- Merck & Co. (South San Francisco, CA)
- …into the earliest stages of target identification and validation, and executing clinical studies to evaluate the relevance of potential targets to human disease in ... strategies through cross-functional teams that provide line-of-sight from First-in-Human studies through clinical Proof-of-Concept.- This includes Experimental Medicine … more
- Merck & Co. (Rahway, NJ)
- Job DescriptionOur Clinical and Pharmacovigilance teams manage studies to provide the safety and efficacy data required for regulatory approval of potential new ... or marketed Neuroscience drugs;Analyzing and summarizing the clinical findings from studies to support decisions regarding safety and efficacy as well as… 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
- 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. (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)
- …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
- 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
- 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
- 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. (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. (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)
- …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)
- …real-world evidence data generation and coordinates local data generation studies with V&I Outcomes ResearchSupports the Investigator-Initiated Study programLeads ... protected characteristics.--As a federal contractor, we comply with all affirmative action requirements for protected veterans and individuals with disabilities.-… more
- Daiichi Sankyo, Inc. (Bernards, NJ)
- …Reports and Common Technical Document submission.ResponsibilitiesSupport audit program for clinical studies and vendors as applicable for the area of GxP audits ... working within early development through Phase III and Pharmacovigilance studies preferredMedical, technical writing experience a plus Travel Ability Must… more
- Merck & Co. (North Wales, PA)
- …in life sciences, preferred.Experience in planning and executing clinical studies in ophthalmology highly preferredAs an Equal Employment Opportunity Employer, ... protected characteristics.--As a federal contractor, we comply with all affirmative action requirements for protected veterans and individuals with disabilities.-… more
- Merck & Co. (Rahway, NJ)
- …analytical problem-solving and optimization, trace impurity quantitation, characterization studies , and cross-functional initiatives. The individual will also drive ... protected characteristics.--As a federal contractor, we comply with all affirmative action requirements for protected veterans and individuals with disabilities.-… more
- 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… more
- Daiichi Sankyo, Inc. (Bernards, NJ)
- …and statistical aspects for safety signal detection and characterization for ongoing studies and compound level pooled clinical trial data of project(s). Act as ... statistician required. Travel: 10%Daiichi Sankyo, Inc. is an equal opportunity/ affirmative action employer. Qualified applicants will receive consideration for… more
- Merck & Co. (Rahway, NJ)
- …Response (IVR) System d evelopment and User Acceptance Testing (UAT) for assigned studies . - Mentors new team members and supports staff development, as needed ... protected characteristics.--As a federal contractor, we comply with all affirmative action requirements for protected veterans and individuals with disabilities.-… more
