Clinical Research Associate Jobs in South Carolina, United States

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.

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.

Join a global clinical research organization that has supported the top 50 pharmaceutical companies and 750+ biotechs across 2,700 trials in 100+ countries. As an Assistant Clinical Research Associate, you will perform remote activities on assigned projects in liaison with the CRA and study Clinical Lead, providing support with site preparedness, logistical support to the monitoring process, and assisting with site management and remote monitoring tasks per SOPs and regulatory guidelines.

FSP team at Covance seeks Senior Clinical Research Associate 2 to lead monitoring of in‑vitro diagnostics trials across the US. The role conducts site monitoring, data verification, SAE reporting and supports site staff training while ensuring protocol compliance. Remote work from any US location with 50‑60% overnight travel required.

Research Services - Clinical Research Management at Prisma Health ensures research contracts are compliant and executed efficiently. The Research Contract Specialist reviews, edits, negotiates, and tracks research agreements, collaborating with sponsors, legal, IT, and purchasing teams.

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.

Office of Clinical Research (OCR) at Medical University of South Carolina manages industry-sponsored clinical trial budgeting and negotiations. The manager leads internal budget development, negotiates sponsor budgets, and drives continuous improvement of the OCR fee‑for‑service program.

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.

Alcanza Clinical Research, a multi-site clinical research organization, conducts Phase I-IV studies across therapeutic areas such as vaccines and neurology. The Clinical Research Coordinator ensures study execution by screening patients, obtaining consents, collecting vital signs and specimens, entering data into EDC systems, and maintaining regulatory compliance.

Alcanza is a multi-site clinical research company conducting Phase I-IV studies across various therapeutic areas. The Research Assistant supports Clinical Research Coordinators and investigators by performing clinical, lab, and administrative tasks to ensure site operations run successfully.

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

Headlands Research seeks a Clinical Research Assistant to support clinical trial execution at the Trial Management Associates site in Myrtle Beach, SC. The role involves assisting coordinators with subject screening, data entry, and vital sign collection to advance healthcare treatments. This is a full-time position operating on a hybrid work model.

Care Access Research team advances community health by conducting clinical trials and health screenings. The Clinical Research Assistant supports patient coordination, specimen handling, and regulatory compliance while learning to become a Clinical Research Coordinator.

Alcanza Clinical Research, a multi-site clinical research company, conducts Phase I‑IV studies across therapeutic areas such as vaccines and neurology. The Clinical Research Assistant supports Coordinators and investigators by screening patients, collecting vitals and specimens, entering data into EDC, and maintaining study documentation.

StrideCare Clinical Research team coordinates and conducts clinical studies at its Charleston, SC site. The CRC screens patients, obtains consent, schedules visits, collects vital signs, ECGs and specimens, enters data into EDC systems, and ensures regulatory compliance and safety reporting.

Lowcountry Urology clinical research team conducts urology trials to advance patient care. The coordinator manages study protocols, collects and enters data, handles specimen logistics, and ensures regulatory compliance while interacting directly with patients and sponsors.

Alcanza Clinical Research, a multi-site clinical research company, conducts Phase I-IV studies across therapeutic areas. The Clinical Research Assistant supports coordinators and investigators with patient screening, data entry, specimen handling, and study logistics.

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.

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