Skill
Good Clinical Practice
Healthcare and Medical
Good Clinical Practice (GCP) is an internationally recognized set of ethical and scientific quality standards, established by the ICH (International Council for Harmonisation), for designing, conducting, recording, and reporting clinical trials involving human subjects. It ensures the rights, safety, and well-being of trial participants are protected while guaranteeing the credibility of clinical trial data. GCP certification is commonly required for clinical research coordinators, investigators, and pharmaceutical/biotech professionals involved in drug and medical device trials.
Good Clinical Practice in the job market
Last checked October 28, 2026
- Open roles
- 5
- Employers
- 3
- Median pay
- —
- Disclose pay
- —
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Open roles requiring Good Clinical Practice (5)
Oncology Clinical Research Associate (CRA 2), Sponsor Dedicated
IQVIA
$71,900 – $182,000
IQVIA is seeking a Clinical Research Associate to oversee oncology trial sites, managing monitoring visits, regulatory compliance, and data integrity across US locations. This role suits candidates with 1-2 years of clinical research monitoring experience who can coordinate between study teams and research sites to ensure protocol adherence and timely enrollment.
Listed on IQVIA’s careers site · Apply there ↗
Clinical Trial Monitor
Bristol Myers Squibb
Bristol Myers Squibb is seeking a Clinical Trial Monitor to oversee the conduct, documentation, and regulatory compliance of clinical trials across multiple sites and therapeutic areas. This role suits healthcare professionals with clinical research experience who are comfortable with independent site management, regulatory oversight, and travel-based work.
Listed on Bristol Myers Squibb’s careers site · Apply there ↗
Clinical Program Manager
Gilead Sciences
Full-time · United States - California - Foster City · $165,495 – $235,620
This role manages the end-to-end execution of clinical trials across multiple therapeutic areas at a pharmaceutical company, overseeing budgets, timelines, vendor relationships, and cross-functional teams while ensuring regulatory compliance. It suits experienced professionals in clinical operations who want to drive large-scale research programs and develop leadership capabilities.
Listed on Gilead Sciences’s careers site · Apply there ↗
Director, Medical Safety- Sponsor-Dedicated (Home-based)
IQVIA
This role oversees medical safety and pharmacovigilance for a CRO's client programs, reviewing trial data and regulatory documents while leading a team of physicians and safety professionals. It suits experienced medical safety physicians who want to manage complex, multi-stakeholder projects with both clinical and people leadership responsibilities.
Listed on IQVIA’s careers site · Apply there ↗
Director, Clinical Development (MD)
Gilead Sciences
Full-time · United States - California - Foster City · $261,375 – $338,250
This role leads clinical development programs for inflammation and fibrosis therapies at a major biopharmaceutical company, overseeing trial design, regulatory submissions, and cross-functional coordination. It suits physicians with significant drug development experience who want to shape late-stage therapeutic programs while providing medical oversight.
Listed on Gilead Sciences’s careers site · Apply there ↗
Roles that use Good Clinical Practice
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