- Merck & Co. (Rahway, NJ)
- …Driving License:NoHazardous Material(s):n/aRequired Skills:Adaptability, Adaptability, Business , Business Risks, Change Management, Clinical Development ... development teams and the operational/executional arms within the business .-- - - The Program Clinical Supplies Project Manager (Program CSPM) serves as… more
- Merck & Co. (Rahway, NJ)
- …- DayValid Driving License:NoHazardous Material(s):n/aRequired Skills:Adaptability, Adaptability, Business Risks, Change Management, Clinical ... sites globally. The GCS Planning (Planning) organization is the key interface between clinical development teams and the operational/executional arms within the … more
- Merck & Co. (Rahway, NJ)
- … clinical development teams and the operational/executional arms within the business .-- - - Working independently, the Protocol Clinical Supplies Project ... GCS and serve s as the GCS spokesperson at clinical development related meetings (i .e., ...problems, make informed risk decisions considering both technical & business risks, & influence portfolio decisions with facts and… more
- Merck & Co. (North Wales, PA)
- … data/medical protocol deviations in collaborations with the Clinical Director.Other responsibilities include:Collaborating cross-functionally in the development ... writing, and presentation skillsEducation/ExperienceBachelor's Degree +5 years of pharmaceutical, clinical drug development , project management, and/or medical… more
- Merck & Co. (Rahway, NJ)
- …presentation skills - Education/Experience Bachelor's Degree +5 years of pharmaceutical , clinical drug development , project management , and/or medical field ... . , ICF documents/ amendments); Partners with the Study Manager on study deliverables. Ensuring CRF design supports data...OR Master ' s Degree +3 year of pharmaceutical, clinical drug development , project management, and/or medical… 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 ... and collecting data to support efficacy and new product development , CMR is involved. The one thing that keeps...The Position Developing quality and strategic objectives and strong business understanding of the value chain and customer focus.… 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 ... and collecting data to support efficacy and new product development , CMR is involved. The one thing that keeps...The Position Developing quality and strategic objectives and strong business understanding of the value chain and customer focus.… more
- Merck & Co. (North Wales, PA)
- …PowerPoint, Word, Outlook, etc.)Education/ExperienceBachelor's Degree +9 years of pharmaceutical, clinical drug development , project management, and/or medical ... field experienceOR Master's Degree +6 year of pharmaceutical, clinical drug development , project management, and/or medical field experienceOR PhD/PharmD Degree… more
- Merck & Co. (San Francisco, CA)
- …DSCS Digital Implementation Project ManagerWithin the Development Sciences and Clinical Supply (DSCS) organization, the Digital Project Manager will ... Travel Requirements: Flexible Work Arrangements:HybridShift:Valid Driving License:Hazardous Material(s):Required Skills:Budget Development , Business , Clinical Supply Chain… 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 ... and collecting data to support efficacy and new product development , CMR is involved. The one thing that keeps...for developing Quality and USO strategic objectives and strong business understanding of the value chain and customer focus,… more
- Merck & Co. (North Wales, PA)
- …Word, Outlook, etc.)Education/Experience: Bachelor's Degree +5 years of pharmaceutical, clinical drug development , project management, and/or medical field ... experience/ Master's degree +3 year of pharmaceutical, clinical drug development , project management, and/or medical field experience or PhD/PharmD DegreeDegree… more
- Lundbeck (Fort Wayne, IN)
- …the way in creating positive customer experiences! As a BioPharmaceuticals Account Manager , you lead the promotion of our infusion product, driving demand creation ... by providing comprehensive clinical knowledge, executing sales and marketing strategies in the...demonstrate strong capability in the following areas: ESSENTIAL FUNCTIONS: Business Planning & Account Leadership - Ability to use… more
- Lundbeck (Joliet, IL)
- …transform lives. Join us on our journey of growth! As a Psychiatry Account Manager , you lead the promotion of our psychiatry portfolio, executing sales and marketing ... strategies with comprehensive clinical knowledge to drive sales performance. Our Account Managers...demonstrate strong capability in the following areas: ESSENTIAL FUNCTIONS: Business Planning & Account Leadership - Ability to use… more
- Lundbeck (Waco, TX)
- …to stakeholders in the primary care and neurology settings. As an Account Manager , you lead the promotion of our psychiatry portfolio, executing sales and marketing ... strategies with comprehensive clinical knowledge to drive sales performance. Our Account Managers...demonstrate strong capability in the following areas: ESSENTIAL FUNCTIONS: Business Planning & Account Leadership - Ability to use… more
- Genmab (NJ)
- …Role:The Senior Statistical Manager acts as a biostatistician supporting the clinical development of compounds as compound lead, primarily up until proof ... synopsis, protocols, statistical analysis plans, results meetings presentations and clinical trial reportsCoordinate data transfers from/to business partners… more
- Daiichi Sankyo, Inc. (Bernards, NJ)
- …have at least 7 or more years of professional experience in Quality and clinical development in the Pharmaceutical industry, with involvement in regulated ... research areas centered around rare diseases and immune disorders. SummaryThe Manager Audits & Compliance, GCP/Document Audits supports end-to-end audit activities… more
- Daiichi Sankyo, Inc. (Bernards, NJ)
- …relationships with key stakeholders within CSPV and external functions including Clinical Development , Research Development , Regulatory Affairs.Facilitate ... and monitor performance of vendors against service level and KPIs.Manage the development of governance, business continuity, quality, and vendor monitoring… more
- Genmab (NJ)
- …components of regulatory submission (NDA, BLA, MAA) highly preferred.Solid understanding of clinical development and regulatory frameworks, including GCP and ICH ... employees.Our people are compassionate, candid, and purposeful, and our business is innovative and rooted in science. We believe...our Global Medical Writing team, you will drive the development of high-quality clinical documents to support… more
- Genmab (NJ)
- …feel like a fit? Then we would love to have you join us!The Programming Manager supports the development of new therapies by ensuring integrity, consistency and ... families and employees.Our people are compassionate, candid, and purposeful, and our business is innovative and rooted in science. We believe that being proudly… more
- Daiichi Sankyo, Inc. (Bernards, NJ)
- …will work with Global Regulatory Affairs and cross-functional teams (eg, Quality, CSPV, Clinical Operations, Clinical Development , RA CMC) to keep processes, ... rare diseases and immune disordersJob Summary: The Regulatory Process Manager will be a key member of the Global...and review data/metrics with the GRA Analytics TeamCoordinate the development and roll-out of training for changes to processes… more
