What are the responsibilities and job description for the Clinical Research Coordinator position at Palmetto Clinical Trial Services, LLC?
Company Description
Palmetto Clinical Trial Services, LLC is a leading multicenter clinical research site located in the Greenville/Anderson, South Carolina area. With two advanced sites, the organization provides access to cutting-edge technologies and treatments to the local community. Palmetto Clinical is driven by a dedicated and experienced team, focused on maintaining the highest standards in clinical study conduct. The team is committed to delivering exceptional care and support to all patients participating in clinical trials.
Role Description
This is an on-site role for a Clinical Research Coordinator, based in Anderson, SC. The Clinical Research Coordinator will coordinate and oversee the execution of clinical trials, ensure adherence to research protocols, obtain informed consent from participants, and manage the day-to-day operations related to clinical studies. Responsibilities also include working collaboratively with investigators and maintaining accurate and organized documentation in compliance with regulatory standards.
Qualifications
- Experience and knowledge of Clinical Research and Clinical Trials management is preferred
- Proficiency in understanding and implementing Protocols and conducting Research is preferred
- Ability to obtain and manage Informed Consent from participants ethically and effectively
- Attention to detail, organizational skills, and strong verbal and written communication abilities
- Familiarity with federal regulations and Good Clinical Practice (GCP) guidelines is preferred
- Flexibility to work on-site in Anderson, SC
- CMA (Certified Medical Assistant) or RMA (Registered Medical Assistant) required