- Merck & Co. (Rahway, NJ)
- …the further study of marketed compounds.In executing these duties, the Director may:Supervise the activities of Clinical Scientists in the execution of clinical ... talented and dedicated colleagues while developing and expanding your career.--The Director (Principal Scientist) has primary responsibility for the planning and… more
- Daiichi Sankyo, Inc. (Bernards, NJ)
- …for managing the multiple Clinical Science Asset Leaders (CSALs) at the Senior Director level for each respective program. This Clinical Science (CS) Group Lead will ... site scientific engagement, and HA responses. Interactions with the internal clinical study physicians and physician scientists as well as external investigators is… more
- Daiichi Sankyo, Inc. (Bernards, NJ)
- …for select company-sponsored GMA evidence generating studies /projects. Manages all medical aspects such as study document development and drives execution ... other research areas centered around rare diseases and immune disorders. Summary The Director Global Medical Affairs Oncology (GMA), ADC, under the direction of… more
- Daiichi Sankyo, Inc. (Bernards, NJ)
- …to relevant internal stakeholders using trackers and tools generated by Global Oncology Medical Affairs Study Operations partners and propose mitigation ... other research areas centered around rare diseases and immune disorders. SummaryThe Director , Global Oncology Medical Affairs, Evidence Generation role is… more
- Daiichi Sankyo, Inc. (Bernards, NJ)
- …to relevant internal stakeholders using trackers and tools generated by Global Oncology Medical Affairs Study Operations partners and propose mitigation ... other research areas centered around rare diseases and immune disorders.SummaryThe Senior Director , Global Oncology Medical Affairs, Evidence Generation role is… more
- Novo Nordisk Inc. (Plainsboro, NJ)
- …Trial Strategy Team in collaboration with Clinical Operations point, Clinical Director , and Field Medical Affairs point to identify investigators/sites and ... you ready to make a difference? The Position The Medical Director serves as the subject matter...Inc. and Global HQ. Key internal relationships include Field Medical Affairs, Medical Strategy & Operations… more
- Daiichi Sankyo, Inc. (Bernards, 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 other research areas centered around rare diseases and immune disorders. Director , Diagnostic Sciences Global Companion Diagnostics Job Summary The Director… more
- Daiichi Sankyo, Inc. (Bernards, 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… more
- Daiichi Sankyo, Inc. (Bernards, NJ)
- …level. Reviews and oversee completion of clinical trial protocols. Provides medical and/or scientific direction to Clinical Operations . Represents Clinical ... 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. (Bernards, NJ)
- …regulatory requirements. This position has advanced experience working on Phase I-IV studies within the medical device and/or pharmaceutical industry across ... 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. (Bernards, NJ)
- …and control of Clinical Project Budget in support of Phase I-III clinical studies . Partner with Project Management, Clinical Operations and other functional ... to improve standards of care and address diversified, unmet medical needs of people globally by leveraging our world-class...and control of functional budget in support of global operations of RD unit. Partner with global function leaders… more
- Tris Pharma (Monmouth Junction, NJ)
- …of Good Clinical Practices (GCPs). The role partners with Clinical Development, Clinical Operations , Medical Affairs and R&D Quality Assurance to develop and ... Junction, New Jersey, Tris has an immediate opening for a full-time permanent Director /Senior Director , Clinical Quality Assurance. This is a hybrid position.… more
- Novo Nordisk Inc. (Plainsboro, NJ)
- …into development plans, study designs, and regulatory submissions. Relationships The Principal Medical Writer reports to a Director of Medical Writing. ... Medical Writer will work closely with cross-functional project teams, including Medical & Science, Clinical Operations , Biometrics, and Regulatory Affairs… more
- Novo Nordisk Inc. (Plainsboro, NJ)
- …and local cross-functional study teams, including personnel from Medical & Science, Clinical Pharmacology, Biostatistics, Clinical Operations , Regulatory ... the clinical development and regulatory requirements of a clinical program. Relationships The Senior Medical Writer reports to a Director of Medical Writing.… more
- Daiichi Sankyo, Inc. (Bernards, NJ)
- …pharmaceutical therapies to improve standards of care and address diversified, unmet medical needs of people globally by leveraging our world-class science and ... privacy, legal, compliance, IT security, etc.Responsibilities- In conjunction with the Director of Data Stewardship, Cataloging and Process, develop implement a data… more
- Regeneron Pharmaceuticals (Sleepy Hollow, NY)
- The Director , Medical Study Operations will oversee several of our External Sponsored Research (ESR) programs inclusive of Investigator-Initiated ... Studies (IIS) and Research Collaboration (RC). Responsibilities will also...regulatory or field-based function in pharmaceutical industry. Experience in Medical Study Operations is required.… more
- Gilead Sciences, Inc. (Parsippany, NJ)
- …create possible, together. **Job Description** We are seeking a strong, experienced Clinical Operations leader for a Director position within our Oncology Lung ... be responsible for the successful execution of more complex studies and/or multiple studies within a program...an effort to streamline timelines without compromise to quality study deliverables. + Acts as the Clinical Operations… more
- Mitsubishi Chemical Group (Jersey City, NJ)
- …in creating and implementing experimental medicine studies . Reporting into the Senior Director of the Medical Science Early-Stage, the Director , MSES ... evidence, and creating hope for all facing illness. The Director , Medical Science MSES, will be primarily...Development studies from Phase 0 through Proof-of-Concept studies . In this role, the Director , MSES,… more
- AbbVie (Florham Park, NJ)
- …(AE's) and Serious Adverse Events (SAE's) if assigned to AbbVie conduct on clinical studies . Qualifications Medical Director Qualifications + Medical ... overall scientific strategy. + Has overall responsibility for oversight of clinical studies , monitoring overall study integrity and review, interpretation and… more
- Mitsubishi Chemical Group (Jersey City, NJ)
- …scientific aspects of translational studies from Phase 0 through Proof-of-Concept studies . In this role, the Director , TM, will contribute to accelerating ... is highly desirable. + Experience in analyzing and presenting results of clinical studies to senior leadership/ KOLs/ medical communities and regulatory agencies… more
