- Aequor (Thousand Oaks, CA)
- TTitle: Project Manager - Science Education & Community Must be local Thousand Oaks, CA campus and willing to come onsite a few days per month. Part time role, 20 ... hours/week. Duration: 1 year We are seeking a part-time Project Manager with a strong background in education and the life sciences, not pharmaceuticals. This… more
- Daiichi Sankyo, Inc. (Bernards, NJ)
- …is primarily focused on providing novel therapies in oncology, as well as other research areas centered around rare diseases and immune disorders. Job Summary: The ... Manager , Internal Process Audits is responsible for end-to-end GxP...stakeholders in identifying and defining quality improvement initiatives for development activities / programs post internal system audit.Support reporting… more
- Merck & Co. (San Francisco, CA)
- …or more of the areas of Drug Substance development , Drug Product development , Clinical Supply management or Analytical Research is critical for understanding ... Description: Associate Director, DSCS Digital Implementation Project ManagerWithin the Development Sciences and Clinical Supply (DSCS) organization, the Digital… more
- Merck & Co. (North Wales, PA)
- …global, cross-functional team. You will build and coach your team in the development of project management, communication, and collaboration skills in support of our ... Team lead. Leads and directs teams in key study planning, development , and execution elements (eg operational reviews, issue escalation/mitigations, presentations at… more
- Merck & Co. (North Wales, PA)
- …the clinical trial team leadMay lead team in key study planning, development , and execution elements (eg, data management deliverables, trial level plans/timelines, ... study specific partners and/or vendors.Core Skills: Solid knowledge of clinical research regulatory requirements (eg, GCP and ICH)Ability to manage multiple… more
- Taiho Oncology (FL)
- …on Taiho products and relevant disease states, and facilitation of clinical research . The Sr. Manager , Medical Field integrates clinical/scientific expertise and ... PR, AL Formally known as Medical Science Liaison Position Summary: The Sr. Manager , Medical Field is a field-facing representative of the Medical Affairs Department… more
- Formation Bio (New York, NY)
- …help execute on our tech strategy through 0-to-1 product conceptualization, rigorous research and experimentation, and iterative development of new products. You ... and AI driven pharma company differentiated by radically more efficient drug development . Advancements in AI and drug discovery are creating more candidate drugs… more
- Novo Nordisk Inc. (Plainsboro, NJ)
- …health outcomes. Are you ready to realize your potential? The Position The Manager - Market Access Insights assesses product and customer performance for all ... groups, contributing to manage markets strategy decisions, and is responsible for development and maintenance of a repository of strategy lessons and best-… more
- Daiichi Sankyo, Inc. (Bernards, NJ)
- …with key stakeholders within CSPV and external functions including Clinical Development , Research Development , Regulatory Affairs.Facilitate operational ... primarily focused on providing novel therapies in oncology, as well as other research areas centered around rare diseases and immune disorders. Job Summary: Manage… more
- Novo Nordisk Inc. (Boston, MA)
- …and new areas. The STARS team collaborates and partners with groups across NAO, Research & Early Development , Development , innovation hubs across NN, other ... portfolio. The mandate of STARS is to facilitate the development and to coordinate the execution of the long-term...this job family are as follows: Rare Endocrine Therapy Manager $ 96,670 to $ 178,840 Sr Rare Endocrine… more
- Daiichi Sankyo, Inc. (Bernards, NJ)
- …primarily focused on providing novel therapies in oncology, as well as other research areas centered around rare diseases and immune disorders. SummaryThe Manager ... eQMS in a timely manner.Support CAPA completion for all outsourced audits with Development and Medical QA, PV QA, QMS and stakeholders.Collaborate with QMS Team and… more
- ACROBiosystems Inc. (San Diego, CA)
- …manufacturing recombinant proteins and critical reagents/assays to support drug development and clinical applications from target discovery and validation, candidate ... drug screening and optimization, CMC development , preclinical and clinical studies, commercial production, and companion diagnostics. We are committed to excellence… more
- Daiichi Sankyo, Inc. (Bernards, NJ)
- …focused on providing novel therapies in oncology, as well as other research areas centered around rare diseases and immune disordersJob Summary: The Regulatory ... Process Manager will be a key member of the Global...and cross-functional teams (eg, Quality, CSPV, Clinical Operations, Clinical Development , RA CMC) to keep processes, procedural documents and… more
- Merck & Co. (North Wales, PA)
- … Decision Sciences (BARDS), a distinguished department within our renowned Research and Development division, quantitative scientists, in partnership with ... art scientific methodologies and tools to enable the discovery, development , regulatory approval, manufacturing, and marketing of medical drugs...and maintaining high performing teams both as a direct manager and a second line manager (ie,… more
- Merck & Co. (North Wales, PA)
- …with the Clinical Director.Other responsibilities include:Collaborating cross-functionally in the development of Protocol and related study materials (eg, ICF ... documents / amendments); Partners with the Study Manager on study deliverables.Ensuring CRF design supports data collection in alignment with the protocol in… more
- Merck & Co. (Rahway, NJ)
- …with the Clinical Director. Other responsibilities include: Collaborating cross-functionally in the development of Protocol and related study materials (e . g . , ... ICF documents/ amendments); Partners with the Study Manager on study deliverables. Ensuring CRF design supports data...other clinical scientists. Core Skills Solid knowledge of clinical research regulatory requirements (e . g . , GCP… more
- Merck & Co. (Rahway, NJ)
- Job Description Job Description The Rahway based Senior Specialist, Global Development Quality Operations - API, is responsible for independent review and approval ... assurance activities related to API manufacturing in a complex, clinical supply development .- Review and/or approve GMP documents. Ensure all API are manufactured in… more
- Merck & Co. (KY)
- …to understand practice structure, business model, key influencers (Owner/Practice Manager /Key Tech/Associate Vet/Front office staff), customer needs and identifies ... portfolio.Shares with other team members within the region to foster growth and development within the team.Analyze sales results on a monthly basis and manage… more
- Merck & Co. (Rahway, NJ)
- …primarily for sterile operations under the remit of Our Company's Research Labs Pharmaceutical Sciences (Pharm Sci), Pharmaceutical Operations Engineering group ... including critical program needs related to new products undergoing process development , new products undergoing scale-up, launch and transfer to the supply… more
- Merck & Co. (Rahway, NJ)
- …and forecasting.Communicate IT strategy and portfolio to key stakeholders in our Research & Development Division and IT.- Encourage a digital mindset ... We partner internationally to deliver the services and solutions that help development scientists to be more productive and enable innovation.The BTP ensures… more
