Clinical Research Nurse
About The Position
The Buck Institute is seeking a skilled and motivated Clinical Research Nurse to support human subject research studies conducted onsite. This role is responsible for executing study visits in accordance with research protocols while ensuring the safety, health, and welfare of research participants. The Clinical Research Nurse performs hands-on clinical procedures (including IV cannulation and blood draws), supports data collection, and supervises Research Associates. The role works closely with the Principal Investigator and research team to ensure studies are conducted in compliance with applicable federal, state, and local regulations, IRB approvals, and Buck policies.
Requirements
- Active California RN license (required)
- Diploma from an accredited nursing program required
- Bachelor’s degree in Nursing or related science preferred
- ACLS certification required
- Clinical nursing research experience preferred (not required for candidates eager to learn)
- Demonstrated competency in core nursing skills within the scope of practice (i.e., performing vital signs, nursing assessments, intravenous cannula insertion, etc.)
- Strong attention to detail and documentation accuracy
- Ability to work independently and as part of a collaborative research team
- Professional demeanor with strong communication and interpersonal skills
- Comfortable working under pressure, multitasking, and meeting deadlines
- Proficiency with basic IT systems (email, Word, Excel) or willingness to learn
- Familiarity with GCP, clinical trials, HIPAA, and regulatory requirements preferred
Nice To Haves
- Experience supporting individuals with diabetes
Responsibilities
- Conduct and document study visits in accordance with approved protocols
- Screen and interview potential participants; document medical history and eligibility
- Obtain and maintain informed consent throughout study participation
- Provide medical oversight during protocol-driven test visits
- Perform clinical procedures including vital sign monitoring, IV cannulation (advanced competency required), blood sample collection, and oral glucose tolerance tests
- Independently and efficiently perform IV insertions, including in challenging cases
- Collaborate with Clinical Research Associates on physical and cognitive testing
- Answer participant questions and provide study-related information during visits
- Communicate study-related issues to the Principal Investigator
- Support data collection in collaboration with researchers, statisticians, and lab staff
- Maintain strict confidentiality of all participant records and communications
Benefits
- 401k with 5% employer match after 1 year
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What This Job Offers
Job Type
Part-time
Career Level
Mid Level
Number of Employees
251-500 employees
