- Eisai, Inc (WA)
- …Job Description Summary We are seeking a visionary leader to shape and drive Clinical Data Science strategy across our global clinical development portfolio. ... role ensures the rigorous application of statistical principles and advanced data science methodologies to optimize clinical trial efficiency and accelerate… more
- Insmed Incorporated (NJ)
- …future of science , we're in. Are you?About the Role:The Global Regulatory Lead (GRL) will be responsible for formulating and implementing global regulatory ... credentials and experience.What You'll Do: Lead development and execution of global regulatory strategies for clinical , pre- clinical , and lifecycle… more
- Insmed Incorporated (NJ)
- …contributions to meaningful progress. That commitment has earned us recognition as Science magazine's No. 1 Top Employer for five consecutive years, certification as ... patients, for each other, and for the future of science , we're in. Are you?About the Role:We're looking for...in. Are you?About the Role:We're looking for a Manager, Regulatory Affairs, Tactical Implementation, on the Regulatory … 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
- Insmed Incorporated (NJ)
- …submission trackers, and regulatory archives.Partner with cross-functional teams ( Regulatory Affairs, CMC, Clinical , Quality) to facilitate document ... meaningful progress. That commitment has earned us recognition as Science magazine's No. 1 Top Employer for five consecutive...in. Are you?About the Role:We're looking for an Associate, Regulatory Operations on the Regulatory team to… more
- Eisai, Inc (Nutley, NJ)
- …difference. If this is your profile, we want to hear from you. The Medical Science Liaison (MSL or Sr. MSL) is a field-facing representative of US Medical Affairs ... the company and its hhc mission; b) provide key scientific and clinical information about Eisai's products/pipeline; serve as a conduit for communication between… more
- Legend Biotech USA, Inc. (Atlanta, GA)
- …an immunotherapy in the treatment of multiple myeloma.Legend Biotech is seeking Medical Science Liaison as part of the Medical Affairs team based in Southeast ... GA). Role OverviewAs part of the US Medical Affairs team, the Medical Science Liaison (MSL) will be responsible for engaging identified key opinion leaders (KOLs)… more
- Larimar Therapeutics (Philadelphia, PA)
- …management team, employees, and consultants have significant expertise in discovery, non- clinical and clinical development, regulatory affairs, manufacturing ... for a company where urgency, agility, and commitment to science win the day - we welcome you! Position... Affairs will be a key member of the regulatory , clinical project, and technical operations (cross-functional)… more
- Eisai, Inc (Ann Arbor, MI)
- …international regulatory /ethical guidelines relevant to the pharmaceutical industry & clinical trial conduct, and to ensure compliance with these external as ... with strategic and tactical planning, working collaboratively with Medical Affairs and Clinical Development teams for support of clinical studies across the… more
- Merck & Co. (Rahway, NJ)
- …Respect - Inclusion.Design and organization of paper and Electronic Data Capture (EDC) clinical studies that meet scientific and regulatory requirements by the ... Sciences, Clinical Site Management, Clinical Study Design, Clinical Trials Operations, Computer Science , Design, Detail-Oriented, Ethical Compliance,… more
- Insmed Incorporated (NJ)
- …clinical studies, reviewing & interpreting clinical trial data, authoring clinical study and regulatory communications and documents, and monitoring of ... clinical development team, partnering closely with heads of clinical operations, toxicology, regulatory affairs, commercial, pharmacovigilance, clinical… more
- Merck & Co. (Upper Gwynedd, PA)
- … development, including study design, placement, monitoring, analysis, regulatory reporting, and publication. -- Responsibilities: Specifically, the Senior ... --Work closely with a cross-functional group of experts in commercialization, regulatory affairs, statistics, and manufacturing to manage clinical development… more
- Insmed Incorporated (San Diego, CA)
- …functional teams. You will provide clinical and scientific support to clinical development and operations, regulatory , medical affairs, drug safety, and ... meaningful progress. That commitment has earned us recognition as Science magazine's No. 1 Top Employer for five consecutive...in. Are you?About the Role:We're looking for a Director, Clinical Scientist for the Gene Therapy Clinical … more
- Insmed Incorporated (NJ)
- …maintenance, to ensure robust supply tracking and randomization supportCollaborate with CMC, Clinical Ops, Quality, Regulatory , and Commercial Supply teams to ... a high performing team across all levelsExperience in multi-functional areas ( Clinical , Regulatory , Quality) demonstrating a broad understanding of… more
- Insmed Incorporated (NJ)
- …contributions to meaningful progress. That commitment has earned us recognition as Science magazine's No. 1 Top Employer for five consecutive years, certification as ... patients, for each other, and for the future of science , we're in. Are you?About the Role:Accountable for providing...budget and with high quality. This role may manage clinical operations team members, as delegated by supervisor, to… more
- Genmab (NJ)
- …compassionate, candid, and purposeful, and our business is innovative and rooted in science . We believe that being proudly authentic and determined to be our best ... Then we would love to have you join us!The RoleThe Senior Manager, Clinical Programming is responsible for the establishment, governance, and integrity of Study Data… more
- Daiichi Sankyo, Inc. (Bernards, NJ)
- …a key member of the Global Product Team in collaboration with Clinical Development, Regulatory , Project Management, Biostatistics, Pharmacology, and other ... medical needs of people globally by leveraging our world-class science and technology. With more than 125 years of...rare diseases and immune disorders. Summary: The Senior Director, Clinical Safety, will lead the development and implementation of… more
- Eisai, Inc (Nutley, NJ)
- … Pharmacology data as it relates to safety and efficacy.Contributes to Clinical Pharmacology expertise and content to regulatory documents (eg briefing ... a Clinical Pharmacology Project Lead.A thorough understanding of global regulatory requirements on the Clinical Pharmacology and Translational Medicine… more
- Insmed Incorporated (NJ)
- …the clinical study startup processes such as demand forecasting, regulatory submissions, and vendor/contract management.Coordinate with the Clinical Supply ... meaningful progress. That commitment has earned us recognition as Science magazine's No. 1 Top Employer for four consecutive...About the Role:We're looking for a Summer Intern - Clinical Supply Chain & Logistics on the Logistics to… more
- Canfield Scientific, Inc (Parsippany, NJ)
- …a multidisciplinary team and engagement in medical writing that drives innovation in clinical science , with the opportunity to further develop their expertise ... for candidates experienced in qualitative health research, patient-reported outcomes, or clinical communication rather than bench science . Job Description:… more
