- ThermoFisher Scientific (Greenville, NC)
- …Standard (Mon-Fri) **Environmental Conditions** Office **Job Description** **Job Summary** As the GCP Compliance and Process Lead at Thermo Fisher Scientific, ... + Solid knowledge of drug development, clinical trial management, and/or GCP compliance processes + Proven awareness of sponsor oversight requirements… more
- Gilead Sciences, Inc. (Foster City, CA)
- …Operations organization. + Collaborate with Clinical Operations to confirm adherence to GCP compliance execution through all stages of clinical trial conduct ... Operations. The Associate Director will be a key member of the Connect GCP Excellence and Inspection Readiness (GEIR) team and collaborate with Clinical Operations… more
- Takeda Pharmaceuticals (Boston, MA)
- …Management and Statistics, with at least 3 years of experience in GCP Quality/ Compliance . + Advanced knowledge of pharmaceutical development, medical affairs ... the role:** The Associate Director, Clinical & Quality Process Compliance is responsible for ensuring the quality of processes...and GCP /GVP regulations including FDA, EU, MHRA, PMDA and ICH.… more
- System One (Diamondhead, MS)
- …+ Supervise sub-investigators, research coordinators, and clinical staff to ensure GCP compliance . + Oversee investigational product management, including drug ... This PRN role ensures that all study activities are performed in compliance with ICH- GCP , FDA, and institutional standards, prioritizing participant safety,… more
- ManpowerGroup (Greenwood Village, CO)
- …including VPCs, subnets, and firewall rules. + Implement security best practices and compliance standards within the GCP network infrastructure. + Develop and ... successfully in the organization. **Job Title:** Principal Network Engineer (Architect with GCP knowledge) **Location:** Onsite 4 days a week in Greenwood Village,… more
- System One (Walnut Creek, CA)
- …+ Supervise sub-investigators, research coordinators, and clinical staff to ensure GCP compliance . + Oversee investigational product management, including drug ... This PRN role ensures that all study activities are performed in compliance with ICH- GCP , FDA, and institutional standards, prioritizing participant safety,… more
- System One (Concord, NC)
- …the study. + Supervise sub-investigators, coordinators, and site staff to ensure GCP compliance . + Oversee investigational product management and documentation. ... site. This position ensures trials are executed in accordance with ICH- GCP , FDA, and institutional standards, maintaining participant safety and scientific… more
- System One (Lindenwold, NJ)
- …with respiratory conditions. + Supervise sub-investigators and clinical staff; ensure GCP compliance . + Oversee study drug accountability and documentation. ... studies. This PRN role ensures all research activities are performed in compliance with regulatory, ethical, and scientific standards and that subject safety is… more
- Vitalief (Phoenix, AZ)
- …staff. + Provide ongoing training and guidance to site teams on study procedures, GCP compliance , and protocol adherence. CRO & Vendor Oversight + Provide ... Document Verification (SDV) and ensure data accuracy, completeness, and protocol compliance . + Review clinical documentation (eg, CRFs, monitoring plans, data… more
- Takeda Pharmaceuticals (Boston, MA)
- …Management and Statistics, with at least 3 years of experience in GCP Quality/ Compliance . + Advanced knowledge of pharmaceutical development, medical affairs ... Clinical Program Quality Investigations is responsible for ensuring the compliance of deviation management and serious breach process. This...and GCP /GVP regulations including FDA, EU, MHRA, PMDA and ICH.… more
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