- Merck & Co. (Rahway, NJ)
- Job DescriptionPosition Description: Associate Director , Clinical Scientist This position drives scientific planning, strategy and execution of Phase 1-4 ... interpretation of clinical data/medical protocol-deviations in collaboration with the Clinical Director .Builds talent and capabilities of direct and indirect… more
- Merck & Co. (Rahway, NJ)
- …of clinical data/medical protocol deviations in collaboration with the Clinical Director .Builds talent and capabilities of direct/indirect team members ... capabilities through proactive coachingAdvanced communication, technical writing, and presentation skills. Education /ExperienceBachelor's Degree +9 years of pharmaceutical, clinical … more
- Daiichi Sankyo, Inc. (Bernards, NJ)
- …trial (small size, standard complexity in design and geographic scope). Prepares clinical section of regulatory document. Collaborates as team member with AROs/CROs. ... documents under guidance of higher level. Reviews and oversee completion of clinical trial protocols. Provides medical and/or scientific direction to Clinical … more
- Daiichi Sankyo, Inc. (Bernards, NJ)
- …centered around rare diseases and immune disorders.SummaryThis position serves as the Clinical Safety Scientist Lead for a large, late-stage program or multiple ... surveillance and risk management in partnership with Product Safety Lead(s), Clinical Safety Physician(s), and cross-functional team in support of benefit risk… more
- Daiichi Sankyo, Inc. (Bernards, NJ)
- …safety monitoring and risk management activities, provides insights on current clinical practice and guidelines, reviews and provides written assessments of relevant ... meet the qualifications below with or without a reasonable accommodation. Education Qualifications (from an accredited college or university)MD with board… more
- Merck & Co. (Rahway, NJ)
- Job DescriptionThe Senior Clinical Director (Sr. Principal Scientist) has primary responsibility for the strategic planning and directing clinical research ... investigational compounds in Immunology. With a focus on late-stage development, the Senior Clinical Director will manage the entire cycle of clinical … more
- Novo Nordisk Inc. (Plainsboro, NJ)
- …the head of Clinical , medical, Regulatory (CMR) Business Operations, the Associate Director (AD) is responsible for structuring facilitating and monitoring ... About the Department The Clinical , Medical and Regulatory (CMR) department at Novo...internal stakeholders. In the execution of specific projects, the Associate Director , will be accountable for managing… more
- Merck & Co. (Rahway, NJ)
- Job DescriptionThe Associate Director , Business Analyst, within Metrics, Analytics & Performance (MAP) will lead activities related to the development, delivery, ... monitor performance across our portfolio, studies & processes within Global Clinical Trial Operations (GCTO).Primary responsibilities include but are not limited… more
- Merck & Co. (North Wales, PA)
- …/Senior Director in the Office of Promotion and Advertising Review (OPAR)The Associate Director is responsible for the review and approval of all US ... support for anticipated promotional messages and claims (aligned with marketing strategy) in clinical trial design and product labeling as it relates to the use of… more
- Merck & Co. (North Wales, PA)
- …innovative medicines that help people with cancer across the globe.The Regional Associate Director of Medical Affairs - Gastrointestinal Cancer (RADMA) position ... with the Upper GI and Lower GI US Regional Director of Medical Affairs (RDMAs) and partner with regional...(advisory boards and Expert input forums) to address key clinical questions focused on improving patient careManages regional programs… more
- Merck & Co. (North Wales, PA)
- Job DescriptionJob Description:The Associate Director , Marketing, HPV Scientific Strategy plays a critical role in supporting the HPV vaccine franchise.- The HPV ... opportunities.Collaborating with Global Medical and Scientific Affairs (GMSA), US, Senior Director of Medical Affairs (SDMA), Center for Observational and Real-world… more
- Daiichi Sankyo, Inc. (Bernards, NJ)
- …research areas centered around rare diseases and immune disorders. Summary The Associate Director Global Oncology Strategic Planning provides strategic insights ... are tracked and ensure implications are assessed and communicated on timely manner- Clinical Development Life Cycle Management Decision Support: Be the key point of… more
- Merck & Co. (North Wales, PA)
- Job DescriptionUnder the guidance of a senior leader, an Associate Principal Scientist has primary responsibility for planning/managing real world and outcomes ... requirements to inform value evidence and outcomes research strategies.Requirements for Education , Experience and SkillsAdvanced or professional degree in a relevant… more
- Daiichi Sankyo, Inc. (Bernards, NJ)
- …delivery of training, and ensuring training materials enable continuous education , and driving process and system adoption within CSPVCollaborate cross-functionally ... meet the qualifications below with or without a reasonable accommodation. Education Qualifications (from an accredited college or university)- Bachelor's Degree… more
- Daiichi Sankyo, Inc. (Bernards, NJ)
- …and technical expertise by collaborating closely with Translational Science Leads, Clinical Biomarker Leads, Biosample Operations, Clinical Leads and Regulatory ... landscape Qualifications: (What are the minimum requirements for the position?) Education :PhD in Life Sciences or in related discipline preferred.MS degree in… more
- Daiichi Sankyo, Inc. (Bernards, NJ)
- …technical teams in preparation of submission documents to include clinical trial applications/amendments (eg, IND, IMPD, IB) and marketing applications/supplements ... laboratory members, the Contract Manufacturing Organization (CMO), Labeling members and Clinical members. This position works with non-standard problems of some… more
- Merck & Co. (Boston, MA)
- …that accelerate the decision-making process from hit identification to clinical candidate delivery across different therapeutic areas and modalities at ... impact on pipeline and capability deliverables. Position Qualifications : Education Minimum Requirement: Ph.D., Master's, or Bachelor's degree in cheminformatics,… more
- Daiichi Sankyo, Inc. (Bernards, NJ)
- …to meet the qualifications below with or without a reasonable accommodation. Education (from an accredited college or university)- Bachelor's Degree required- ... preferred Experience- 7 or More Years Outsourcing, health sciences or related field ( clinical trials) required- 7 or More Years Deep experience in pharma procurement… more
- Daiichi Sankyo, Inc. (Bernards, NJ)
- …Statistical Analysis Plan (SAP), Statistical Analysis, Results Interpretation, and clinical study report (CSR): Leads statistical activities for complex studies ... to meet the qualifications below with or without a reasonable accommodation. Education Qualifications (from an accredited college or university)PhD in statistics or… more
- Daiichi Sankyo, Inc. (Bernards, NJ)
- …those involving 3rd party development. This position partners with GRLs and Clinical Safety Pharmacovigilance (CSPV) leads in the maintenance of Company Core Data ... meet the qualifications below with or without a reasonable accommodation. Education Qualifications (from an accredited college or university)Bachelor's Degree… more
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