- Merck & Co. (North Wales, PA)
- …serve as the clinical trial team leadMay lead team in key study planning, development, and execution elements (eg, data management deliverables, trial level ... investigator-meeting planning, communication plans, preparation of status update reports, study close out activities).Leads team for timeline management, risk… more
- Merck & Co. (North Wales, PA)
- …and programsIn collaboration with internal teams and external partners, designs studies , authors study protocols, develops measurement questionnaires, case ... lead cross-functional teams is a critical part of this role.Types of studies executed include prospective and retrospective observational studies to characterize… 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. (North Wales, PA)
- …and programs.In collaboration with internal teams and external partners, designs studies ; authors study protocols; and develops measurement questionnaires, case ... technology assessment (HTA)/reimbursement agencies and health systems globally.Types of studies executed include prospective and retrospective observational studies… 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. (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. (Rahway, NJ)
- …and accountable for establishing the timelines for clinical supply needs per study and providing the signal for sourcing, manufacturing, packaging, and distribution- ... to establish a consolidated , visible forecast for all study product needs (Bulk Drug Product and Clinical Finished...d evelopment and User Acceptance Testing (UAT) for assigned studies . - Mentors new team members and supports… more
- Merck & Co. (Upper Gwynedd, PA)
- Job DescriptionOur Clinical and Pharmacovigilance teams manage studies to provide the safety and efficacy data required for regulatory approval of potential new ... will manage the entire cycle of clinical development, including study design, initiation, execution,- monitoring, analysis, regulatory reporting, publication, and… more
- Merck & Co. (Rahway, NJ)
- … 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
- BioAgilytix (San Diego, CA)
- …assess analytical results, troubleshoot issues, and ensure timely completion of studies .Serve as Principal Investigator or Study Director for GLP/validation ... bioanalytical leader with a strong background in GLP-regulated LC-MS/MS studies to direct our Bioanalytical Chemistry and Formulation Chemistry departments.… more
- Merck & Co. (Rahway, NJ)
- …will manage the entire cycle of clinical development, including study design, placement, monitoring, analysis, regulatory reporting, and publication.Specifically, ... investigational or marketed Oncology drugsAnalyzing and summarizing the clinical findings from studies to support decisions regarding safety and efficacy as well as… more
- Merck & Co. (Rahway, NJ)
- …responsibilities include: Collaborating cross-functionally in the development of Protocol and related study materials (e . g . , ICF documents/ amendments); Partners ... with the Study Manager on study deliverables. Ensuring CRF...benefits (for employee and family), retirement benefits, including 401(k), paid holidays, vacation, and compassionate and sick days. More… more
- Merck & Co. (North Wales, PA)
- …Is involved in late clinical development planning (LDP) to ensure that study designs are consistent with program objectives and meet worldwide regulatory and ... data and interprets results from experiments to meet objectives of the study protocol.- Independently applies and implements basic and complex techniques to these… 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)
- …and interprets results from clinical trials to meet objectives of the study protocol.- Independently applies and implements basic and complex techniques to these ... regulatory agencies, or individual investigators.Provides responses to queries relating to study design, analysis, and interpretation posed by the clinical monitors,… 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
- Johnson Controls (Wichita, KS)
- …What do we offer : Competitive salary Paid vacation/holidays/sick time Comprehensive benefits package including 401K, ... production processes. The industrial engineer's responsibilities include performing time studies , analyzing operations for opportunities for improvement, designing workflows… 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 ... insurance benefits (for employee and family), retirement benefits, including 401(k), paid holidays, vacation, and compassionate and sick days. More information about… more
- Merck & Co. (Rahway, NJ)
- …therapeutic area and encourages appropriate application of new methods to HEOR studies .Maintains responsibility to ensure study conduct is aligned with company ... by their team. These include prospective and retrospective observational studies to characterize disease burden and epidemiology, treatment patterns, health-care… more
