- Merck & Co. (Rahway, NJ)
- …Practice (GLP) studies .The Associate Principal Scientist is the primary clinical study team leader and has overall responsibility for a study .The Associate ... function is to design, coordinate, monitor, and report clinical laboratory and field studies that will support the regulatory approval of new companion animal and… more
- Merck & Co. (North Wales, PA)
- …may: Supervise the activities of Clinical Scientists in the execution of clinical studies . -- Work closely with a cross-functional group of experts in ... will manage the entire cycle of clinical development, including study design, placement, monitoring, analysis, regulatory reporting, and publication. --Specifically,… more
- Merck & Co. (New York, NY)
- …to scientific questions from SLs, including questions about company products - The work of a Regional Medical Scientific Director is aligned to: Scientific Exchange, ... approved, in-development, and active company-sponsored trials and/or investigator-sponsored research studies - The Regional Medical Scientific Director serves as a… more
- Merck & Co. (North Wales, PA)
- …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. (South San Francisco, CA)
- …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. (Rahway, NJ)
- …will manage the entire cycle of late-stage clinical development and studies , including development strategy, study design, initiation, execution, monitoring, ... May: Supervise the activities of Clinical Scientists in the execution of clinical studies . Work closely with a cross-functional group of experts in… more
- Merck & Co. (Rahway, NJ)
- …the statistical activities for clinical drug/vaccine projects.The incumbent may initially work in a specific disease therapeutic area. Primary activities :Serves as ... and interprets results from clinical trials to meet objectives of the study protocol.- Independently applies and implements basic and complex techniques to these… more
- Merck & Co. (Rahway, NJ)
- …plans for all activities associated with clinical supplies for their assigned studies , which could vary in complexity. This individual serves as the primary ... 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. (Boston, MA)
- …may supervise the activities of Clinical Scientists in the execution of clinical studies . Work closely with a cross-functional group of experts in ... the Executive Director may be responsible for:Evaluating pre-clinical and translational work for the purpose of generating early clinical development plans and… more
- Merck & Co. (Rahway, NJ)
- …of COA endpoints to support overall product development. The Senior Scientist will work closely with the PaCES lead to collaborate with individuals from Clinical ... the PaCES lead to provide guidance on implementing COA/PRO instruments into studies by following our Company's standard processesAttend Clinical Trial Team (CTT)… more
- Merck & Co. (San Diego, CA)
- …successful candidate will lead projects from discovery to start of IND-enabling studies , with focus on antibodies, bispecific molecules, and evaluation of novel ... analyze new cellular and molecular assays to support mechanism-of-action studies for therapeutic candidate progression.Hands-on development of experiments related… more
- Merck & Co. (Boston, MA)
- …insights /expert advice regarding tumor specific development; will design and conduct basket studies for assets; will work with Early Oncology to advance ... of development across different disease TA sections, timing of studies across Disease Therapeutic Areas (TA) and timing of...and timing of launches. The Vice President (VP) will work collaboratively with Oncology VP TA heads directly 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. (Rahway, NJ)
- …for small, intermediate, and large molecules from preclinical toxicology studies to commercialization. Our development teams ensure robust composition, primary ... and patents.The candidate should have experience in designing and executing appropriate DOE studies to inform on biologic drug product risks such as oxidation or… more
- Merck & Co. (Rahway, NJ)
- …other project stakeholders. Primary Activities: PreNDA and PreBLA meeting preparation, study data standards plan, preparing questions for FDA e-data mailboxes ... assuring consistency across protocols and projectsAbility and interest to work across cultures and geographiesAbility to complete statistical programming… more
- Merck & Co. (Rahway, NJ)
- …and marketed productsReview and provide final approval of local registration study protocols when needed to obtain marketing authorization in secondary ... simultaneouslyReview and provide final approval Worldwide Marketing Applications, Clinical Study Reports, protocols, Investigator Brochures before release from our… more
- Merck & Co. (South San Francisco, CA)
- …of drug discovery and development. The senior specialist should demonstrate collaborative work spirit and excellent communication skills. - Within QP2, you have a ... as well as with external vendors and partners, on activities related to study design, protocol development, study execution, reporting and interpretation of… more
- Merck & Co. (Rahway, NJ)
- …- Facilitate manufacturing, packaging , and release of clinical supplies for clinical studies , assist in scale up activities at pilot and commercial scale, and ... independently design and execute complex experiments and data analysis. - Ability to work effectively with team members of diverse skill sets and backgrounds. -… more
- Merck & Co. (Rahway, NJ)
- …plans for all clinical supply activities associated with the clinical studies in their assigned compound(s)/ program(s). The incumbent must have demonstrated ... and ensures proper allocation of drug product as needed across studies within assigned program(s).-Responsible for identifying significant supply risks associated… 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 ... technological tools in the planning and managing of clinical supplies for assigned studies such as IRT & Microsoft PowerApps.--Works directly in the SAP system to… more
