- Merck & Co. (North Wales, PA)
- …to demonstrate your advanced leadership and technical skills as part of a global , cross-functional team. You will build and coach your team in the development ... Clinical Trial Team lead. Leads and directs teams in key study planning, development, and execution elements (eg operational reviews, issue escalation/mitigations,… more
- Merck & Co. (North Wales, PA)
- …to demonstrate your leadership and technical skills as part of a global , cross-functional team. You will apply project management, communication, and collaboration ... serve as the clinical trial team leadMay lead team in key study planning, development, and execution elements (eg, data management deliverables, trial level… more
- Merck & Co. (North Wales, PA)
- ….Supervises development of clinical documents including protocols, clinical study reports and background documents.Interfaces with functional experts across ... Job DescriptionThe Associate Vice President (AVP)/Section Head, Global Clinical Development, Pediatrics will focus on driving strategy, development, and life-cycle… more
- Merck & Co. (South San Francisco, CA)
- … studies ; close collaboration with internal and external clinical study support staff and scientists (including discovery research, biostatistics, drug ... 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. (North Wales, PA)
- …researchIdentifies barriers to patient enrollment and retention efforts to achieve study milestonesUpon request from Global Clinical Trial Operations ... Work Arrangements:RemoteShift:Valid Driving License:Hazardous Material(s):Required Skills:Clinical Affairs, Clinical Studies , Clinical Trials, Medical Affairs, Medical Relations, Pharmaceutical Medical… more
- Merck & Co. (Rahway, NJ)
- …and programsIn collaboration with internal teams and external partners, designs studies , authors study protocols, develops measurement questionnaires, case ... payers, policymakers, HTA/reimbursement agencies, and health systems globally.Types of studies executed include prospective and retrospective observational studies… more
- Merck & Co. (North Wales, PA)
- …with the Investigator Study Program Committee to evaluate outcomes research study protocols for studies in local markets.Supports affiliates to understand ... and gain input on research design and implementation of retrospective database studies , assessment of patient reported outcomes, epidemiological studies and… more
- Merck & Co. (Chicago, IL)
- …research.Identifies barriers to patient enrollment and retention efforts to achieve study milestones.Upon Request from Global Clinical Trial Operations ... to scientific questions from SLs, including questions about Company products. The work is aligned to Scientific Exchange, Research, Scientific Congress Support, and… more
- Merck & Co. (North Wales, PA)
- …and programs.In collaboration with internal teams and external partners, designs studies ; authors study protocols; and develops measurement questionnaires, case ... (V&I) Outcomes Research, position resides in the V&I organization, which includes Global Medical and Scientific Affairs as well as Outcomes Research, and will… 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… 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 ... Job DescriptionThe Executive Director Pulmonary Hypertension, Value & Implementation (V&I), Global Medical and Scientific Affairs (GMSA) (referred to as EDMA) is… more
- Merck & Co. (Rahway, NJ)
- Job DescriptionThe Global Clinical Supply (GCS) organization is accountable for managing the 'end-to-end' integrated clinical supply chain across the full c ompany's ... for establishing the timelines for clinical supply needs per study and providing the signal for sourcing, manufacturing, packaging,...d evelopment and User Acceptance Testing (UAT) for assigned studies . - Mentors new team members and supports… more
- Merck & Co. (North Wales, PA)
- …leadership, technical skills, and scientific acumen as part of a global , cross functional team.Job ResponsibilitiesResponsible for leading specific aspects of ... include:Collaborating cross-functionally in the development of Protocol and related study materials (eg, ICF documents / amendments); Partners with the… more
- Merck & Co. (Rahway, NJ)
- …your leadership, technical skills, and scientific acumen as part of a global , cross-functional team . - Job Responsibilities - Responsible for leading specific ... responsibilities include: Collaborating cross-functionally in the development of Protocol and related study materials (e . g . , ICF documents/ amendments); Partners… more
- Merck & Co. (Rahway, NJ)
- …of medical drugs and vaccines for the benefit of patients and global human health. Responsibilities :Develops, coordinates, and provides biostatistical support for ... the statistical activities for clinical drug/vaccine projects.The incumbent may initially work in a specific disease therapeutic area. Primary activities :Serves as… 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)
- …of medical drugs and vaccines for the benefit of patients and global human health.The Associate Vice President (AVP), Late Development Statistics, BARDS, is ... support for a number our company's late-stage products in Oncology. The AVP will work under the direction of the Late Development Statistics Vice President in BARDS… more
- Merck & Co. (Rahway, NJ)
- Job DescriptionThe Global Clinical Supply (GCS) organization is accountable for managing the 'end-to-end' integrated clinical supply chain across the full Research & ... the downstream activities of clinical supplies for their assigned studies . -The primary function of the IM CSPM is...Operations etc.) as well as other organizations such as Global Clinical Trial Operations (GCTO) Regional colleagues and … more
- Merck & Co. (Rahway, NJ)
- …medical drugs and vaccines for the benefit of patients and global human health.Responsibilities: The Senior Statistical Programmer, Submission Data Standards Quality ... other project stakeholders. Primary Activities: PreNDA and PreBLA meeting preparation, study data standards plan, preparing questions for FDA e-data mailboxes… more
- Merck & Co. (South San Francisco, CA)
- …of novel therapeutic agents for cardiometabolic and ophthalmologic diseases. You will work on the discovery and development of small molecules, biologics and ... of drug discovery and development. The Associate Director should demonstrate collaborative work spirit and excellent communication skills and should work … more
