- Merck & Co. (North Wales, PA)
- …with applicable and established Standard Operating Procedures (SOPs), applicable regulations (eg, Good Regulatory Practice, Good Pharmacovigilance Practice, ... to achieve quality goals and understanding of and application of appropriate regulations in partneringwith our Research & Development Division area.May develop,… more
- 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
- 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
- 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)
- 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
- Merck & Co. (Rahway, NJ)
- Job Description Position Description: As a member of the Company's Research Laboratories Quality Assurance community, provide for and lead Quality Assurance ... matters within the Global Development Quality organization and for the Company's Research & Development division.For our Company Clinical Supply, act as the Quality… 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)
- …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
- Merck & Co. (Rahway, NJ)
- …education activities supporting the monitoring roles in clinical operations eg -Clinical Research Associate (CRAs), Clinical Research Managers (CRMs), -in ... Required -Experience: - 5 years of experience in clinical research , with mandatory 2 years of CRA experience. -...FDA Good Clinical Practices, ICH Guidelines, and other major regulatory agencies' regulations and guidance. - Experience… 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
- Daiichi Sankyo, Inc. (Bernards, NJ)
- …focused on providing novel therapies in oncology, as well as other research areas centered around rare diseases and immune disorders. SummaryThe Senior Director ... Clinical Practices (GCPs), appropriate Standard Operating Procedures (SOPs) and relevant regulations Food and Drug Administration (FDA) regulations /EU Directive,… 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)
- …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
- 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
- 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
- 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
- University of Pennsylvania (Philadelphia, PA)
- …policies as well as all applicable regulatory bodies and guidelines. The Associate Director will lead research teams, manage resources, and guide the ... programs and resources, and much more. Posted Job Title Associate Director C, Research Job Profile Title...of Harmonization (ICH) Guidelines. Knowledge of IRB and human research protection regulations . + Supervisory experience and/or… 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
