- Novo Nordisk Inc. (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
- Merck & Co. (Rahway, NJ)
- …- Knowledge of Good Manufacturing Practices (GMP) and Good Clinical Practices ( GCP ) is highly desirable. - Preferred Experience and Skills: - - Proficiency ... consider qualified applicants with arrest and conviction records for employment in compliance with the San Francisco Fair Chance Ordinance Los Angeles Residents… more
- Takeda Pharmaceuticals (Trenton, NJ)
- …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 (Trenton, NJ)
- …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 (Trenton, NJ)
- …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
- Bristol Myers Squibb (New Brunswick, NJ)
- …their personal lives. Read more: careers.bms.com/working-with-us . **Position Summary** The Associate Director of Specialty Laboratory Quality is responsible for ... effective management of the GLP/GCLP/ GCP specialty laboratory audit program, with an emphasis on risk-based management, regulatory strategy development (ie,… 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 (New Brunswick, 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
- Bristol Myers Squibb (New Brunswick, 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
- Regeneron Pharmaceuticals (Basking Ridge, NJ)
- The Associate Director , Vendor Management, is responsible for assessing, onboarding, and overseeing the health and performance of vendors involved in clinical ... execution. This role ensures that vendors meet the necessary qualifications and compliance standards, manage relationships, and oversee delivery to time, cost, and… more
- Bristol Myers Squibb (New Brunswick, NJ)
- …and in their personal lives. Read more: careers.bms.com/working-with-us . Position Summary The Associate Director , RBQM - HOCT, ICN will mainly be responsible ... vendors, demonstrating effective risk and issue management. Provide quality and compliance consultation to clinical trials teams throughout study lifecycle and… more
- Merck (Trenton, NJ)
- **Job Description** **Role Summary** + The Oncology Regional Medical Scientific Director ( Associate RMSD) is a credentialed (ie, PhD, PharmD, DNP, MD) ... including field standard operating procedures (SOPs), Good Clinical Practice ( GCP ) guidelines, and administrative/operational responsibilities **Preferred** + Field-based medical… more
- Kyndryl (New York, NY)
- …world for our employees, our customers and our communities. **The Role** As a Associate Director , Client Solutions Advisor, you will apply your knowledge of ... cloud experience using native services in AWS, Azure and/or GCP + 8+ years of experience as an engineer...status, or other characteristics. Kyndryl is also committed to compliance with all fair employment practices regarding citizenship and… more
- Merck (Rahway, NJ)
- …+ Knowledge of Good Manufacturing Practices (GMP) and Good Clinical Practices ( GCP ) is highly desirable. **Preferred Experience and Skills:** + Proficiency in using ... consider qualified applicants with arrest and conviction records for employment in compliance with the San Francisco Fair Chance Ordinance **Los Angeles Residents… more
- SMBC (New York, NY)
- …to Haves * Azure Certifications - Solutions Architect, AWS Security Specialty * GCP Certifications - Associate Cloud Engineer, Professional Security Engineer * ... portfolio of benefits to its employees. **Role Description** The Director of Cloud Security Architecture will ensure bank's cloud...and reporting on cloud security issues across our AWS, GCP , and Azure environments. This role is responsible for… more
- Mount Sinai Health System (New York, NY)
- …and monitors all safety aspects of clinical research trial(s). Under guidance of the Associate Director of Research and Quality Outcomes, the CRA is responsible ... **Job Description** The Clinical Research Associate is an integral part of the research...reporting, CEC and DSMB of clinical studies to ensure compliance with regulations and guidelines. The CRA also collects,… more
- Mount Sinai Health System (New York, NY)
- …of the research program. The Clinical Program Manager will report into the Associate Director , Myeloma Translational Research. The CPM will primarily provide ... Clinical Trials Office (TCI CCTO). In collaboration with the Executive Director , clinical trials investigators, and TCI CCTO Administration; this candidate is… more
- MTA (New York, NY)
- …Jan 9, 2025 Description Job Title: Principal Data Architect Reports To: Sr Director , Enterprise Information & Data Architecture Salary Range: $162,323 - $191,594 Hay ... data governance policies and frameworks to ensure data integrity, security, and compliance . + Lead data migration projects, ensuring minimal disruption and high data… more
