL, MA, MI, MO, NV, VA, SC, TN, TX and Puerto Rico. We have established a strong presence across Phase I-IV studies and several therapeutic areas including vaccine, neurology, dermatology, psychiatry, and general medicine.

Our clinical research company is looking to hire a qualified candidate for the full-time position of Clinical Research Coordinator. The ideal candidate will possess certification such as an MA, phlebotomy, or similar and have a strong desire to work directly with patients.

The Clinical Research Coordinator (CRC) works to ensure the execution of assigned studies in compliance with GCP, ICH, HIPAA, FDA Regulations and SOPs.

The Research Assistant (RA) provides support to the Clinical Research Coordinators (CRCs), Site Manager, Principal and Sub Investigators, and other site staff in compliance with GCP, ICH, HIPAA, FDA Regulations and SOPs. The RA performs clinical, lab, and administrative tasks as needed for the successful operation of the clinical research site.

Clinical Research Coordinator works under Clinical Research Managers and are tasked with administering clinical trials. Responsibilities include managing clinical trials and collecting data, informing participants about study objectives, and administering questionnaires.

This is a remote central research administration position reporting to the Associate Director, Clinical Trial Management Systems within the Office of Clinical Research (OCR) under the Office of the Vice President for Research. The Clinical Research Analytics & Systems Analyst serves as the primary resource for clinical research metrics, reporting, analytics, and data visualization across the research enterprise.