- Merck & Co. (Rahway, NJ)
- …interpretation of clinical data/medical protocol-deviations in collaboration with the Clinical Director .Builds talent and capabilities of direct and indirect ... Job DescriptionPosition Description: Associate Director , Clinical Scientist This position drives scientific planning, strategy and execution of Phase 1-4 … more
- Insmed Incorporated (San Diego, CA)
- …for Millennials™, and Best Medium Workplaces™ lists.OverviewThe Executive Medical Director of Ophthalmology, Clinical Development holds the responsibility ... to lead clinical programs across different diseases and supervise the clinical development team. This individual will be the primary point person for medical… more
- CHRISTUS Health (Tyler, TX)
- …expenses Documents capital appropriations and project authorizations Standard II. Human Resources Management Evaluates and specifies the critical resources ... required to accomplish the team's objectives Initiates requests for required resources based on staff competency with patient acuity Allocates team resources … more
- Novo Nordisk Inc. (Plainsboro, NJ)
- …Leaders/National Expert Panels for select clinical trials, in collaboration with Clinical Director and Clinical Operations lead Support investigator ... Clinical Trial Strategy Team in collaboration with Clinical Operations point, Clinical Director ,...Medical Affairs team on relevant disease state topics and clinical trial data. Review and approve resources … more
- Merck & Co. (Boston, MA)
- …questions and directs SL inquiries on issues outside of Regional Medical Scientific Director scope (eg, grants) to appropriate company resources consistent with ... in the assigned territory (Boston area).Role SummaryThe Oncology Regional Medical Scientific Director - Head & Neck Cancers/Melanoma is a credentialed (ie, PhD,… more
- Novo Nordisk Inc. (Plainsboro, NJ)
- About the Department The Clinical , Medical and Regulatory (CMR) department at Novo Nordisk is one of the most diverse and collaborative groups within the ... Assigned staff members of Medical Information (MI) report to the Associate Director . The Associate Director communicates medical information to a large… more
- Eisai, Inc (Baltimore, MD)
- …If this is your profile, we want to hear from you. The Associate Director / Director , MSLs is responsible for the leadership, direction and management of MSLs ... with strategic and tactical planning, working collaboratively with Medical Affairs and Clinical Development teams for support of clinical studies across the… more
- Tris Pharma (Monmouth Junction, NJ)
- …and product launch. We have a position available for a Senior Director / Director , National Sales (NSD) to lead approximately 100-person pharmaceutical sales ... effectively deliver information on our products to Healthcare Professionals.The Senior Director / Director , National Sales (Sr NSD) provides leadership, direction… more
- Novo Nordisk Inc. (Plainsboro, NJ)
- …and Seattle reflect the full R&D continuum, from early research through late-stage clinical development. Here, we are building for the future, creating a distinct ... R&D hub merges biotech speed and agility with large pharmaceutical company quality, resources , and stability, uniting the best of both worlds to develop new… more
- Daiichi Sankyo, Inc. (Bernards, NJ)
- …group and high-complexity disease work to support critical strategic choices for the clinical program. The DAST Director will collaborate with the DAST Lead ... and core DAST membership to build out disease-focused resources and capabilities. The individual will be a key contributor to a unified Disease Area Strategy across… more
- Legend Biotech USA, Inc. (Raritan, NJ)
- …in the treatment of multiple myeloma.Legend Biotech is seeking an Associate Director of Quality Project Management and Strategyas part of the Quality team ... based in Raritan, NJ. Role OverviewThe Associate Director of Quality Project Management and Strategy role is...within a cell therapy manufacturing facility to support both clinical and commercial requirements in a sterile GMP environment.… more
- Novo Nordisk Inc. (Plainsboro, NJ)
- …MA and Plainsboro, NJ. We support programs from early research through late-stage clinical development. We are building for the future, creating a distinct R&D ... Development Hub merges biotech speed and agility with large pharmaceutical company quality, resources , and stability, uniting the best of both worlds to develop new… more
- Daiichi Sankyo, Inc. (Bernards, NJ)
- …centered around rare diseases and immune disorders. Summary The Associate Director Global Oncology Strategic Planning provides strategic insights and direction on ... input into the annual R&D Pipeline prioritization process to ensure DS's R&D resources are appropriately invested. The position will also serve as the Lead in… more
- Merck & Co. (San Diego, CA)
- …models using a combination of our Company's proprietary data assets and public data resources , to generate novel CDx models that can be deployed in clinical ... trials. You will also support preparation of regulatory documents in support of clinical trials.- In addition, you will be the site lead for the DAGS function at San… more
- Daiichi Sankyo, Inc. (Bernards, NJ)
- …and / or develops operational resource strategy to determine the extent of resources needed to deliver on GLP/GCLP commitments that are pivotal to early phase ... quality system that supports quality and compliance of Good Clinical Laboratory Practices and Good Laboratory Practices. Proactively identifies compliance… more
- Daiichi Sankyo, Inc. (Bernards, NJ)
- …labeling in collaboration with the Global Regulatory Leads (GRLs) and Clinical Safety & Pharmacovigilance (CSPV) for assigned products. This position drives/leads ... those involving 3rd party development. This position partners with GRLs and Clinical Safety Pharmacovigilance (CSPV) leads in the maintenance of Company Core Data… more
- Novo Nordisk Inc. (Plainsboro, NJ)
- …inclusion in our clinical portfolio. Relationship This role reports into the Director of Clinical Research Equity supporting the strategy across NACD. This ... to the needs of patients, sites, and caregivers With Director , serve as NACD SME on clinical ...with policymakers and community leaders to effect change Develop resources and/or support training for NN staff and/or healthcare… more
- Daiichi Sankyo, Inc. (Bernards, NJ)
- …US, EU, Japan, and other global sites. These business functions include: Clinical Operations, Clinical Development, Biostatistics and Data Management, Regulatory ... Affairs, Quantitative Clinical Pharmacology, Clinical Safety and Pharmacovigilance, Regulatory/Risk...develop business cases to secure the necessary funding and resources for their successful implementation. Accountable for managing Technology… 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 ... teams on global labeling issues. Based on timelines or resources , may assist another Global Labeling Lead by managing...teams on RA labeling issues. Based on timelines or resources , may assist another Global Labeling Lead by managing… more
- Novo Nordisk Inc. (Minneapolis, MN)
- …and community thought-leaders in an assigned territory. The Rare Renal Clinical Account Manager will be principally responsible for driving disease awareness, ... leader in the rare renal marketplace. The Rare Renal Clinical Account Manager (RRCAM) will be responsible for achieving...Novo Nordisk. The role reports to the Regional Business Director for Rare Renal and interacts internally with other… more
