- Merck & Co. (Rahway, NJ)
- …to: Collaborate closely with biomarker scientists and project teams to plan clinical trial biomarker set-up using logistical strategies to ensure efficient ... Preferred Experience and Skills: Drug discovery experience, including familiarity with clinical trial execution in Oncology studies. Biomarker assay experience… more
- Daiichi Sankyo, Inc. (Bernards, NJ)
- …submission documents under guidance of higher level. Reviews and oversee completion of clinical trial protocols. Provides medical and/or scientific direction to ... providing novel therapies in oncology, as well as other research areas centered around rare diseases and immune disorders....Planning and Execution: Provides input on major milestones of trial , clinical trial plan and… more
- Merck & Co. (Rahway, NJ)
- …development and qualification of release, characterization, and stability assays for testing of clinical trial material and in support of product and process ... Job DescriptionPosition Description: Associate Principal Scientist, Biologics Analytical Research and Development (Onsite) The Biologics Analytical Research … more
- Merck & Co. (Rahway, NJ)
- …the clinical /scientific execution of clinical protocol(s).Serves as the lead clinical scientist on the clinical trial team.Collaborates with the ... manage scientific activities on clinical protocols.Apply strong knowledge of clinical research regulatory requirements (eg, GCP and ICH)Manage multiple… more
- Merck & Co. (North Wales, PA)
- …and other company Research Laboratories Scientists in designing and analyzing clinical trials , and in coordinating the statistical activities for clinical ... problems arising in the design, conduct, and analysis of clinical trials , proposes solutions and carries them... activities for innovative statistical methods and applications in clinical trial development.Mentors and guides junior staff… more
- Novo Nordisk Inc. (Plainsboro, NJ)
- …with Supplier Management, Research Administration, Grant Operations, Grant Management, clinical trial management, or a similar research operations ... schedules) Advanced knowledge of regulatory and compliance requirements for clinical research , ICH GCP Principles and the...to trial design, planning & conduct of clinical trials Advanced capability in MS Excel,… more
- Merck & Co. (North Wales, PA)
- …knowledge, statistical-analysis and high-quality data to support decision making in clinical trials .-The Associate Principal Scientist, Statistical ... Job DescriptionI n BARDS (Biostatistics and Research Decision Sciences), a distinguished department within our...or more years of SAS programming experience in a clinical trial environmentMS in Computer Science, Statistics,… more
- Merck & Co. (North Wales, PA)
- …of 9 years Statistical Analysis System (SAS) programming experience in a clinical trial environment.MS (preferred) in Computer Science, Statistics, Applied ... of 7 years Statistical Analysis System (SAS) programming experience in a clinical trial environment. Required-Experience and Skills: Proven track record for… more
- Merck & Co. (Rahway, NJ)
- …or related field plus 9 years SAS/R programming experience in a clinical trial environmentMS in Computer Science, Statistics, Applied Mathematics, Life ... Job DescriptionPosition Description: Associate Principal Statistical Programmer - Oncology (Hybrid) In...7 or more years SAS/R programming experience in a clinical trial environmentRequired Experience and Skills: Excellent… more
- Merck & Co. (Rahway, NJ)
- …Required Experience and Skills Strong writing skills and competence in biomedical research General Medicine clinical trial publications experience ... presentations that report results from our company's General Medicine clinical trial program, as well as select...as select early-stage development projects and other of our Research & Development Division science. The Associate … 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 ... or related field plus 9 years SAS programming experience in a clinical trial environment.MS in Computer Science, Statistics, Applied Mathematics, Life… more
- Merck & Co. (North Wales, PA)
- …Engineering or related field plus 9 years SAS programming experience in a clinical trial environmentMS in Computer Science, Statistics, Applied Mathematics, Life ... field plus 7 or more years SAS programming experience in a clinical trial environmentDepartment Required Skills and Experience: Excellent interpersonal skills… more
- Merck & Co. (Rahway, NJ)
- …Mass Spectrometry based assays that are deployed in support of clinical trials . The candidate for this Associate Principal Scientist position should have ... assays across all therapeutic areas and all phases of clinical development at our Company Research laboratories....clinical development to execute on biomarker strategies in clinical trials .Writing memos, final reports and publications… more
- Merck & Co. (Rahway, NJ)
- …optimal trial design and monitoring of studies, producing high-quality clinical documents and presentations. The position requires a solid understanding of the ... Job DescriptionThe Associate Vice President (AVP)/ Metabolism Section Head in...research and business development priorities and prioritization of clinical assetsMay serve as the senior liaison for relevant… more
- Novo Nordisk Inc. (Plainsboro, NJ)
- …actual product Responsible for all areas related to patient safety in clinical trials Act as member of the trial safety group for dose escalation decisions ... and Seattle reflect the full R&D continuum, from early research through late-stage clinical development. Here, we...) Provide safety input to Product Development Plan (PDP), Trial Outline, Protocol, Clinical Trial … more
- Merck & Co. (Rahway, NJ)
- …processes for diverse biotherapeutics, and efficiently manufacture material to supply clinical trials . We are also responsible for commercial process ... Job DescriptionThe Biologics Process Research & Development organization within our company's ...our Downstream Process Development and Engineering group as an Associate Principal Scientist.- In this role, you will work… more
- Eisai, Inc (Baltimore, MD)
- …and other international regulatory/ethical guidelines relevant to the pharmaceutical industry & clinical trial conduct, and to ensure compliance with these ... in neurology and oncology, with a strong emphasis on research and development. Our history includes the development of...your profile, we want to hear from you. The Associate Director/Director, MSLs is responsible for the leadership, direction… more
- Merck & Co. (North Wales, PA)
- …support for anticipated promotional messages and claims (aligned with marketing strategy) in clinical trial design and product labeling as it relates to the ... the Director/Senior Director in the Office of Promotion and Advertising Review (OPAR)The Associate Director is responsible for the review and approval of all US… more
- Daiichi Sankyo, Inc. (Bernards, NJ)
- …and leads technical teams in preparation of submission documents to include clinical trial applications/amendments (eg, IND, IMPD, IB) and marketing ... focused on providing novel therapies in oncology, as well as other research areas centered around rare diseases and immune disorders.Job Summary: This position… more
- Daiichi Sankyo, Inc. (Bernards, NJ)
- …preferred Experience- 7 or More Years Outsourcing, health sciences or related field ( clinical trials ) required- 7 or More Years Deep experience in pharma ... & category management required- CRO experience preferred- Strong knowledge of clinical trials preferred- Demonstrated ability to leverage digital data… more
