- Takeda Pharmaceuticals (Austin, TX)
- …innovation-driven company to inspire you and empower you to shine? Join us as an Associate Director , GCP Compliance based remotely reporting to the ... Director , GCP Compliance . At Takeda, we are transforming the pharmaceutical industry through our R&D-driven market leadership and being a values-led company.… more
- Takeda Pharmaceuticals (Juneau, AK)
- …company to inspire you and empower you to shine? Join us as an Associate Director , GCP Excellence in Clinical Trials based remotely reporting ... to the Director , GCP Excellence in Clinical Trials. At...ways of working. + Partner with R&D Quality and GCP Compliance Management to develop GCP… more
- Takeda Pharmaceuticals (Des Moines, IA)
- …as a Manager, GCP Excellence in Clinical Trials based remotely reporting to the Associate Director , GCP Excellence in Clinical Trials. At Takeda, we are ... representing GCP Excellence globally, assisting in implementing GCP Excellence processes to enhance support and compliance... GCP Excellence processes to enhance support and compliance . + Act as subject matter expert for operating… more
- Novo Nordisk (Plainsboro, NJ)
- …to the head of Clinical, medical, Regulatory (CMR) Business Operations, the Associate Director (AD) is responsible for structuring facilitating and monitoring ... and other key internal stakeholders. In the execution of specific projects, the Associate Director , will be accountable for managing relationships with internal… more
- Takeda Pharmaceuticals (Providence, RI)
- …both sponsor and investigator sites. **ACCOUNTABILITIES:** + Provide expertise in GCP compliance interpretation, consultation, training, and recommendations to ... lead clinical development teams in preparation for announced inspections and provide GCP compliance technical support during inspections of investigator sites… more
- Teva Pharmaceuticals (West Chester, PA)
- Associate Director , Global Clinical Quality Date: Feb 5, 2025 Location: West Chester, United States, Pennsylvania, 19380 Company: Teva Pharmaceuticals Job Id: ... management activities, and leads continuous improvement for clinical development activities. The Associate Director - Global Clinical Quality leads a portfolio… more
- Regeneron Pharmaceuticals (Basking Ridge, NJ)
- We are seeking an Associate Director to join out Oncology Clinical Development department. The Associate Director Clinical Sciences leads in the ... of study data of a clinical development program. The Associate Director leads in a matrix environment...compliance in accordance with FDA, EMEA, ICH and GCP guidelines as well as applicable SOPs regarding clinical… more
- Bristol Myers Squibb (Princeton, NJ)
- …in their personal lives. Read more: careers.bms.com/working-with-us . **Position Summary** The Associate Director of Specialty Laboratory Vendor Quality will be ... mainly responsible for implementing the strategy for GCP /GCLP/GLP specialty laboratory (ie, biomarker) vendors from a quality perspective and delivering the full… more
- Regeneron Pharmaceuticals (Tarrytown, NY)
- We are seeking an Associate Director to join our Clinical Development team. The Associate Director Clinical Sciences leads in the development, ... and deliver on clinical studies and programs. **As an Associate Director , a typical day may include...compliance in accordance with FDA, EMEA, ICH and GCP guidelines as well as applicable SOPs regarding clinical… more
- Bristol Myers Squibb (Summit, NJ)
- …in their personal lives. Read more: careers.bms.com/working-with-us . **Position Summary** The Associate Director , Therapeutic Area Audit Strategy Lead will be ... the central QMS team + Lead the Quality and Compliance R&D Escalation Process + Ensure GLP systems are...of vendors and manage external Quality Systems + Execute GCP and Pharmacovigilance audits and support GCP … more