- Genmab (NJ)
- …biological, pharmaceutical science or related discipline Minimum of 8 years of experience in clinical research with at least 4 or more years of drug development ... implementation of the global development strategy leading or co-leading one or more clinical trials in a therapeutic area for one or more compounds in various… more
- Merck & Co. (Rahway, NJ)
- … Clinical Development, has primary responsibility for the planning and directing clinical research activities involving new or marketed drugs in the Oncology ... Clinical Research group and in the field...clinical studies.--Will report and work collaboratively with the- Associate Vice President to promote the development strategy of… more
- Merck & Co. (Rahway, NJ)
- …Scientist) has primary responsibility for the strategic planning and directing clinical research activities involving investigational compounds in Immunology. ... about twenty (20) percent of the time to manage future or ongoing clinical research projects.EducationM.D. or, DO-Required education and experience-Minimum of 5… more
- Merck & Co. (Rahway, NJ)
- …role involves close collaboration with numerous stakeholders such as , Clinical Research Associates, Statisticians, Quality Assurance, and Regulatory Affairs ... to drive data excellence and enhance the efficiency of our clinical research operations.Key Responsibilities:- Lead Data Management Initiatives:-Direct the… more
- Merck & Co. (Rahway, NJ)
- Job DescriptionOur Research Scientists are our Inventors.- Using innovative thinking, state-of-the-art facilities, and robust scientific methodology, we partner to ... deliver the next medical breakthrough.Biologics Process Research & Development (BPR&D) within our company's Research Laboratories is on a mission to rapidly… more
- Aequor (South San Francisco, CA)
- Job Title : Research Associate II Location : South San Francisco, CA Duration : Until 01/12/2026 Job Description: The mission of the Investigative Toxicology ... toxicities that are observed non-clinically and / or in clinical trials through hypothesis driven research . This...or in clinical trials through hypothesis driven research . This process involves closely collaborating with scientists across… more
- Genmab (NJ)
- …to the effective planning, and timely delivery of complete, high quality and reliable clinical trial data. The Associate Director DM will provide oversight to ... be our best, and authentic is essential to fulfilling our purpose.The Role:An Associate Director, Data Management is operationally responsible for the oversight of … more
- Merck & Co. (Rahway, NJ)
- …Clinical Supply organization is accountable for managing the 'end-to-end' integrated clinical supply chain across the full company Research Laboratories ... portfolio of clinical trials.- Global Clinical Supply is accountable for the planning, sourcing, labeling, packaging and delivery of clinical supplies to … 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. Summary This position ... works with the Director, Clinical Study Startup to establish... Study Startup to establish the strategy driving global Clinical Study Start-Up activities for PV Safety Operations. This… 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. Summary Oversees typically ... trial (small size, standard complexity in design and geographic scope). Prepares clinical section of regulatory document. Collaborates as team member with AROs/CROs.… more
- Genmab (Plainsboro, NJ)
- …our best, and authentic is essential to fulfilling our purpose.The RoleThe Global Clinical Trial Manager (GCTM) is accountable for the end-to-end delivery of a ... single or multiple clinical trials from strategy outline through to CSR by...has invented next-generation antibody technology platforms and leveraged translational research and data sciences, which has resulted in a… more
- Merck & Co. (Rahway, NJ)
- …--The Director will report to an Associate Vice President in the Oncology Clinical Research Group. Under the guidance of a supervisor, the Director has ... primary responsibility for the planning and directing of clinical research activities involving new or marketed Oncology medicines. Our Oncology medicines span… more
- Merck & Co. (Rahway, NJ)
- …& Respiratory Therapeutic Area and strategy, bridging the continuum from Discovery Research through Late-Stage Clinical Development.- The AVP provides strategic ... Job DescriptionThe Associate Vice President (AVP) will be responsible for...and tactical role in overseeing the scientific direction of clinical programs involving translational research and early… more
- Daiichi Sankyo, Inc. (Bernards, NJ)
- … clinical studies, under the supervision of the Study Manager role the Study Associate Manager within Clinical Operations, in adherence to the protocol, Good ... or More Years with Bachelor of Science required- Experience considered relevant includes clinical or basic research in a Pharmaceutical company, a Medical… more
- Merck & Co. (Rahway, NJ)
- Job DescriptionPosition Description: Associate Principal Statistical Programmer - Oncology (Hybrid) In BARDS (Biostatistics and Research Decision Sciences), a ... distinguished department within our Company's renowned Research and Development division, quantitative scientists, in partnership with other subject matter experts,… more
- Merck & Co. (North Wales, PA)
- Job DescriptionRole SummaryThe Oncology Regional Medical Scientific Director ( Associate RMSD) is a credentialed (ie, PhD, PharmD, DNP, MD) therapeutic and disease ... products. The work of an RMSD is aligned to: Scientific Exchange, Research , Scientific Congress Support, and Scientific Insights.RMSDs liaise between the scientific… more
- Merck & Co. (Rahway, NJ)
- …Quantitative Pharmacology and Pharmacometrics - Immune/Oncology (QP2-IO) team in the role of Associate Director QP2-IO team is part of the Global Clinical ... organization and has oversight over drug development aspects related to clinical pharmacology and pharmacometrics of oncology drugs from post-PCC to registration.… more
- Merck & Co. (Rahway, NJ)
- Job Description Job Description: The Biologics Process Research & Development organization within our company's Research Laboratories is responsible for ... company's biologics pipeline. We work closely with colleagues in Discovery, Pre- clinical and Early Development to rapidly develop manufacturing processes for diverse… more
- Merck & Co. (Rahway, NJ)
- Job DescriptionThe Biologics Process Research & Development organization within our company's Research Laboratories is responsible for developing the drug ... company's biologics pipeline. We work closely with colleagues in Discovery, Pre- clinical and Early Development to rapidly develop manufacturing processes for diverse… 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. Summary The ... Associate Director of Regulatory Writing is a key role...a key role responsible for producing scientifically accurate, high-quality clinical regulatory documents while adhering to regulatory guidelines. This… more
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