About the Company
Gilead Sciences, Inc. is a biopharmaceutical company that discovers, develops, and commercializes innovative medicines in areas of unmet medical need. We strive to transform and simplify care for people with life-threatening illnesses around the world. With a strong commitment to scientific excellence and patient impact, Gilead is at the forefront of medical innovation, working to create a healthier world for everyone.
Job Description
Gilead Sciences is seeking a dedicated and experienced Research Nurse to join our dynamic clinical trials team in Warm Springs, Fremont, CA. In this critical role, you will be instrumental in the planning, coordination, and execution of clinical research studies, ensuring the highest standards of patient care and data integrity. You will work closely with investigators, study coordinators, and other healthcare professionals to manage study participants, administer experimental treatments, and monitor for adverse events, all while adhering strictly to study protocols, GCP guidelines, and regulatory requirements. This is an exciting opportunity to contribute directly to the advancement of life-saving therapies within a leading global pharmaceutical company.
Key Responsibilities
- Recruit, screen, and enroll eligible study participants according to protocol criteria.
- Provide direct patient care, including administering investigational drugs and performing study-related assessments (e.g., vital signs, EKGs, venipuncture).
- Monitor participants for adverse events, assess severity, and report findings to investigators and sponsors as required.
- Educate participants and their families about the clinical trial process, potential risks, and benefits.
- Maintain accurate and comprehensive study documentation, including source documents, case report forms (CRFs), and electronic data capture (EDC) systems.
- Ensure compliance with FDA regulations, ICH-GCP guidelines, HIPAA, and institutional policies.
- Assist with the preparation for and conduct of study monitoring visits and audits.
- Collaborate effectively with interdisciplinary teams, including physicians, pharmacists, and research coordinators.
- Manage investigational product accountability and storage.
Required Skills
- Active Registered Nurse (RN) license in the state of California.
- Minimum of 2 years of clinical nursing experience, preferably in an acute care setting.
- Strong understanding of clinical research principles, including ICH-GCP guidelines and FDA regulations.
- Excellent patient assessment and critical thinking skills.
- Proficiency in medical terminology and clinical documentation.
- Exceptional organizational and time management abilities.
- Strong interpersonal and communication skills.
- Ability to work independently and as part of a collaborative team.
Preferred Qualifications
- Bachelor of Science in Nursing (BSN).
- Certified Clinical Research Coordinator (CCRC) or Certified Clinical Research Professional (CCRP) certification.
- Experience with Electronic Data Capture (EDC) systems.
- Previous experience as a Research Nurse or Clinical Research Coordinator in a pharmaceutical or biotech setting.
- Experience with oncology, virology, or inflammatory disease clinical trials.
Perks & Benefits
- Comprehensive medical, dental, and vision insurance plans.
- Generous paid time off and holiday schedule.
- 401(k) retirement plan with company match.
- Employee stock purchase program.
- Tuition reimbursement and professional development opportunities.
- Wellness programs and on-site fitness facilities.
- Life and disability insurance.
- Flexible spending accounts.
How to Apply
If you are interested in this position, please click the "Apply Now" button below. To ensure your application is properly considered, please prepare the following:
- An up-to-date Resume or CV
- A brief cover letter summarizing your experience and motivation
Applications are reviewed on a rolling basis. Only shortlisted candidates will be contacted for an interview.
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