- San Antonio, Texas, United States
- On-site
- Entry
- 1–2 years
Deliver clinical research operations work, support clinical trials, ensure protocol adherence, and provide patient care.
Responsibilities
- Assist in planning, implementation, and coordination of clinical research activities per study protocols
- Conduct patient assessments, administer study treatments, and perform clinical procedures
- Collect, record, and maintain accurate data documentation in eCRFs and study databases
- Collaborate with multidisciplinary teams to ensure efficient study conduct and participant recruitment
- Provide education and counseling to study participants and families
Requirements
- Bachelor's degree in Nursing (BSN)