Regulatory Affairs Jobs in Rahway, NJ

Job DescriptionThe Clinical Director (Principal Scientist) has primary responsibility for the strategic planning and directing clinical research activities involving investigational compounds in Immunology. With a focus on late-stage development the Clinical Director will manage the entire cycle of...

Job DescriptionThe Clinical and Regulatory Strategic Communications (CRSC) department within GCTO creates and delivers high-quality regulated content in support of our development pipeline and enables data sharing for our customers. We are a strategic partner that ensures excellence and compliance w...

Job DescriptionOur market access team is passionate about bringing our medicines to patients around the world.As a member of the Sac-TMT/Womens Cancers team the Director Oncology Global Market Access will lead global access strategy development and execution for defined Sac-TMT indications within th...

Job DescriptionThe Senior Director (Sr. Principal Scientist) has primary responsibility for the planning and directing clinical research activities involving new or marketed Oncology medicines. Our Companys Oncology medicines span all phases of clinical development (pre-clinical to post-licensure)....

Job DescriptionNorth American GMP Operations Rahway NJWe invite individuals who possess a deep passion for promoting lifesaving and life-enhancing products to join our dynamic team. Our team is highly dedicated and committed to offering exceptional scientific oversight driving the success of our Com...

Job DescriptionThe Senior Director (Sr. Principal Scientist) has primary responsibility for the planning and directing clinical research activities involving new or marketed medicines in the Atherosclerosis section of the Atherosclerosis & Metabolism therapeutic area. Our companys Atherosclerosis &...

Job DescriptionThe Senior Director (Sr. Principal Scientist) has primary responsibility for the planning and directing of clinical research activities involving new or marketed Oncology medicines. Our Companys Oncology medicines span all phases of clinical development (pre-clinical to post-licensure...

Job DescriptionWe invite you to join our mission of advancing the prevention and treatment of diseases. The purpose of Global Labeling is to drive labeling strategy and ensure high-quality and compliant labeling documents which provide the safe and effective use of products for patients and healthca...

Job DescriptionThe Associate Director is responsible for the review and approval of all US promotional materials and serving as the promotional regulatory expert with legal medical and commercial colleagues to ensure that promotional practices are consistent with regulatory guidelines our Companys p...

Job DescriptionReporting to the Head of Statistical Programming (SP) the Executive Director leads a team of statistical programmers and analysts supporting foundational analysis and reporting tools including standard code libraries platforms processes training and the generation and management of cl...

Job DescriptionJob SummaryThe Clinical Director (Principal Scientist) has primary responsibility for planning and directing clinical research activities involving new or marketed medicines in the ophthalmology therapeutic area. Our companys ophthalmology medicines span all phases of clinical develop...

Job DescriptionThe Associate Vice President (AVP) has primary responsibility for the planning and directing clinical research activities involving new or marketed drugs for oncology indications. The Associate Vice President will manage and oversee the entire cycle of clinical development including s...

Job DescriptionThe Distinguished Scientist/ Executive Director within Companion Diagnostics (CDx) Development will lead one of our companys Diagnostic Development Teams (DxDTs) supervising PhD-/MD-level employees developing and overseeing CDx strategy development alignment and execution for specific...

Some careers open more doors than others.If youre looking for a career that will unlock new opportunities join HSBC and experience the possibilities. Whether you want a career that could take you to the top or simply take you in an exciting new direction HSBC offers opportunities support and rewards...

Job DescriptionWe are seeking a highly experienced and skilled Senior Glass and Critical Component Technical Expert to join our team as a key technical support resource for our pharmaceutical and combination product engineering projects. The ideal candidate will have extensive knowledge and expertis...

Job DescriptionRole Summary The Senior Specialist Global Medical Information is an entry-level headquarters (HQ)-based role within V&I Global Medical and Scientific Affairs (GMSA) responsible for the US and global core functions of the GMI organization: Medical Information which includes handling of...

Job DescriptionGlobal Project and Alliance Management (GPAM) is part of the Research and Development organization at our Company which is also referred to as our Companys Research Laboratories.The Integrated Project Planning (IPP) group within GPAM partners with Project Managers to advance the pipel...

Job DescriptionOur Global Oncology team is dedicated to delivering breakthrough innovations that extend and improve the lives of cancer patients worldwide. Our team of forward-thinking individuals achieves this through an unwavering commitment to support accessibility to medicine providing new thera...

Job DescriptionDepartmentRegulatory Planning and Publishing (RPP)Brief Description of PositionThe Associate Specialist of Regulatory Planning & Publishing works closely with various stakeholders of regulatory and safety submissions to assist in activities related to planning execution and management...

Job DescriptionJoin Our Companys Rahway Animal Health TeamOur Companys Global Animal Health Research & Development (R&D) division is a pioneer in the discovery development and registration of medicines products and therapeutics for animals. To strengthen the team responsible for our global initiativ...