What are the responsibilities and job description for the Clinical Research Assistant position at Santé Clinical Research?
Company Description Santé Clinical Research is a clinical research organization based in Kerrville, Texas, at 1208 Bandera Highway. The company focuses on supporting clinical studies that advance medical knowledge and improve patient care. Team members work closely with investigators, healthcare professionals, and participants to ensure high-quality data collection and ethical study conduct. The organization values accuracy, regulatory compliance, and collaboration in all aspects of clinical research.
Role Description This is an on-site Clinical Research Assistant contract role located in Kerrville, TX. The Clinical Research Assistant will support clinical trials by assisting with participant screening, scheduling, and visit coordination, as well as maintaining accurate source documents and study records. Daily tasks include collecting and recording clinical data, preparing and organizing study materials, and performing basic laboratory-related procedures according to protocol and safety guidelines. The role also involves communicating with participants and study staff, helping ensure adherence to regulatory requirements and study protocols, and supporting the principal investigator and clinical research coordinators in day-to-day operations.
Qualifications
Role Description This is an on-site Clinical Research Assistant contract role located in Kerrville, TX. The Clinical Research Assistant will support clinical trials by assisting with participant screening, scheduling, and visit coordination, as well as maintaining accurate source documents and study records. Daily tasks include collecting and recording clinical data, preparing and organizing study materials, and performing basic laboratory-related procedures according to protocol and safety guidelines. The role also involves communicating with participants and study staff, helping ensure adherence to regulatory requirements and study protocols, and supporting the principal investigator and clinical research coordinators in day-to-day operations.
Qualifications
- Candidates should possess strong Interpersonal Skills and Communication abilities to interact effectively with participants, investigators, and team members.
- Candidates should possess knowledge of Medical Terminology relevant to clinical research and patient care settings.
- Candidates should possess Research skills, including data collection, documentation, and adherence to protocol-driven procedures.
- Candidates should possess basic Laboratory Skills such as handling specimens, following safety procedures, and using standard equipment under supervision.
- Attention to detail and strong organizational skills for accurate record-keeping and time management.
- Ability to follow written protocols, regulatory guidelines, and quality standards in a clinical environment.
- Proficiency with basic computer applications and electronic data capture systems.
- Relevant education in a health, life science, or related field; prior clinical research or healthcare experience is preferred but not required.