- Merck & Co. (San Francisco, CA)
- …the Development Sciences and Clinical Supply (DSCS) organization, the Digital Project Manager will streamline the execution of our Company's DSCS Digital ... capacity and robustness across organizational deliverables.- In this role, the DSCS Digital Project Manager will provide tactical direction and partner with the… more
- Merck & Co. (North Wales, PA)
- …writing, and presentation skillsEducation/ExperienceBachelor's Degree +5 years of pharmaceutical, clinical drug development, project management, and/or medical ... field experience OR Master's Degree +3 year of pharmaceutical, clinical drug development, project management, and/or medical field experience OR PhD/PharmD… 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
- 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
- Eisai, Inc (Nutley, NJ)
- …is your profile, we want to hear from you. The Associate Director, Clinical Programming must have expertise in addressing technical challenges in the programming ... Associate Director must be a highly specialized individual contributor or functional manager with advanced knowledge and expertise to analyze assess and initiate… 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
- 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 ... to internal audits and inspections Demonstrate leadership skills via acting as project lead on cross-functional projects in the development and/or implementation of… 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 ... to internal audits and inspections Demonstrate leadership skills via acting as project lead on cross-functional projects in the development and/or implementation of… 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 ... various areas of the business Demonstrate leadership skills via acting as project lead on cross-functional projects in the development and/or implementation of… more
- BioAgilytix (San Diego, CA)
- …analysis.Write and review reports and prepare SOPs.Fulfill the role of Bioanalytical Project Manager (BPM)/Principal Investigator (PI) for all assigned clients ... you enable life-changing, life-saving therapeutics to the patients who need them.The Manager II will lead scientific and operational activities in support of… more
- Genmab (NJ)
- …in-house checks of data consistenciesSupports specification and pooling of data across clinical trials within the same project .Supports in-house production of ... we would love to have you join us!The Programming Manager supports the development of new therapies by ensuring...will support the Data Management, Statistics, Drug Safety, Medical, Clinical Pharmacology and Biomarker functions with the above by… more
- ACROBiosystems Inc. (San Diego, CA)
- …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 in providing… more
- Merck & Co. (Rahway, NJ)
- … Project management.-Track-record of independent problem-solvingSAP Training and skills - Project Manager (PM) role, SAP Plant Maintenance (Gatekeeping and ... Engineering Lead of the FLEx GMP facility within Pharmaceutical Operations and Clinical Supply (PSCS)The FLEx sterile facility supports the formulation and filling… more
- Merck & Co. (Rahway, NJ)
- …review and approval of documentation to support Good Manufacturing Practice (GMP) clinical supply API manufacture, testing, release, and maintenance in support of ... our company's clinical supply programs. This person will also independently review...and CAPAs. Support quality risk management activities as facilitator, project lead and/or quality subject matter expert. Proactively identify,… more
- Formation Bio (New York, NY)
- …than the industry can progress because of the high cost and time of clinical trials. Recognizing that this development bottleneck may ultimately limit the number of ... processes, and capabilities to accelerate all aspects of drug development and clinical trials. Formation Bio partners, acquires, or in-licenses drugs from pharma… more
- BioAgilytix (Durham, NC)
- …(LC/MS) team is seeking a Scientist III to serve as Bioanalytical Project Manager (BPM)/Principal Investigator (PI), overseeing all aspects of bioanalytical ... that shape the future of healthcare.Essential Responsibilities:Serve as Bioanalytical Project Manager (BPM)/Principal Investigator (PI), overseeing all aspects… more
- Merck & Co. (North Wales, PA)
- …President in BARDS and will work collaboratively with other leaders in Clinical Development and Global Regulatory Affairs.--The AVP provides leadership and direction ... skills, expertise in leading large teams in the development of novel clinical trial designs and analysis methods in oncology, experience in directing multiple… more
- Legend Biotech USA, Inc. (Raritan, NJ)
- …for overseeing the production of a personalized cell therapy to support both clinical and commercial requirements in either a Grade C or sterile cGMP environment.Key ... schedules.Will have 3-6 direct reports ranging from Associate Director, Senior Manager , and Manager .Oversee the hiring, development, and performance management… more
- Merck & Co. (Rahway, NJ)
- …strategic digital roadmaps, and lead delivery of capital project digital programs.Responsibilities include:Planning and allocating resources for cross-product ... delivery and coordinating with investment Manager to ensure appropriate coordination and forecasting.Communicate IT strategy and portfolio to key stakeholders in our… more
- Daiichi Sankyo, Inc. (Bernards, NJ)
- …manufacturing organizations CMO. This position serves as the Regulatory Affairs (RA) CMC project representative to the CMC sub team and the RA team and serves ... as ad hoc member to the Global Project Team for late stage projects. This position manages...technical teams in preparation of submission documents to include clinical trial applications/amendments (eg, IND, IMPD, IB) and marketing… more
