- Merck & Co. (Rahway, NJ)
- …Principal Scientist ) has primary responsibility for the planning and directing clinical research activities involving new or marketed Oncology medicines. Our ... about twenty (20) percent of the time to manage future or ongoing clinical research projects.Education:- MD or MD/Ph.D. or Ph.DRequired:Must have experience in… more
- Merck & Co. (Rahway, NJ)
- … Scientist )has primary responsibility for the planning and directing of clinical research activities involving new or marketed Oncology medicines. Our ... Certified or Eligible in Oncology (and/or Hematology)Prior specific experience in clinical research and prior publication is desirable but not… more
- Merck & Co. (Rahway, NJ)
- …imaging tools, and data analy sis. You would also contribute towards regulatory submissions to enable clinical trials. Your main responsibilities include: ... Job DescriptionThe Small Molecule Analytical Research and Development (SMAR&D) group has an exciting...(SMAR&D) group has an exciting opportunity for a Principal Scientist based in Rahway, NJ. Join us and experience… more
- Tris Pharma (Monmouth Junction, NJ)
- …Monmouth Junction, New Jersey, Tris Pharma has an immediate opening for a Clinical Scientist /Grant AdministratorSUMMARY:The Clinical Scientist supports ... aspects of the development, oversight and execution of phase I to IV clinical research trials. Collaborating closely with Physicians, Clinical Leaders… more
- Catalent (St. Petersburg, FL)
- Associate Scientist II, Analytical Research & Development Position Summary Catalent is a global, high-growth, public company, and a leading partner for the ... services to solve difficult development and manufacturing challenges. The Analytical Research and Development (AR&D) laboratory that supports evaluation and testing… more
- Merck & Co. (Rahway, NJ)
- …for a Principal Scientist position available at its Kenilworth, New Jersey research facility. The Principal Scientist is a senior scientific role tasked with ... Job DescriptionThe Biologics Analytical Research & Development department of our company's ...of release, characterization, and stability assays for testing of clinical trial material and in support of product and… more
- Daiichi Sankyo, Inc. (Basking Ridge, NJ)
- …trial (small size, standard complexity in design and geographic scope). Prepares clinical section of regulatory document. Collaborates as team member with ... focused on providing novel therapies in oncology, as well as other research areas centered around rare diseases and immune disorders. Summary Oversees typically… more
- Merck & Co. (North Wales, PA)
- …datasets, tables, listings, figures), the span of which range from individual clinical trials to world-wide regulatory application submissions and post marketing ... of statistical databases that support multiple stakeholder groups which include clinical development, outcomes research and safety evaluation.The position is… more
- Merck & Co. (Rahway, NJ)
- Job DescriptionAssociate Principal Scientist , Small Molecule Research & DevelopmentIn your role as Associate Principal Scientist , you will be part of a team ... imaging tools, and data analysis. You would also contribute towards regulatory submissions to enable clinical trials. Your main responsibilities,… more
- Merck & Co. (Rahway, NJ)
- …robust and scalable upstream processes for biologics in different stages of clinical development, 2) process characterization and regulatory filings for ... Job DescriptionPosition Description: Principal Scientist , Upstream Bio Process Development BPR&D within our..., Upstream Bio Process Development BPR&D within our Company's Research Laboratories is on a mission to rapidly deliver… more
- Merck & Co. (Rahway, NJ)
- …, Regulatory , Statistical Programming, Data Management, and our company's Research Laboratories Scientists in designing and analyzing clinical trials, and ... in coordinating the statistical activities for clinical drug/vaccine projects.Interacts with Academic Research Organization (ARO), Contract Research … more
- Merck & Co. (North Wales, PA)
- …drug/vaccine projects under supervision in Late Development Statistics. --Interacts with Clinical , Regulatory , Statistical Programming, Data Management and other ... of our company's Research Laboratories Scientists in designing and analyzing ...oral and written reports to effectively communicate results of clinical trials to the project team, management, regulatory… more
- Merck & Co. (North Wales, PA)
- …creation of the SDTM deliverables for analysis and reporting and world-wide regulatory application submissions of drug and vaccine clinical development projects. ... with internal and external stakeholders including Statistical Programming, Statistics, Regulatory , Data Management, Clinical and other project… more
- Merck & Co. (North Wales, PA)
- …position is a key collaborator with internal and external stakeholders including Statistics, Clinical Research , Regulatory , Observational Research , ... strategic solutions in support of internal stakeholder groups including the Outcomes Research and Clinical Safety organizations.Lead and actively contribute to… more
- Merck & Co. (North Wales, PA)
- …datasets, tables, listings, figures), the span of which range from individual clinical trials to world-wide regulatory application submissions and post marketing ... of statistical datasets that support multiple stakeholder groups which include clinical development, outcomes research and safety evaluation.The position is… more
- Novo Nordisk Inc. (Boulder, CO)
- …analytical and process development, the CMC team works alongside Quality, Regulatory , Technical Operations and RNAi Early Development professionals at our Boulder, ... well in a collaborative environment and be able to independently execute research across a wide range of oligonucleotide and organic chemistry projects.… more
- Novo Nordisk Inc. (Plainsboro, NJ)
- …Supervise designated personnel. Relationships Report to the Director/Associate Director/Lead Regulatory Scientist /Sr. Manager Regulatory Affairs. Develop ... About the Department The Clinical , Medical and Regulatory (CMR) department...NDA, Biologics, Devices) to government agencies in support of research and marketed products Create and maintain product/project database… more
- Merck & Co. (Rahway, NJ)
- Job DescriptionOur Clinical Research and Pharmacovigilance team push the boundaries of global healthcare through research and innovation. Through clinical ... and our company's guidelines and SOPs.Required Experience:5+ years of work experience in pre- clinical and/or clinical research to include minimum 2 years'… more
- Merck & Co. (Rahway, NJ)
- … expectations for small molecules and biologics in Oncology, authoring regulatory documents (investigational new drugs/INDs, clinical study reports (CSRs), ... clinical trial applications (CTDs)), and representing QP2-IO at regulatory meetings.- Minimum education required: Ph.D. with 1-3 years of pharmaceutical drug… more
- University of Washington (Seattle, WA)
- …and natural beauty. The Senior Scientist of Clinical and Regulatory Development ( Research Scientist /Engineer-Senior (ES 10)) will supervise technical ... action as needed. + Mentor staff to be highly competent on clinical and research regulatory requirements. + Coordinate continuing education and in-service… more
