- Merck & Co. (North Wales, PA)
- …Owner for one or more of the QMS processes managed under GRACS(Global Regulatory Affairs & Clinical Safety ) Quality &Compliance.Establishes and maintains an ... Regulatory Practice, Good Pharmacovigilance Practice, Good Clinical Practice,), safety guidelines and company policies and procedures.-May assist with the… more
- Merck & Co. (Durham, NC)
- …Description Position Description: Under the direction of the Network Strategy & Execution Director , the Associate Director is responsible for assessing, ... teams to ensure delivery of the targeted goals and timelines. The Associate Director will effectively and efficiently achieve project objectives and… more
- Daiichi Sankyo, Inc. (Bernards, NJ)
- …is a global role that will cover signal activity across all DS regions. The Associate Director of the Signal Management Center of Excellence (CoE) will lead the ... optimize, and innovate signal detection and management processes across the global safety organization. The incumbent will ensure regulatory compliance, promote… more
- Genmab (NJ)
- …and feel like a fit? Then we would love to have you join us!Role:The Associate Director acts as a statistical expert supporting the clinical development of ... as trial responsible statistician with responsibilities as described below. The Associate Director contributes to clinical development strategies and… more
- Lupin Pharmaceuticals (Coral Springs, FL)
- …desired product characteristics such as indications, target population, dosing regimen, safety profile, and clinical efficacy.Align TPPs with regulatory ... target product profile (TPP) development, due diligence projects, and clinical- regulatory compliance. ResponsibilitiesEssential Duties and Responsibilities Clinical Development: Design… more
- Merck & Co. (Millsboro, DE)
- …for IPT performance against site and division goals, including quality, safety , delivery, cost of goods, and budget forecasts.Translate site strategy into ... operations, formulation and fill/finish activities.Ensure compliance with corporate and regulatory requirements (cGMP/USDA) and lead IPT support for audits,… more
- Merck & Co. (Upper Gwynedd, PA)
- …science that radically changes the way we approach serious diseases. --The Senior Director will report to an Associate Vice President in the Oncology ... Clinical Research Group. Under the guidance of a supervisor, the Senior Director has primary responsibility for the planning and directing of clinical research… more
- Merck & Co. (Rahway, NJ)
- …DescriptionReporting into the Director Packaging Platform Technical Leadership the Associate Director Medical Device and Combination Product (MDCP) Platform ... compliant supply of commercialized products for the benefit of patients. The Associate Director of MDCP Platform Packaging and Assembly Technical Leadership… more
- Merck & Co. (Rahway, NJ)
- Job Description Role Summary The Associate Director of Procurement for Capital Projects will be responsible for overseeing and managing procurement activities ... of Capital Procurement Project Execution within the Global Capital Procurement organization, the Associate Director will serve as the primary point of contact… more
- Merck & Co. (Millsboro, DE)
- …the Global Safety & Environment organization, and reports to the Associate Director of Safety & Environment at Millsboro, DE.Responsibilities:Ensure ... Biosafety, EHS Auditing, EHS Compliance, EHS Program Management, Environmental Regulatory Compliance, Health and Safety Legislation, Incident Investigations,… more
- Eisai, Inc (Pittsburgh, PA)
- …with internal cross functional partners including but not limited to Associate Director Regional Marketing, Oncology Field Reimbursement Managers, and ... Hematologists, Endocrinologists, and nurses, etc. learn about the efficacy and safety of Eisai's product(s) consistent with FDA approved label. Works with… more
- IQVIA (Durham, NC)
- ** Associate Director , Data Sciences, Safety , and Regulatory FSP Sales** Associate Director , Data Sciences, Safety , and Regulatory , FSP ... - FSP services for the Data Management, Biostatistics, Programming, Medical Writing, Lifecycle Safety , and Regulatory Affairs functions - and will be responsible… more
- BeOne Medicines (San Mateo, CA)
- We seek an experienced professional to lead our Safety and Regulatory Analytics initiatives. This role is responsible for transforming data into actionable ... stakeholders. **General Description:** We seek an experienced professional to lead our Safety and Regulatory Analytics initiatives. This role is responsible for… more
- Takeda Pharmaceuticals (Boston, MA)
- …is possible in order to bring life-changing therapies to patients worldwide. The Associate Director , Global Regulatory Affairs Advertising and Promotion (GRA ... pertaining to prescription medicine promotion. **How you will contribute:** + As our Associate Director , Global Regulatory Affairs Advertising and Promotion… more
- TXNM Energy (Albuquerque, NM)
- Associate Director , Grid Modernization (PM, Regulatory & Accounting) Location: Albuquerque, NM, United States Job ID: 6089242 Date Posted:Sep 5, 2025 **JOB ... DESCRIPTION** Associate Dir, Grid Modernization Salary Grade: G03 Minimum Midpoint...regulatory mandates, fostering public trust and organizational growth ** SAFETY AND ADA STATEMENT** Safety Statement: … more
- Kemin Industries (Des Moines, IA)
- Overview Kemin Health is hiring an Associate Director of Regulatory /Scientific Affairs and Quality! In this role, you will be responsible for leading the ... at state, national, and international levels. They will monitor and influence regulatory changes, support product safety , substantiate claims, and ensure label… more
- CSL Behring (King Of Prussia, PA)
- …therapies that make a meaningful difference worldwide. Could you be our next Associate Director Global Regulatory Lead, EHT (Enabling Healthcare Technologies ... and is onsite three days a week. You will report to the Executive Director Head Regulatory . **Position Description** **Summary** * Regulatory leaders who… more
- Gilead Sciences, Inc. (Foster City, CA)
- …others in accomplishing Corporate Objectives. + Responsible for submitting complex regulatory documents including safety reports, amendments, supplements and ... Sheets (CCDS) for assigned products. + Contributes to the regulatory review of draft Product Company Core Safety... regulatory review of draft Product Company Core Safety Information (CCSI) and ensures updates to the CCDS… more
- UTMB Health (Galveston, TX)
- Associate Director of Quality Management & Patient Safety **Galveston, Texas, United States** Executive - Nursing & Patient Care UTMB Health Requisition # ... 2502806 **Job Summary:** The Associate Director of Quality Management & Patient Safety ...and health system activities, including federal, state, and local regulatory compliance across the UTMB network of hospitals and… more
- Merck (Rahway, NJ)
- …Owner for one or more of the QMS processes managed under GRACS(Global Regulatory Affairs & Clinical Safety ) Quality &Compliance. + Establishes and maintains ... Good Regulatory Practice, Good Pharmacovigilance Practice, Good Clinical Practice,), safety guidelines and company policies and procedures. + May assist with the… more
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