- Daiichi Sankyo, Inc. (Bernards, NJ)
- …pharmaceutical therapies to improve standards of care and address diversified, unmet medical needs of people globally by leveraging our world-class science and ... leadership and guidance as the lead statistician dedicated to safety on one or more safety monitoring...dedicated to safety on one or more safety monitoring team(s), accountable for all methodological and statistical… more
- Merck & Co. (Durham, NC)
- …a wide range of business activities.- Reporting directly to the Director , Supply Chain Management, the successful candidate's primary responsibilities will include ... the Master Data team with general Material Handling Steward tasksDrive safety , quality and process enhancements throughout the supply chain - Project… more
- Merck & Co. (Rahway, NJ)
- Job DescriptionAs a Technical Lead, you will report into Director , Chemical Technical Operations, External Manufacturing API Technology, and play a pivotal role in ... enhance performance.Maintain a strong focus on compliance and Environmental Health and Safety (EHS) to drive supply excellence.Serve as the primary technical contact… more
- Merck & Co. (Rahway, NJ)
- …facility in Rahway, New Jersey.The Sterile Process Engineer role at the Associate Director level will leverage the individual's leadership, technical, and ... change management.Familiarity with United States and European Union GMP and Safety compliance regulations.Ability to convert new drug product attributes and process… more
- Genmab (NJ)
- …love to have you join us!The Global Regulatory Labeling, Policy and Intelligence Associate Director will primarily be responsible for leading the development and ... will be within Global Regulatory Affairs (GRA) and will report to the Sr. Director , Labeling, Policy and Intelligence. The position may be based in our Princeton,… more
- Merck & Co. (Durham, NC)
- …Manufacturing Operations, Drug Delivery Systems and Devices within our Manufacturing Division ( Associate Director ).-This role serves as a Virtual Plant Manager - ... contact for all dealings between our Company and the External Partner, the Associate Director External Manufacturing Operations is accountable for establishing a… more
- Merck & Co. (Rahway, NJ)
- …and manufacturing to manage clinical development projects; and assist the Executive Director and/or Associate Vice President in ensuring that appropriate ... Job DescriptionThe Senior Director (Sr. Principal Scientist) has primary responsibility for...the clinical findings from studies to support decisions regarding safety and efficacy as well as new drug applications,… more
- Genmab (NJ)
- …feel like a fit? Then we would love to have you join us!The RoleThe 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
- Eisai, Inc (Exton, PA)
- …difference. If this is your profile, we want to hear from you. The Associate Director of Biologics Operations Upstream and Downstream is responsible for leading ... At Eisai, satisfying unmet medical needs and increasing the benefits healthcare provides...supporting technology transfer to external partners (as required). The Associate Director sets strategic directions and project… more
- Daiichi Sankyo, Inc. (Bernards, NJ)
- …pharmaceutical therapies to improve standards of care and address diversified, unmet medical needs of people globally by leveraging our world-class science and ... as R shiny apps for data surveillance, visualization, modeling and simulations, and safety signal detection. Lead the development and validations of R package and/or… more
- Eisai, Inc (Nutley, NJ)
- …If this is your profile, we want to hear from you. The Associate Director , Clinical Programming must have expertise in addressing technical challenges ... in SAS systems and application development and experience. The Associate Director must be a highly specialized...Safety Data Review and Clinical team. The Assoc. Director of Clinical Programming will oversee the Data Review… more
- Daiichi Sankyo, Inc. (Bernards, NJ)
- …pharmaceutical therapies to improve standards of care and address diversified, unmet medical needs of people globally by leveraging our world-class science and ... oversight groups for case processing activities and reports to the Director of PV Case Management.Responsibilities:ICSR Processing: Oversees QC activities, supports… more
- Merck & Co. (Rahway, NJ)
- …robust scientific methodology we collaborate to discover and develop the next medical breakthrough. Our Company's success is backed by ethical integrity, forward ... portfolio. Within Biologics and Biopharmaceutics, the large molecule product development Director will influence the strategy, lead activities, and develop a team… more
- Merck & Co. (Rahway, NJ)
- …support business objectives, with focus on Process Design and Process Safety for Small Molecule High Potency/Containment Projects. Develop project scope, front-end ... Participate in development and review of engineering guidelines, standards, safety /environmental policies, and change requests. Define intent in Front-End Loading,… more
- Merck & Co. (Rahway, NJ)
- …regulatory submissions.-Under the general scientific and administrative direction of the Director in Biologics Cell Culture Sciences group and working in conjunction ... projects as the leader of a cross-functional team.--Champion compliance and safety ; promote a culture of diversity, inclusion, and equity.Champion compliance and… more
- Merck & Co. (Durham, NC)
- …policies, procedures and business plan; receives guidance and oversight from Operations Associate Director and Director ;Interprets client and/or customer ... a team of individual contributor production direct reports including safety , quality, and daily operations;Ensure that Shift(s) objectives are...and any action plans to address gaps to the Associate Director and/or Director .- Identify,… more
- Eisai, Inc (Phoenix, AZ)
- …with internal cross functional partners including but not limited to Associate Director Regional Marketing, Oncology Field Reimbursement Managers, and ... At Eisai, satisfying unmet medical needs and increasing the benefits healthcare provides...Endocrinologists, and nurses, etc. learn about the efficacy and safety of Eisai's product(s) consistent with FDA approved label.… more
- BioSpace (Boston, MA)
- …is true to the best of my knowledge. Job Description About the role: The Associate Director , Clinical and Safety Quality Compliance is responsible for ... in partnership with functional compliance teams for regulations impacting Clinical, Safety and Clinical Pharmacovigilance Medical Quality (CPMQ) processes and… more
- Kailera Therapeutics, Inc. (Waltham, MA)
- …cultures, perspectives, and experiences to join our team. What You'll Do: The Associate Director , Clinical Data Management plays a key role within the ... As the primary data management representative on the study management team, the Associate Director coordinates ongoing DM activities, partnering closely with key… more
- Nuvalent, Inc. (Cambridge, MA)
- …Role: Reporting to the Senior Medical Director , Pharmacovigilance, the Associate Director , Drug Safety and Pharmacovigilance Scientist is responsible ... drug safety and pharmacovigilance regulations, pharmacovigilance practices, safety surveillance and risk-management practices. Responsibilities: *Provide medical… more
