Position Overview
Valiance Clinical Research is seeking contract Nurse Practitioners to support our clinical research operations by supplementing the Sub-Investigator (Sub-I) role. This is a great opportunity for experienced NPs who are interested in contributing to clinical trials and supporting participant safety, protocol compliance, and high-quality clinical data collection.
This role is contract-based and ideal for clinicians seeking flexible shifts and meaningful work in advancing medical research.
Key Responsibilities
- Support the Principal Investigator (PI) and research team with study-related clinical oversight
- Perform and document study visits, including assessments and clinical evaluations as delegated
- Conduct medical history reviews, symptom checks, and focused physical assessments
- Assist with eligibility confirmation per protocol inclusion/exclusion criteria
- Evaluate and document adverse events (AEs) and serious adverse events (SAEs) in collaboration with the PI
- Provide clinical review of lab results, vitals, ECGs, and concomitant medications as applicable
- Ensure documentation meets GCP, ICH, protocol, and regulatory requirements
- Collaborate with CRCs and site staff to support visit flow and subject safety
- Participate in training on protocol-specific requirements and site processes
Required Qualifications
- Active Nurse Practitioner license in California (in good standing)
- National certification (AANP or ANCC)
- Minimum [1+] years of clinical experience (primary care, urgent care, internal medicine, etc. preferred)
- Comfortable performing clinical evaluations and making medical determinations within scope
- Strong documentation skills and attention to detail
- Professional communication and ability to work collaboratively with clinical research teams
- Reliable availability for flexible scheduling as study needs arise
Preferred Qualifications
- Prior experience in clinical research (Sub-I, PI extender, research clinician, etc.)
- Familiarity with GCP / ICH guidelines and clinical trial documentation
- Experience with eSource/EDC systems and EMRs
- Bilingual (English/Spanish) a plus
- Experience in specialty areas such as Nephrology / Cardiology / Pulmonology / Internal Medicine / Family Medicine depending on trial portfolio
Why Work With Us
- Flexible contract schedule
- Opportunity to participate in cutting-edge clinical research
- Supportive research team environment
- Competitive contract compensation
- Training provided for study-specific responsibilities
Additional Details
- Work performed primarily on-site at our clinical research facility
- Must be able to pass background checks and comply with sponsor/site onboarding requirements
- HIPAA compliance and strict confidentiality required
How to Apply
Please submit your resume and availability. Candidates may be asked to provide:
- NP license and certification documentation
- CV (research format preferred)
- Proof of malpractice coverage (or willingness to obtain)
- List of prior clinical research experience (if applicable)
Pay: $75.00 - $85.00 per hour
Expected hours: 10 – 20 per week
Work Location: In person
