- Daiichi Sankyo, Inc. (Bernards, NJ)
- …and employeesExpertise working within early development through Phase III and Pharmacovigilance studies preferred Travel:Must have the ability to travel up to ... 15% domestic and internationalDaiichi Sankyo, Inc. is an equal opportunity/affirmative action employer. Qualified applicants will receive consideration for employment without regard to sex, gender identity, sexual orientation, race, color, religion, national… more
- Merck & Co. (South San Francisco, CA)
- …as well as independent academic research for a position in our group.The preferred candidate will have at least 5-year experience in the pharmaceutical industry and ... into the earliest stages of target identification and validation, and executing clinical studies to evaluate the relevance of potential targets to human disease in… more
- Merck & Co. (Rahway, NJ)
- …Scientific Leadership, Scientific Publications, Strategic Planning, University Education- Preferred Skills:Clinical Research, Clinical Studies , Clinical ... Job DescriptionOur Clinical and Pharmacovigilance teams manage studies to provide the safety and efficacy data required for regulatory approval of potential new… more
- Aequor (MA)
- …to support the identification of therapeutic candidates from discovery into IND enabling studies . Execute studies to generate proof of concept data. Apply ... identify therapeutic candidates. Demonstrate scientific excellence, initiate, design, and execute experiments/ studies in support of goals in a time sensitive manner.… more
- Merck & Co. (North Wales, PA)
- …Evidence (RWE) in Oncology.- -Position objectivesTo design and execute real-world evidence studies , designed to demonstrate the value of new products in support of ... inform and contribute to the value evidence plan and associated studies which demonstrate clinical, economic, and patient-centered value. The work will… more
- Daiichi Sankyo, Inc. (Bernards, NJ)
- …Support as medical lead for select company-sponsored GMA evidence generating studies /projects. Manages all medical aspects such as study document development and ... other cross-functional and regional stakeholders.- Provides support in review of investigator-initiated studies (IIS) and may serve as deputy compound lead in Global… more
- Merck & Co. (Boston, MA)
- …executing all phases/aspects of toxicokinetics support of nonclinical toxicity studies [ie, exploratory and definitive/Good Laboratory Practice (GLP)], serving as ... a contributing scientist/principal investigator on toxicity studies , and executing PK/TK strategies to support the development of small molecules and biologics.The… more
- BioAgilytix (Durham, NC)
- …(BPM)/Principal Investigator (PI), overseeing all aspects of bioanalytical studies -including project scope definition, proposal preparation, timelines, scheduling, ... Manager (BPM)/Principal Investigator (PI), overseeing all aspects of bioanalytical studies including project scope definition, proposal preparation, timelines, scheduling,… more
- Merck & Co. (Chicago, IL)
- …for approved, in-development, and active Company-sponsored trials and/or investigator-sponsored research studies and serve as a role model for other field medical ... within our AOI to determine the alignment with our research strategies, studies concepts, scientific merit, and qualifications for a specific compound or… more
- Merck & Co. (North Wales, PA)
- …and gain input on research design and implementation of retrospective database studies , assessment of patient reported outcomes, epidemiological studies and ... Study Program Committee to evaluate outcomes research study protocols for studies in local markets.Supports affiliates to understand local needs, adapt health… more
- Merck & Co. (Rahway, NJ)
- …for small, intermediate, and large molecules from preclinical toxicology studies to commercialization. -Our development teams ensure robust composition, primary ... tools to drug product development, and experience in designing appropriate DOE studies to inform on risks.Experience with process scale-up, definition of critical… more
- Merck & Co. (North Wales, PA)
- …for approved, in-development, and active Company-sponsored trials and/or investigator-sponsored research studies . The RMSD serves as a role model for other field ... within our AOI to determine the alignment with our research strategies, studies concepts, scientific merit, and qualifications for a specific compound or… more
- Eisai, Inc (Nutley, NJ)
- …as well as the clinical execution and oversight of the associated studies being conducted globally. The Executive Director will champion transformational business ... bodies in order to conduct Phase I, Phase II and Phase III studies , and prepare related documentation for submissions.This position will lead a development team… more
- Merck & Co. (Rahway, NJ)
- …policymakers, HTA/reimbursement agencies, and health systems globally.Types of studies executed include prospective and retrospective observational studies ... programsIn collaboration with internal teams and external partners, designs studies , authors study protocols, develops measurement questionnaires, case report forms,… more
- Merck & Co. (North Wales, PA)
- …assessment (HTA)/reimbursement agencies and health systems globally.Types of studies executed include prospective and retrospective observational studies ... programs.In collaboration with internal teams and external partners, designs studies ; authors study protocols; and develops measurement questionnaires, case report… more
- BioAgilytix (San Diego, CA)
- …scientific and operational activities in support of preclinical, clinical, and product release studies for our San Diego lab. This role requires deep expertise in ... bioanalytical assays for support of preclinical, clinical and product release studies .Motivating team by inspiring employees to achieve goals and aligning employee… more
- Eisai, Inc (Nutley, NJ)
- …execution within a pharmaceutical or biotechnology company. This role ensures studies are conducted efficiently, within budget, and in compliance with regulatory ... activities directly impact the timeliness, quality, and successful execution of clinical studies in accordance with the overarching project plans established by the… more
- Merck & Co. (Rahway, NJ)
- …plans associated with the downstream activities of clinical supplies for their assigned studies . -The primary function of the IM CSPM is planning the availability of ... key technological tools in the planning and managing of clinical supplies for assigned studies such as IRT & Microsoft PowerApps. -Works directly in the SAP system… more
- Merck & Co. (Rahway, NJ)
- …investigational or marketed Oncology drugsAnalyzing and summarizing the clinical findings from studies to support decisions regarding safety and efficacy as well as ... in ensuring that appropriate corporate personnel are informed of the progress of studies of our companies and competitors' drugs and internal and external expert… more
- Merck & Co. (Rahway, NJ)
- …real-world evidence data generation and coordinates local data generation studies with V&I Outcomes ResearchSupports the Investigator-Initiated Study programLeads ... R&D V&I GMSAEducation: MD, Ph.D., DDS/DMD or Pharm.D. (MD strongly preferred ) and recognized medical expertise -Required Experience and Skills:TA specialization as… more
