Current BLS certification; ACLS or other certifications as required.
3+ years of clinical nursing experience in relevant settings such as research or oncology.
Strong assessment and documentation skills.
Ability to navigate protocol and medical governance boundaries.
Responsibilities
Conduct participant assessments and clinical procedures as per protocol.
Administer medications or investigational products under authorized conditions.
Review visit readiness and ensure all necessary documentation is in place.
Identify and escalate safety concerns and protocol deviations promptly.
Maintain accurate source documentation in clinical systems.
Coordinate with various stakeholders including investigators and participants.
Support informed-consent discussions and verify consent documentation.
Ensure compliance with training, licensure, and emergency-readiness requirements.
Benefits
Medical, dental, and vision insurance with significant employer contributions.
Basic life insurance provided by the company, with optional supplemental coverage.
Employer-paid disability insurance at 50%.
401k plan with a generous 10% 1:1 match.
10 days of PTO plus companywide paid holidays.
Reimbursement for carpooling, clean air vehicles, and cell phone expenses.
Employee rewards and recognition program to celebrate achievements.
Opportunities for social events and team-building activities.
Full Job Description
Yowei Therapeutics is seeking a California Registered Nurse to support protocol-driven clinical research and longevity programs under appropriate medical, protocol, and site oversight.
Job Duties:
Conduct protocol- and scope-authorized participant assessments, visits, education, vital signs, medication reconciliation, specimen collection, and clinical procedures.
Administer medications or investigational products only when authorized by applicable law, protocol, orders, delegation, training, and site procedures.
Identify and promptly escalate adverse events, safety concerns, protocol deviations, abnormal findings, and participant questions to the appropriate qualified clinician or study owner.
Maintain accurate, timely source documentation and required entries in approved clinical and operational systems.
Coordinate with investigators, NPs, CRCs, pharmacy, laboratories, imaging providers, sponsors, and participants.
Support informed-consent discussions without replacing the investigator's responsibilities and verify required consent documentation before procedures.
Maintain training, competency, licensure, certifications, privacy, infection-control, and emergency-readiness requirements.
Support visit scheduling, follow-up, data-query resolution, supply accountability, and inspection readiness.
Requirements
Active, unrestricted California RN license.
Current BLS certification; ACLS or other certifications as required by the final procedures and site model.
3+ years of clinical nursing experience in research, infusion, ambulatory care, oncology, endocrinology, wellness, or another relevant setting.
Strong assessment, documentation, participant communication, and escalation skills.
Ability to work within protocol, licensure, delegation, privacy, and medical-governance boundaries.
Benefits
Medical, dental, and vision insurance (Kaiser HMO or BlueShield PPO. Employer pays 85% for Employee and 50% for Employee's family; Dental: Aetna Dental, Delta Dental, Guardian Dental, MetLife Dental. Vision: VSP and Aetna EyeMed)
Basic life ($20,000 paid by company) and supplemental life insurance (optional supplemental).
Disability insurance 50% standard employer paid.
401k 10% 1:1 match
PTO policy. 10 days PTO
Companywide paid holiday during: Week of July 4, Thanksgiving (2 days), Week of December 25
Carpool, clean air vehicle, and cell phone reimbursement
