- Jazz Pharmaceuticals (Philadelphia, PA)
- …[clinical and medical affairs], data science, regulatory, clinical development, medical writing , and other vital functions and represent Statistical ... information, please visit and follow @JazzPharma on Twitter. The Director will be responsible for managing the product leaders...but not limited to: Deliver the cross-functional process improvement projects as the single point of contact and or… more
- Eisai, Inc (NJ)
- …preparing PCS, protocols, and protocol amendments often acting as the compound leadLead project management for medical writing deliverable by defining ... this is your profile, we want to hear from you. Job Summary The Senior Manager, Medical Writing will be the designated Lead Medical Writer for approximately… more
- Daiichi Sankyo, Inc. (Basking Ridge, NJ)
- …and amendmentsLead document review and coordination for the protocol and amendments. Additional medical writing tasks may involve ICF, CRF guidelines, IB and ... pharmaceutical therapies to improve standards of care and address diversified, unmet medical needs of people globally by leveraging our world-class science and… more
- Merck & Co. (North Wales, PA)
- …IS A HYBRID ROLE. AN ONSITE PRESENCE IS REQUIRED The Global Medical Information (GMI) Scientists for Oncology, with their advanced scientific background (PharmD, ... are resources within their therapeutic area for the global core functions of Medical Information (eg, customizing medical information letters to respond to US… more
- Daiichi Sankyo, Inc. (Basking Ridge, NJ)
- …for managing the multiple Clinical Science Asset Leaders (CSALs) at the Senior Director level for each respective programThis Clinical Science (CS) Group Lead will ... are managing a team of clinical scientists for the writing of protocols / amendments and associated documents (...clinical data and Clinical Study Reports (CSRs)/outputs throughout the project life cycle is optimized across multiple programsThe CS… more
- Daiichi Sankyo, Inc. (Basking Ridge, NJ)
- …pharmaceutical therapies to improve standards of care and address diversified, unmet medical needs of people globally by leveraging our world-class science and ... strategic leadership for all statistical programming activity related to study, project and submissionManage CRO to ensure high quality compound and multi-compound… more
- Eisai, Inc (Nutley, NJ)
- …and communication skills (both written and verbal).Demonstrated ability to lead global project teams to deliver projects across therapeutic areas, preferably in ... At Eisai, satisfying unmet medical needs and increasing the benefits healthcare provides...support of staff. Some travel may be required for project management and/or business development.The incumbent is expected to… more
- Eisai, Inc (Nutley, NJ)
- …of neurodegenerative disorders, eg, Alzheimer's disease and dementia, and other projects .Collaborate with cross-functional partners to meet project deliverables ... At Eisai, satisfying unmet medical needs and increasing the benefits healthcare provides...related to Alzheimer's disease (AD) dementia and various other projects . In this capacity, you will engage in collaborative… more
- Daiichi Sankyo, Inc. (Basking Ridge, NJ)
- …implementation of sourcing strategies for a specific set of R&D categories (CRO, Medical Writing , BDM, etc..). Builds strategic plans for specific categories ... pharmaceutical therapies to improve standards of care and address diversified, unmet medical needs of people globally by leveraging our world-class science and… more
- Daiichi Sankyo, Inc. (Basking Ridge, NJ)
- …pharmaceutical therapies to improve standards of care and address diversified, unmet medical needs of people globally by leveraging our world-class science and ... Provide strategic leadership for all statistical programming activity related to study, project and submission. Manage CRO to ensure high quality compound and… more
- Daiichi Sankyo, Inc. (Basking Ridge, NJ)
- …in due-diligence activities, and represents global function on study and project teamsProduces independent writing for publications and regulatory ... to improve standards of care and address diversified, unmet medical needs of people globally by leveraging our world-class...support Phase 2/3 studies, represent function on study and project teams, and participate in and contribute to regulatory… more
- Insmed Incorporated (Bridgewater, NJ)
- …Research groups. The role will provide scientific and strategic guidance to global project teams and will oversee the internal and CRO resources as they relate ... to TBS.ResponsibilitiesLead projects , provide oversight of outsourced GxP bioanalytical validations and sample analysis from early to late development for… more
- Daiichi Sankyo, Inc. (Basking Ridge, NJ)
- …pharmaceutical therapies to improve standards of care and address diversified, unmet medical needs of people globally by leveraging our world-class science and ... as main statistical contact for the assigned studies and projects . Provides guidance to study team on all aspects...globally by providing input for the interaction or by writing the interaction document. May participate in meeting or… more
- Daiichi Sankyo, Inc. (Basking Ridge, NJ)
- …and amendments.Lead document review & coordination for the protocol and amendments. Additional medical writing tasks may involve ICF, CRF guidelines, IB and ... pharmaceutical therapies to improve standards of care and address diversified, unmet medical needs of people globally by leveraging our world-class science and… more
- Novo Nordisk Inc. (Durham, NC)
- …the world, driving the stability portfolio for all products, and writing and maintaining regulatory documentation. Relationships Director . Essential Functions ... 100 years, Novo Nordisk has been tackling the unmet medical needs of people living with serious chronic diseases,...successful execution of support to the productions Coordinate with Director , Bulk, Pack, QC & EM & other teams… more
- Jazz Pharmaceuticals (Palo Alto, CA)
- …visit www.jazzpharmaceuticals.com and follow @JazzPharma on Twitter. Brief Description:The Director , Toxicology is accountable for managing the global nonclinical ... of Jazz programs, from research to registration and beyond. The Director , Toxicology, reports to the Head of Toxicology.Essential FunctionsThe eligible candidate… more
- Jazz Pharmaceuticals (Philadelphia, PA)
- …[clinical and medical affairs], data science, regulatory, clinical development, medical writing , and other vital functions and represent Statistical ... visit www.jazzpharmaceuticals.com and follow @JazzPharma on Twitter. Brief Description: The Director will be responsible for managing the product leaders and… more
- Jazz Pharmaceuticals (Philadelphia, PA)
- …[clinical and medical affairs], data science, regulatory, clinical development, medical writing , and other vital functions and represent Statistical ... information, please visit and follow @JazzPharma on Twitter. Brief Description: The Director will be responsible for managing the product leaders and external FSP… more
- UT Health Tyler (Tyler, TX)
- …healthcare, together. POSITION SUMMARY The position of Quality and Patient Safety Director at UTHET is accountable for assisting the organization to improve quality, ... system improvements using quality data, event and regulatory compliance reports. Provides project management to assigned teams by providing leadership to focus areas… more
- Northrop Grumman (Roy, UT)
- …and launch your career today. Northrop Grumman Space Systems is seeking a Project Manager Engineer in support of the Sentinel program. - Northrop Grumman supports ... Systems, you are eligible for our robust benefits package including: - Medical , Dental & Vision coverage 401k Educational Assistance Life Insurance Employee… more
