- Daiichi Sankyo, Inc. (Basking Ridge, NJ)
- …an equal opportunity employer including veterans and people with disabilities. Summary The Associate Director , Clinical Data Standards, is responsible for ... - Leadership, Direction, and Strategy:Leads implementation of Therapeutic level clinical data collection requirements including cross-functional standards initiatives by… more
- Daiichi Sankyo, Inc. (Basking Ridge, NJ)
- …stud(ies).Ensures trial master file is complete and accurate for assigned stud(ies).If assigned, Associate Director , Clinical Operations may act as the Study ... regulations/EU Directive, and International Conference on Harmonization (ICH) guidelines. The Associate Director is accountable for operational planning and… more
- Daiichi Sankyo, Inc. (Basking Ridge, NJ)
- …an equal opportunity employer including veterans and people with disabilities. SummaryThe Associate Director , Global Oncology Clinical Development (GOCD) ... generation (checklist, process map, etc.), change management and detailed analyses. The Associate Director , GOCD Functional Excellence must have excellent verbal… more
- Merck & Co. (North Wales, PA)
- …of clinical data/medical protocol-deviations in collaboration with the Clinical Director .Builds talent and capabilities of direct/indirect team members ... years OR Master's + 6 years OR PhD/PharmD + 2 years Pharmaceutical and/or- clinical drug development experience. Degree in life sciences , preferred.NOTICE FOR… more
- Daiichi Sankyo, Inc. (Basking Ridge, NJ)
- …diversified, unmet medical needs of people globally by leveraging our world-class science and technology. With more than 120 years of scientific expertise and ... safety monitoring and risk management activities, provides insights on current clinical practice and guidelines, reviews and provides written assessments of relevant… more
- Daiichi Sankyo, Inc. (Basking Ridge, NJ)
- …in end-to-end clinical trial execution in one or more key functions (eg clinical research & development, clinical science , clinical quality ... medical needs of people globally by leveraging our world-class science and technology. With more than 100 years of...rare diseases and immune disorders. Summary The AD, Global Clinical Operations (GCO) Clinical Trial Operational Risk… more
- Daiichi Sankyo, Inc. (Basking Ridge, NJ)
- …diversified, unmet medical needs of people globally by leveraging our world-class science and technology. With more than 100 years of scientific expertise and ... centered around rare diseases and immune disorders.SummaryThis position serves as the Clinical Safety Scientist Lead for a large, late-stage program or multiple… more
- Daiichi Sankyo, Inc. (Basking Ridge, NJ)
- …an equal opportunity employer including veterans and people with disabilities.SummaryThe Associate Director will be responsible for developing and implementing ... of the following is required:PhD in Pharmacology or Pharmaceutical Sciences or PharmD with a clinical pharmacology...or Pharmaceutical Sciences or PharmD with a clinical pharmacology research fellowship and 4 years of relevant… more
- Daiichi Sankyo, Inc. (Basking Ridge, NJ)
- …other research areas centered around rare diseases and immune disorders.Summary The Associate Director , Global Clinical Operations (GCO) Procedural Ownership ... policies, and meet applicable ICH and GCP standards. The Associate Director will also be responsible for...or more key functions (eg clinical operations, clinical research, clinical science , and/or… more
- Daiichi Sankyo, Inc. (Basking Ridge, NJ)
- …diversified, unmet medical needs of people globally by leveraging our world-class science and technology. With more than 120 years of scientific expertise and ... teachings, and support related to risk management planning, risk management sciences , and risk management tools and resources.Responsibilities- Strategic Advice and… more
- Novo Nordisk Inc. (Plainsboro, NJ)
- …with Novo Nordisk policies and procedures. Relationships This position reports to a Senior Director within the Clinical Data Science & Evidence (CDSE) - ... About the Department The Clinical , Medical and Regulatory (CMR) department at Novo...you ready to make a difference? The Position The Associate Director , Research Partnerships (RP) is responsible… more
- Catalent (Harman, WV)
- Associate Director , Continuous ImprovementSummary:The Associate Director , Continuous Improvement will work collaboratively with the Sr Director of CI ... rapid adoption of best practices.Reporting to the CI Sr Director , this person is a dedicated resource responsible for...best practicesThe CandidateBachelor's degree with an emphasis in Life Science , Engineering or Business field7+ years of phase 3… more
- Daiichi Sankyo, Inc. (Basking Ridge, NJ)
- …diversified, unmet medical needs of people globally by leveraging our world-class science and technology. With more than 120 years of scientific expertise and ... and best practices as well as strong technical skills in working with ( clinical ) data. The position holder will require strong skills in continuous improvement,… more
- Merck & Co. (North Wales, PA)
- …of the role Preferred Experience and Skills: Ability to translate science / clinical data into clear marketing strategies, medical education and/or ... including experience including bringing materials through legal, regulatory, and clinical review Strong project management skills as demonstrated by prioritizing… more
- Daiichi Sankyo, Inc. (Basking Ridge, NJ)
- …required Experience Qualifications7 or More Years Minimum 7 years' experience in life sciences , pharma with Clinical Trials Operational Data, Clinical ... medical needs of people globally by leveraging our world-class science and technology. With more than 120 years of...milestones at Study, Country, and Site Level to gauge clinical trial performance. Build and Maintain Metrics Catalog, Dashboards… more
- Daiichi Sankyo, Inc. (Basking Ridge, NJ)
- …PartnerProvides scientific and technical expertise by collaborating closely with Translational Science Leads, Clinical Biomarker Leads, Biosample Operations, ... medical needs of people globally by leveraging our world-class science and technology. With more than 100 years of...Qualifications (from an accredited college or university)PhD in Life Sciences or in related discipline preferredMS degree in Life… more
- Daiichi Sankyo, Inc. (Basking Ridge, NJ)
- …research areas centered around rare diseases and immune disorders. Summary The Associate Director , Quantitative Systems Pharmacology (QSP) will work within the ... of therapeutic compounds. This includes working with scientists in Research, Translational Science , Clinical Development, in addition to colleagues in QCP. QSP… more
- Daiichi Sankyo, Inc. (Basking Ridge, NJ)
- …diversified, unmet medical needs of people globally by leveraging our world-class science and technology. With more than 120 years of scientific expertise and ... for diagnostics and devices.Provide strategic input on key development documents, clinical protocols, study reports, IBs, INDs, CTAs, IDEs, SRDs, PMAs and… more
- Merck & Co. (Rahway, NJ)
- …of the MACS EDFE Leader include the following:The EDFE Leader role at the Associate Director level will serve as a technical mentor and process team ... and GMP clinical manufacturing plant currently planned in Rahway, New Jersey. The Associate Director will serve as a team member of the MACS Center Basis… more
- Merck & Co. (Rahway, NJ)
- …of decision-making at our company, this position offers an opportunity for the Associate Director to drive pipeline impact across therapy areas.This Associate ... on a continuous basis in decision making and driving pipeline impact. The Associate Director will perform job duties independently with minimal supervision… more
