- Merck & Co. (North Wales, PA)
- Job DescriptionThe Associate Director of Data Operations Management plays a pivotal role in driving enterprise-wide data governance, access provisioning, and ... is responsible for ensuring data integrity, accessibility, and compliance with regulatory standards, while also enabling business users to derive actionable insights… more
- Merck & Co. (North Wales, PA)
- … Regulations , IT Coordination, IT Operation, Pharmacovigilance, Policy Implementation, Regulatory Compliance, Regulatory Labeling, Regulatory Operations, ... Source Management Business Operations Lead is expected to understand the end-to-end regulatory submission process. The main focus will be on document production… more
- Merck & Co. (Millsboro, DE)
- …operations, formulation and fill/finish activities.Ensure compliance with corporate and regulatory requirements (cGMP/USDA) and lead IPT support for audits, ... Quality Notifications and technical documentation; collaborate cross-functionally with QA, Regulatory Affairs, EHS, Engineering, BTS, ATS and HR.Direct technical… more
- Daiichi Sankyo, Inc. (Bernards, NJ)
- …primarily focused on providing novel therapies in oncology, as well as other research areas centered around rare diseases and immune disorders. Job Summary: This 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 daily… more
- Merck & Co. (Rahway, NJ)
- Job DescriptionThe Associate Director, Engineering, Packaging Commercialization will lead packaging development for new products including parenteral products ... erience developing and commercializing new products on cross-functional teams. - - The Associate Director will be accountable for the d efinition and execution of… more
- Eisai, Inc (Nutley, NJ)
- …is breaking through in neurology and oncology, with a strong emphasis on research and development. Our history includes the development of many innovative medicines, ... a difference. If this is your profile, we want to hear from you. The Associate Director, Compliance Operations will be a key member of Eisai's US Ethics & Compliance… more
- Merck & Co. (Rahway, NJ)
- …DescriptionReporting into the Director, Logistics and Distribution Technology the Associate Director, Logistics and Distribution Technology will be responsible and ... to shape the technical capabilities lead a global, cross-modality technical team.The Associate Director will lead a team of technical experts responsible providing… more
- Merck & Co. (Millsboro, DE)
- …a safe working environment in compliance with local, state, and federal regulations . The Sr. Specalist of Biosafety will collaborate with various departments to ... the Global Safety & Environment organization, and reports to the Associate Director of Safety & Environment at Millsboro, DE.Responsibilities:Ensure compliance with… 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 for a ... Capital Procurement Project Execution within the Global Capital Procurement organization, the Associate Director will serve as the primary point of contact for… more
- Merck & Co. (Rahway, NJ)
- …platforms ensuring internal technical requirements are achieved and ensure filings with regulatory bodies to ensure compliance with relevant regulations and ... DescriptionReporting into the Director Packaging Platform Technical Leadership the Associate Director Medical Device and Combination Product (MDCP) Platform… more
- Eisai, Inc (Pittsburgh, PA)
- …is breaking through in neurology and oncology, with a strong emphasis on research and development. Our history includes the development of many innovative medicines, ... with internal cross functional partners including but not limited to Associate Director Regional Marketing, Oncology Field Reimbursement Managers, and other… more
- JENAVALVE TECHNOLOGY INC (Irvine, CA)
- …Title: Senior Manager, Clinical Affairs Job Description Summary: The Senior Clinical Research Associate will report to the Associate Director, ... the conduct of pre-market clinical studies and ensure compliance with all regulatory requirements. The ideal candidate will have a thorough knowledge of Good… more
- UNC Health (Chapel Hill, NC)
- …or HIM.Knowledge/Skills/and Abilities Requirements:* Advanced and demonstrated ability to research regulations and understand professional billing and ... processes, documents and reports, and ensuring compliance with internal and external regulatory framework. Serves as an expert resource to physicians, coders and… more
- Protagonist Therapeutics (Newark, CA)
- …in both the US and global markets, knowledge of relevant FDA and EMA regulations and able to work within regulatory agency requirements. Strategic thinker and ... Associate Director, API Development Protagonist Therapeutics is seeking...Development Protagonist Therapeutics is seeking an experienced API process research and development chemist to support route scouting, organic… more
- DERMCARE MANAGEMENT LLC (Hollywood, FL)
- …research participants to ensure adherence to study rules. Adhering to research regulatory standards. Adhering to ethical standards. Maintaining detailed ... Hollywood - Hollywood, FL Travel Percentage Negligible Job Shift Day Job Category Research Description Clinical Research Coordinator Compnay Name: Skin Center … more
- InTandem HR (Denver, CO)
- …and payment tracking for benefit providers, taxing entities, and other vendors. Research variances in accounting ledgers and other reports as requested by management ... Accounting teams Compliance and Documentation: Ensure compliance with relevant regulations and company policies regarding employee benefits accounting. Maintain… more
- UTMB Health (Galveston, TX)
- Regulatory Associate ( Research , Regulations and Compliance - Galveston) **Galveston, Texas, United States** **New** Research Academic & Clinical UTMB ... requirements. + Works under limited supervision to assure compliance with federal regulations relating to human subject research . + Works under limited… more
- Rush University Medical Center (Chicago, IL)
- …as a Certified Clinical Research Professionals (CCRP), Certified Clinical Research Associate (CCRA), Certified Clinical Research Coordinator (CCRC), ... veteran status, and other legally protected characteristics. **Position** Clinical Research Regulatory Coordinator **Location** US:IL:Chicago **Req ID** 21135 more
- Stanford University (Stanford, CA)
- Cancer Clinical Research Coordinator Associate - GI (Hybrid) **School of Medicine, Stanford, California, United States** Research Post Date Sep 23, 2025 ... Requisition # 106962 **Cancer Clinical Research Coordinator Associate - GI Oncology** The...scheduling. **Duties include*:** + Serve as primary contact with research participants, sponsors, and regulatory agencies. Coordinate… more
- Stanford University (Stanford, CA)
- Clinical Research Coordinator Associate **School of Medicine, Stanford, California, United States** Research Post Date Jun 10, 2025 Requisition # 106623 The ... Clinical Research Coordinator Associate is responsible for the...management and implementation of an assigned set of multiple research protocols assuring efficiency and regulatory compliance.… more
