- NVA (Yuma, AZ)
- …leading the decision-making process for medical protocols, staffing, manage associate veterinarians, assuring regulatory compliance, leadership development and ... Ironwood Veterinary Clinic, located in Yuma, AZ, is looking for aMedical Director / Managing Veterinarian to join our practiceIronwood Veterinary Clinic in Yuma,… more
- Eisai, Inc (Nutley, NJ)
- …make 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 & ... US monitoring activities, managing in-house efforts and third-party vendor engagements. The Associate Director will also play a critical role in advancing… more
- Merck & Co. (Boston, MA)
- …development strategy, study design, initiation, execution, monitoring, analysis, regulatory reporting, and publication.Specifically, the Senior Director ... and manufacturing to manage clinical development projects; and assist the Executive Director and/or Associate Vice President in ensuring that appropriate… more
- NVA (Ruskin, FL)
- …for the hospital ensuring quality care is provided, while also managing associate veterinarians, and assuring regulatory compliance. Alongside the Hospital ... and closed on Sundays Proud sponsor of Dr. Otts Dog ParkThe Opportunity: As the Medical Director at Ruskin Animal Hospital, you will provide medical leadership… more
- NVA (North Prairie, WI)
- …is given the authority to provide medical leadership for the hospital, manage Associate Veterinarians, lead and coach support staff, and ensure regulatory ... Pet Services and Insurance Future practice buy-in option Medical Director Leadership Qualities, Responsibilities:Advancing medical careLeading staff and practiceFinancial… more
- Merck & Co. (Rahway, NJ)
- …areas and routes of administration, including inhalation, implantation, and injection.The Associate Principal Scientist will lead the definition and execution of ... Company and with external partners.Author and review relevant portions of the regulatory submissions (INDs, IMPDs, NDAs, BLAs, etc.) for combination product programs… more
- Merck & Co. (Rahway, NJ)
- Job DescriptionJob Summary: -The Associate Director of Device Technology is a key leadership role within the Device Development and Technology Organization. This ... with a focus on autoinjectors, prefilled syringes, and other drug delivery systems. The associate director will be a technical subject matter expert on the… more
- Insmed Incorporated (San Diego, CA)
- …for Women™, Best Workplaces for Millennials™, and Best Medium Workplaces™ lists.OverviewThe Associate Director , EDC Programming will lead and oversee EDC ... the Biometrics teams, Clinical Operations teams, Clinical Development teams, Regulatory Affairs, and external partners.ResponsibilitiesEDC System Design & Development:Lead… more
- Lupin Pharmaceuticals (Coral Springs, FL)
- …profile (TPP) development, due diligence projects, and clinical- regulatory compliance. ResponsibilitiesEssential Duties and Responsibilities Clinical Development: ... execute clinical trials for respiratory products, ensuring compliance with regulatory requirements.Collaborate with cross-functional teams to develop study protocols,… more
- Merck & Co. (North Wales, PA)
- …in medical/legal/ compliance (CRT) reviews-Understanding of the US and Global regulatory stages and requirements-Job Owner - Fully responsible for asset management ... from creating job in PromoMats through AFD.-Lead discussion and negotiation, as appropriate, for each job during the live PRT review-Collaborate with agencies to prepare jobs for review, enhance, correct, and assure on strategy-Responsible to schedule,… 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 ... processes across the global safety organization. The incumbent will ensure regulatory compliance, promote best practices, foster a culture of continuous improvement… more
- Merck & Co. (Rahway, NJ)
- …and campus planning?- Have you advised on design standards, project scope, and regulatory compliance as well as act as a liaison with internal department ... building design standards, open space and site planning guidelines, and regulatory compliance such as ADA, environmental, and building codes.Ensure quality control… more
- Merck & Co. (Rahway, NJ)
- …into the Director , Logistics and Distribution Technology the Associate Director , Logistics and Distribution Technology will be responsible ... skills to shape the technical capabilities lead a global, cross-modality technical team.The Associate Director will lead a team of technical experts responsible… more
- Merck & Co. (North Wales, PA)
- …compliant supply of commercialized products for the benefit of patients. The Associate Director of Equipment Engineering is integral to this mission. ... issues.Strong knowledge of cGMP, FDA, EMA, and other international regulatory requirements.Strong analytical and decision-making abilities, combined with outstanding… 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
- 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
- Genmab (NJ)
- …to have you join us!The Global Regulatory Labeling, Policy and Intelligence Associate Director will primarily be responsible for leading the development and ... The lead may also be responsible for supporting various regulatory policy and/or intelligence deliverables. This role will be... Affairs (GRA) and will report to the Sr. Director , Labeling, Policy and Intelligence. The position may be… more
- Eisai, Inc (Nutley, NJ)
- …make a difference. If this is your profile, we want to hear from you. Associate Director , Medical Education - Oncology, is responsible for the strategic planning ... & ManagementEisai Salary Transparency Language:The base salary range for the Associate Director , Medical Education - Oncology is from :162,600-213,400Under… more
- Daiichi Sankyo, Inc. (Bernards, NJ)
- …timely deployment of CDx assays that are compliant with applicable global regulatory guidelines. Collaborates wtih Regulatory Affairs to develop CDx submission ... for the drug trials or for approval of CDx. Keeps abreast of regulatory and policy updates in the external environment and understands the competitive landscape.… more
- Daiichi Sankyo, Inc. (Bernards, NJ)
- …research areas centered around rare diseases and immune disorders. SummaryThe Senior Director of Clinical Operations will manage clinical operations staff to ensure ... ongoing collaboration and communication with internal stakeholders. Detailing The Senior Director will ensure a robust communication plan including status and timing… more
