- Merck & Co. (North Wales, PA)
- …Clinical Trial Team lead. Leads and directs teams in key study planning, development, and execution elements (eg operational reviews, issue escalation/mitigations, ... Responsible for facilitating and collaborating with key internal/external stakeholders ( study team, subsidiary country teams, vendors, committees, etc.) in support… more
- Merck & Co. (North Wales, PA)
- …Material(s):n/aRequired Skills:Adaptability, Adaptability, Clinical Data, Clinical Operations, Clinical Research , Clinical Study Design, Clinical Testing, ... 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. (Rahway, NJ)
- …Leadership, Scientific Publications, Strategic Planning, University Education-Preferred Skills:Clinical Research , Clinical Studies , Clinical Trial Protocols, ... Job DescriptionOur Clinical and Pharmacovigilance teams manage studies to provide the safety and efficacy data required for regulatory approval of potential new… more
- Merck & Co. (Rahway, NJ)
- …has primary responsibility for the planning and directing of clinical research activities involving new or marketed Oncology medicines. Our company Oncology ... will manage the entire cycle of clinical development, including study design, placement, monitoring, analysis, regulatory reporting, and publication.Specifically,… 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 ... of country specific HTA/reimbursement needs for the product and gain input on research design and implementation of retrospective database studies , assessment of… 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 ... DescriptionRole SummaryThe Principal Scientist/Director, Value & Implementation (V&I) Outcomes Research , position resides in the V&I organization, which includes… more
- Merck & Co. (South San Francisco, CA)
- …I studies ; close collaboration with internal and external clinical study support staff and scientists (including discovery research , biostatistics, drug ... Principal Scientist Translational Medicine, Immunology Translational Medicine in our Research & Development Division is responsible for planning and management… more
- Merck & Co. (North Wales, PA)
- …providers, HTAs, patient organizations, and othersTo design and implement outcomes research studies , in collaboration with scientific leaders, patient ... research organizations, database holders, and others.To prepare outcomes research protocols, statistical analysis plans, and clinical study reports.To… more
- Merck & Co. (Chicago, IL)
- …and goals for approved, in-development, and active Company-sponsored trials and/or investigator-sponsored research studies and serve as a role model for other ... scientific/data exchange within our AOI to determine the alignment with our research strategies, studies concepts, scientific merit, and qualifications for a… more
- Merck & Co. (North Wales, PA)
- …and goals for approved, in-development, and active Company-sponsored trials and/or investigator-sponsored research studies . The RMSD serves as a role model for ... scientific/data exchange within our AOI to determine the alignment with our research strategies, studies concepts, scientific merit, and qualifications for a… more
- Merck & Co. (Boston, MA)
- …to the following: conduct TK modeling to support dose-selection on toxicity studies , provide TK study design, calculate PK/TK parameters, interpret results, ... quality scientific results according to agreed timeline for several concurrent studies .Effectively communicate study results at internal meetings, as… more
- Merck & Co. (North Wales, PA)
- …personnel at regulatory agencies and with investigators concerning proposed or ongoing studies .Collaborates in publication of research results in areas of ... position involves interaction with Medical, Data Coordination, Statistical Programming, Research Laboratories scientists and Regulatory staffs in designing and… more
- Merck & Co. (Rahway, NJ)
- …managing the 'end-to-end' integrated clinical supply chain across the full c ompany's Research & Development Division portfolio of clinical trial s .- GCS is ... 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)
- …Skills:Adaptability, Adaptability, Clinical Data, Clinical Operations, Clinical Outcomes, Clinical Research , Clinical Study Design, Clinical Testing, Clinical ... 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)
- …at regulatory agencies and with investigators concerning proposed or ongoing studies .Involved in research activities for innovative statistical methods and ... Job DescriptionIn BARDS (Biostatistics and Research Decision Sciences), a distinguished department within our...results from clinical trials to meet objectives of the study protocol.- Independently applies and implements basic and complex… more
- Merck & Co. (Rahway, NJ)
- …Biological Sciences, Clinical Data, Clinical Data Interpretation, Clinical Operations, Clinical Research , Clinical Study Design, Clinical Testing, Clinical Trial ... Collaborating cross-functionally in the development of Protocol and related study materials (e . g . , ICF documents/...other clinical scientists. Core Skills Solid knowledge of clinical research regulatory requirements (e . g . , GCP… 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 ... leaders and Global Brand leaders. They collaborate with V&I Outcomes Research , Policy and Market Access. Primary Responsibilities:Accountable for the generation of… more
- Tris Pharma (Monmouth Junction, NJ)
- Analytical Research and Development Scientist II Monmouth Junction, NJDepartment: Analytical Research and Development and Characterization / Analytical ... Junction, NJ headquarters has an immediate need for an experienced Analytical Research and Development Scientist IISummaryThe Analytical Research and Development… more
- Merck & Co. (North Wales, PA)
- ….Supervises development of clinical documents including protocols, clinical study reports and background documents.Interfaces with functional experts across ... therapeutic area content expert within the company, providing input into research and business development priorities and prioritization of clinical assets.-May… more
