• Legend Biotech USA, Inc. (Raritan, NJ)
    …of an immunotherapy in the treatment of multiple myeloma.Legend Biotech is seeking an Investigator I or Investigator II as part of the Technical Operations team ... based in Raritan, NJ. Role OverviewThe Investigator will be part of Technical Operations team and...in accordance with our company regulations and other global health authority regulators such as FDA. Will collaborate cross… more
    HireLifeScience (10/12/24)
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  • Merck & Co. (Rahway, NJ)
    …GMP regulated environmentExperience working for a health authority/board of health as an inspector, investigator , product reviewer, compliance officer, or ... The responsibility of this position crosses all Human & Animal Health operating units and requires extensive collaboration with manufacturing sites and… more
    HireLifeScience (11/01/24)
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  • Merck & Co. (Rahway, NJ)
    …and to improve outcomes for patients.The EDSA leads a large investigator -initiated studies program in partnership with late-stage development teams in Medical ... and producing comprehensive Congress summary reports.Primary Responsibilities:Leads our Company's Investigator Initiated Studies program for our cardiovascular portfolio (Atherosclerosis,… more
    HireLifeScience (10/30/24)
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  • Merck & Co. (San Francisco, CA)
    …for approved, in-development, and active Company-sponsored trials and/or investigator -sponsored research studies. The Regional Medical Scientific Director serves ... the comprehension of the scientific foundations and goals of investigator -sponsored research.Identifies barriers to patient enrollment and retention efforts to… more
    HireLifeScience (10/25/24)
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  • Eisai, Inc (Nutley, NJ)
    …healthcare provides to patients, their families, and caregivers is Eisai's human health care (hhc) mission. We're a growing pharmaceutical company that is breaking ... certifications and maintain statuses of study team members Assist with investigator meeting planning, including entering clinical meetings into Eisai internal… more
    HireLifeScience (10/17/24)
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  • Novo Nordisk Inc. (Plainsboro, NJ)
    …of both worlds to develop new medicines for patients. We recognize that improving human health starts here and that patients rely on us. We're changing lives for a ... Development Plan (PDP), Trial Outline, Protocol, Clinical Trial Report, Investigator 's Brochure (IB), integrated safety summaries, abstracts and planned publications… more
    HireLifeScience (10/16/24)
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  • Novo Nordisk Inc. (Plainsboro, NJ)
    …most diverse and collaborative groups within the organization. From health -care-provider interactions and developing and implementing regulatory strategies with the ... of investigators for clinical studies and provide medical support to investigator meetings Provide protocol training, disease specific training and titration… more
    HireLifeScience (10/09/24)
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  • Novo Nordisk Inc. (Plainsboro, NJ)
    …most diverse and collaborative groups within the organization. From health -care-provider interactions and developing and implementing regulatory strategies with the ... outlines/protocols for Novo Nordisk-sponsored clinical trials Review proposals for investigator -sponsored studies (ISS) and provide comments to RGC Chair Attend… more
    HireLifeScience (09/20/24)
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  • Novo Nordisk Inc. (Plainsboro, NJ)
    …research across multiple modalities and therapeutic areas. We recognize that improving human health starts here and that patients rely on us. Our R&D hub merges ... Development Plan (PDP), Trial Outline, Protocol, Clinical Trial Report, Investigator 's Brochure (IB), integrated safety summaries, abstracts and planned publications… more
    HireLifeScience (09/13/24)
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  • Novo Nordisk Inc. (Plainsboro, NJ)
    …most diverse and collaborative groups within the organization. From health -care-provider interactions and developing and implementing regulatory strategies with the ... Development (NACD) Clinical Research Equity (CRE) strategy integrating diversity and health equity systematically in clinical trial planning and execution. This role… more
    HireLifeScience (10/31/24)
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  • Daiichi Sankyo, Inc. (Bernards, NJ)
    …personnel as neededStudy-specific subject matter expert (SME) for internal audit or Health Authority (HA) questions related to medical monitoringFor studies in which ... generation/revision; clinical benefit-risk assessments for license renewals, responses to Health Authority)Participant and voting member in the labeling development… more
    HireLifeScience (10/18/24)
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  • Daiichi Sankyo, Inc. (Bernards, NJ)
    …as needed- Study-specific subject matter expert (ME) for internal audit or Health Authority (HA) questions related to medical monitoring- For studies in which ... generation/revision; clinical benefit-risk assessments for license renewals, responses to Health Authority)- Participant and voting member in the labeling… more
    HireLifeScience (09/24/24)
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  • Daiichi Sankyo, Inc. (Bernards, NJ)
    …personnel as neededStudy-specific subject matter expert (ME) for internal audit or Health Authority (HA) questions related to medical monitoringFor studies in which ... generation/revision; clinical benefit-risk assessments for license renewals, responses to Health Authority)Participant and voting member in the labeling development… more
    HireLifeScience (09/24/24)
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  • Merck & Co. (North Wales, PA)
    …is an opportunity to work at the forefront of research to deliver innovative health solutions that advance the prevention and treatment of diseases in people and ... Start up, Data Management, Pharmacovigilance, Essential Document Management, and Investigator / Study Coordinator roles/ responsibilities.-Experience with critical clinical systems… more
    HireLifeScience (10/23/24)
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  • Daiichi Sankyo, Inc. (Boston, MA)
    …and study committee members for DSI clinical research programs, 2) investigator -initiated research study proposals, 3) speakers for DSI Brand Speaker programs, ... college or university)PharmD, MD, PhD or NP in a health sciences-related field or an equivalent combination of education...We are proud of our longstanding commitment to the health and well-being of our employees and their families.… more
    HireLifeScience (09/24/24)
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  • Merck & Co. (Rahway, NJ)
    …final approval of Worldwide Marketing Applications, Clinical Study Reports, protocols, Investigator Brochures before release from our company to external agencies ... $285,800.00Available benefits include bonus eligibility, long term incentive if applicable, health care and other insurance benefits (for employee and family),… more
    HireLifeScience (10/31/24)
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  • Merck & Co. (Rahway, NJ)
    …approval Worldwide Marketing Applications, Clinical Study Reports, protocols, Confidential Investigator Brochures before release from our company to external ... $259,400.00Available benefits include bonus eligibility, long term incentive if applicable, health care and other insurance benefits (for employee and family),… more
    HireLifeScience (10/31/24)
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  • Insmed Incorporated (San Diego, CA)
    …team.Supporting or preparing data interpretation and clinical trial reports.Preparing Investigator Alert letters and SAE reports in collaboration with Clinical ... dependent careAccident and Hospital Indemnity insuranceEmployee Assistance Program (EAP)Mental Health on-line digital resourceWell-being reimbursementPaid leave benefits for new… more
    HireLifeScience (10/30/24)
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  • Novo Nordisk Inc. (Plainsboro, NJ)
    …of both worlds to develop new medicines for patients. We recognize that improving human health starts here and that patients rely on us. We're changing lives for a ... ensure timely and high-quality regulatory deliverables to the GPTs Lead health authority interactions, including leading team through creation of briefing materials… more
    HireLifeScience (09/17/24)
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  • Dana-Farber Cancer Institute (South Boston, MA)
    …patients of all backgrounds, and design programs to promote public health particularly among high-risk and underserved populations. We conduct groundbreaking ... funds, grant balances and charges, ensuring appropriate use of funds under investigator control, both in terms of sponsor/external regulations and Institute policy.… more
    JobGet (11/02/24)
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