- Eisai, Inc (Nutley, NJ)
- …a difference. If this is your profile, we want to hear from you. The Associate Director (AD), Global Medical Affairs Training and Education is responsible ... mentoring MSLs to assist with their onboarding and continued development . In addition, the position will support global...Eisai Salary Transparency Language:The base salary range for the Associate Director , Global Medical Affairs… more
- Merck & Co. (Rahway, NJ)
- Job DescriptionDevice Development Associate Principal Scientist - Development Strategy, Design Controls( Associate Director Equivalent) Our company's ... device development or design controls areaKnowledge of US and global medical device and healthcare regulations, including FDA combination products cGMP, Quality… more
- Daiichi Sankyo, Inc. (Bernards, NJ)
- … Global Regulatory Strategy in the Drug and Device Development and Commercialization process.Experience with developing and documenting regulatory strategies in ... for cardiovascular diseases, under the Group's 2025 Vision to become a " Global Pharma Innovator with Competitive Advantage in Oncology," Daiichi Sankyo is primarily… more
- Genmab (NJ)
- …and/or as trial responsible statistician with responsibilities as described below. The Associate Director contributes to clinical development strategies and ... diseases. We strive to create, champion and maintain a global workplace where individuals' unique contributions are valued and...Then we would love to have you join us!Role:The Associate Director acts as a statistical expert… more
- Merck & Co. (Rahway, NJ)
- …a strong, integrated understanding of the strategic elements of drug discovery and development . The Associate Director should demonstrate collaborative work ... / Rahway, NJ is seeking a curious and collaborative Associate Director to support our rapidly expanding...e ntis ts to discover and advance the clinical development of novel therapeutic agents for cardiometabolic and ophthalmologic… 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 ... Regulatory Affairs (GRA) and will report to the Sr. Director , Labeling, Policy and Intelligence. The position may be...labeling subject matter expert responsible for advising teams on global labeling strategies based on Genmab's development … more
- Merck & Co. (Rahway, NJ)
- …component of decision-making at our Company, this position offers an opportunity for the Associate Director to drive pipeline impact across therapy areas. - This ... and Pharmacometrics (QP2) department drive model-informed drug discovery and development (MIDD) to routinely enable efficient drug discovery/ development... Associate Director will work with scientists within… more
- Merck & Co. (Rahway, NJ)
- Job DescriptionAssociate Director , Business System Labeling Management Required experience and skills: Min. 5-10 years of experience with Pharmaceutical Regulatory ... IT or related discipline with functional working experience in System Development /Management within Manufacturing or Research areas preferred.Start date: -As soon as… more
- Merck & Co. (Rahway, NJ)
- …of the probability of regulatory success together with risk mitigation measures.-Lead development and execution of global product and project regulatory ... Job DescriptionGRACS CMC - Associate Principal Scientist, CMC, R4 - Pharm Pre-approval...CMC, R4 - Pharm Pre-approval Reporting to the Sr Director / Director /Principal Scientist/Sr Principal Scientist in Pre-approval Pharmaceutical… more
- Merck & Co. (Rahway, NJ)
- Job DescriptionRole SummaryUnder the guidance of a senior leader, an Associate Principal Scientist/ Associate Director , has primary responsibility for ... reviews and meta-analyses, and economic modelling. Key responsibilities also include development of American Managed Care Pharmacy (AMCP) dossiers for US payers,… more
