Clinical Research Nurse (Decentralized Clinical Trials / DCV) – San Francisco, CA | ProPharma Careers
About ProPharma
ProPharma is a global consulting organization with over 20 years of experience supporting pharmaceutical, biotechnology, and medical device companies. Through its advise-build-operate model, ProPharma delivers comprehensive solutions across regulatory sciences, clinical research, pharmacovigilance, medical information, and quality & compliance. The company partners with clients to accelerate clinical development and improve patient outcomes through innovative, patient-centric approaches.
Job Overview
ProPharma is seeking a Clinical Research Nurse to support Decentralized Clinical Visits (DCVs) in and around San Francisco, California. This role involves delivering clinical trial services directly to patients outside traditional investigator sites, ensuring protocol compliance, patient safety, and high-quality data collection. Candidates must reside in or near San Francisco and be comfortable traveling locally for patient visits.
Job Location & Work Model
Location: San Francisco, California, USA (Local travel required)
Work Type: Field-based / Hybrid (patient-site visits)
Employment Type: Full-time
Key Responsibilities
Conduct decentralized clinical visits (DCVs) at patient locations (home, office, school, etc.)
Complete study-specific training including GCP, IATA (dangerous goods), and protocol-specific requirements
Collect and document clinical data following Good Documentation Practices (GDP)
Submit source documentation accurately and within defined timelines
Monitor and report patient safety concerns to study teams and investigator sites
Collaborate with clinical leadership to address complex clinical and operational challenges
Ensure readiness of equipment and supplies (e.g., centrifuge, ECG machine) for each visit
Maintain compliance with clinical research regulations and study protocols
Transport and handle clinical equipment as required
Required Skills and Competencies
Strong knowledge of clinical research and nursing practices
Ability to work independently in decentralized and patient-facing environments
Excellent organizational and multitasking skills
Strong communication skills (verbal and written)
Ability to adapt to schedule changes and travel with short notice
Proficiency in MS Office and willingness to learn proprietary eSource systems
High attention to detail and commitment to patient safety and data quality
Educational Qualifications
Registered Nurse (RN) with active, unrestricted US licensure
Multistate licensure preferred (where applicable)
Basic Life Support (BLS) Certification required
Experience Requirements
Minimum: 2+ years of post-graduate nursing experience
Freshers: Not eligible
Preferred: Experience in clinical research or decentralized clinical trials
Additional Requirements
Must reside in or near San Francisco, CA
Must have reliable transportation for patient visits and equipment transport
Ability to lift up to 25 lbs of clinical equipment
Must be legally authorized to work in the United States
Why Join ProPharma
Work on innovative decentralized clinical trial models
Direct patient interaction and impact on clinical research outcomes
Flexible, field-based working environment
Opportunity to collaborate with global clinical research teams
Exposure to advanced clinical trial technologies and processes
Diversity, Equity, and Inclusion
ProPharma is committed to creating an inclusive workplace where diversity is valued and employees are empowered to succeed. The organization fosters a culture of innovation, collaboration, and equal opportunity.
Application Process
All applications are reviewed directly by ProPharma’s recruitment team, ensuring a fair and transparent hiring process. Candidates will receive updates on their application status. ProPharma does not use AI-based screening tools.
Important Notice
ProPharma does not accept unsolicited resumes from third-party recruiters. Direct inquiries via phone or email regarding this role are not permitted.
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