- Daiichi Sankyo, Inc. (Bernards, NJ)
- …timelines.Develop quality systems and procedures for the signaling activities to assure regulatory compliance and meet regulatory reporting timelines. ... 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
- Insmed Incorporated (San Diego, CA)
- …Women™, Best Workplaces for Millennials™, and Best Medium Workplaces™ lists.OverviewThe Associate Director, EDC Programming will lead and oversee EDC programming, ... the Biometrics teams, Clinical Operations teams, Clinical Development teams, Regulatory Affairs, and external partners.ResponsibilitiesEDC System Design & Development:Lead… more
- Eisai, Inc (Nutley, NJ)
- …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 ... US monitoring activities, managing in-house efforts and third-party vendor engagements. The Associate Director will also play a critical role in advancing the… more
- Merck & Co. (North Wales, PA)
- …drug/vaccine clinical development projects.Develop and execute statistical analysis and reporting deliverables (eg safety and efficacy analysis datasets, tables, ... span of which range from individual clinical trials to world-wide regulatory application submissions and post marketing support.-Design and maintain statistical… more
- Merck & Co. (Rahway, NJ)
- …process validation, second generation process development and authoring of regulatory submissions.-Under the general scientific and administrative direction of the ... next generation process development and characterization, process validation, and regulatory submission authoringIn this role, the successful candidate will be… more
- Merck & Co. (Upper Gwynedd, PA)
- Job DescriptionThe Associate Director within Metrics, Analytics & Performance (MAP) has experience in clinical operations and is responsible for leading the ... business questions for GCTOManaging project timelines to enable accurate reporting and functionality during SDLCManaging diverse projects and processes within… more
- Merck & Co. (North Wales, PA)
- …art scientific methodologies and tools to enable the discovery, development, regulatory approval, manufacturing, and marketing of medical drugs and vaccines for ... predominantly includes the development and execution of statistical analysis and reporting deliverables (eg safety and efficacy analysis datasets, tables, listings,… more
- Legend Biotech USA, Inc. (Raritan, NJ)
- …an immunotherapy in the treatment of multiple myeloma.Legend Biotech is seeking an Associate MES Engineer as part of the Manufacturing Excellence team based in ... Raritan, NJ. Role OverviewThe Associate MES Engineer will be part of MSAT team reporting to the Manufacturing Execution Systems Lead and will be responsible for… more
- Merck & Co. (North Wales, PA)
- Job DescriptionThe Associate Vice President (AVP)/Section Head, Global Clinical Development, Pediatrics will focus on driving strategy, development, and life-cycle ... the external community (Key Scientific Leaders, Patient Community, Payers, Regulatory Agencies)Responsible for managing, coaching, and mentoring Clinical Directors… more
- Eisai, Inc (Nutley, NJ)
- …a difference. If this is your profile, we want to hear from you. Associate Director, Medical Education - Oncology, is responsible for the strategic planning and ... input into CME budget and website portal as needed. Ensure compliance with regulatory and other ethical guidelines relevant to the pharmaceutical industry, and to… more
- Vantive (Oakdale, MN)
- …research and development projects for new and existing products. The Research Associate III, Stability Subject Matter Expert, applies sound chemistry and stability ... and makes recommendations that are non-routine to address technical, regulatory , and business requirements.WHAT YOU WILL BE DOINGRepresent R&D-Stability on… more
- NVA (Yuma, AZ)
- …leading the decision-making process for medical protocols, staffing, manage associate veterinarians, assuring regulatory compliance, leadership development and ... is supported by their AZ Divisional Leadership who provides practice management training, reporting , and ongoing resources to develop a best in class hospital. The… more
- NVA (Sulphur, LA)
- …is primarily responsible for providing medical leadership for the hospital, managing associate veterinarians, and assuring regulatory compliance relating to the ... by their Louisiana-based Divisional Leadership who provides practice management training, reporting , and ongoing resources to develop a best in class hospital.… more
- Daiichi Sankyo, Inc. (Bernards, NJ)
- …operational aspects of clinical study planning, implementation, data delivery and reporting . Will represent DSPD Clinical Operations in a range of cross-functional ... program. This position will require line management responsibility of Directors, Associate Directors, Clinical Study Managers, who are primarily responsibility for… more
- Merck & Co. (Boston, MA)
- …medicine leader in our newly created Precision Medicine and Diagnostics function. Reporting to the Associate Vice President ,Precision Medicine and Diagnostics, ... of biomarkers/diagnostics arising from these. Key Responsibilities Work with the Associate Vice President Precision Medicine and Diagnostics/TA Vice President and… more
- Merck & Co. (Millsboro, DE)
- …actions to prevent recurrence.Maintain records of incidents and ensure proper reporting to relevant regulatory authorities as required.Conduct regular ... 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)
- …development strategy, study design, initiation, execution, monitoring, analysis, regulatory reporting , and publication.Specifically, the Senior Director ... closely with a cross-functional group of experts in commercialization, regulatory affairs, statistics, and manufacturing to manage clinical development projects;… more
- Eisai, Inc (Dayton, OH)
- …and Reimbursement team under Patient Services/Market Access. Working closely with and reporting to the Associate Director, Access and Reimbursement, the ARM, ... Cross-functional Influence, Critical Thinking & Business Agility, Industry & Regulatory (Market Access), Mentoring/ People Development, Project Management, Reimbursement… more
- Ochsner Health (Gretna, LA)
- …within their span of control.EducationRequired - Registered nurse diploma.Preferred - Associate or bachelor's degree in nursing.ExperienceRequired - 1 year of ... of operational success such as unit productivity, expense management, regulatory requirements, and quality indicators.Proficiency in using computers, software, and… more
- Eisai, Inc (Nutley, NJ)
- …is a Commercial Training and Development role that will report into the Associate Director, Field Training, and will have strong collaboration and relationships with ... new hires by providing initial training on sales performance and call reporting platforms.Serves as Subject Matter Expert for advanced trainings by assisting… more
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