- Merck & Co. (Rahway, NJ)
- …(Sr. Principal Scientist) has primary responsibility for the planning and directing clinical research activities involving new or marketed Oncology medicines. ... study reports, or publication; andParticipation in internal and joint internal/external research project teams relevant to the development of new compounds,… more
- Merck & Co. (Rahway, NJ)
- …(Principal Scientist) has primary responsibility for the planning and directing of clinical research activities involving new or marketed Oncology medicines. Our ... study reports, or publication; andParticipation in internal and joint internal/external research project teams relevant to the development of new compounds,… more
- Novo Nordisk Inc. (Plainsboro, NJ)
- …experience as a Clinical Trial/ Project Manager Experience with global clinical trial operations, in multiple phases of research Strong knowledge of ICH ... MA and Plainsboro, NJ. We support programs from early research through late-stage clinical development. We are...difference? The Position We are looking to hire a Clinical Project Manager (CPM). This is a… more
- Genmab (Plainsboro, NJ)
- …development strategy. Works in collaboration with a Medical Director and Sr. level Clinical Research Scientist as indicated for ongoing clinical ... in collaboration with a Medical Director and Sr. level Clinical Research ScientistAssists to execute the ...of a trial protocol and to other study-related and regulatory documentsAssists in the development of case report forms… more
- Daiichi Sankyo, Inc. (Bernards, NJ)
- …throughout the product's lifecycle and across different indications. Represent Global Regulatory Affairs on the GPT (Global Project Team), Daiichi ... corporate goals, and regional regulatory requirements/precedence.Represent Daiichi Sankyo's regulatory group in internal and external development project … more
- Novo Nordisk Inc. (Plainsboro, NJ)
- …facilities in Lexington, MA and Plainsboro, NJ. We support programs from early research through late-stage clinical development. We are building for the future, ... and associated mitigation plans to management and other internal stakeholders Perform regulatory review of all clinical and nonclinical documents for… more
- Merck & Co. (Rahway, NJ)
- … trial material and in support of product and process development. Project management skills Established scientific or regulatory reputation supported by ... Job DescriptionThe Small Molecule Analytical Research and Development (SMAR&D) group has an exciting...methodologies to characterize and release raw materials, package components, clinical drug substance, and clinical drug product… more
- Merck & Co. (Rahway, NJ)
- …and key strategic engagements. This includes the ability to:Apply strong knowledge of clinical research regulatory requirements (eg, GCP and ICH)Manage ... on the clinical trial team.Collaborates with the Medical Writer on clinical /scientific and regulatory documents. Partners with Study Manager on study… more
- Daiichi Sankyo, Inc. (Bernards, NJ)
- …Complies with the protocol, Policies, SOPs, external/internal standards, pertinent Good Clinical Practices (GCPs), applicable regulatory requirements, and other ... primarily focused on providing novel therapies in oncology, as well as other research areas centered around rare diseases and immune disorders. Summary The Manager, … more
- Merck & Co. (Rahway, NJ)
- …and manage scientific activities on clinical protocols.Apply strong knowledge of clinical research regulatory requirements (eg, GCP and ICH)Manage ... the clinical trial team.Collaborates with the Medical Writer on clinical /scientific and regulatory documents.Partners with Study Manager on study… more
