- 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)
- …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. (Upper Gwynedd, 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. (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. (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)
- …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. (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)
- …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. (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
- 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
- Novo Nordisk Inc. (Boston, MA)
- …accounts and community advocacy partners. The Ecosystem Portfolio Specialist must work collaboratively with all stakeholders who influence business in the local ... to the Ecosystem Business Manager. The Ecosystem Portfolio Specialist also must work collaboratively work with all internal stakeholders. Essential Functions… more
- Merck & Co. (South San Francisco, CA)
- …dose-response and exposure-response analyses, disease modeling, trial simulation, optimal study designs, strategic decision analyses, economic modeling) with ability ... status, disability status, or other applicable legally protected characteristics.--As a federal contractor, we comply with all affirmative action requirements for… more
- Merck & Co. (Rahway, NJ)
- …for US regional symposia and educational meetingsReviews investigator-initiated study proposals prior to headquarters submissionManages regional programs (patient ... status, disability status, or other applicable legally protected characteristics.--As a federal contractor, we comply with all affirmative action requirements for… more
- Merck & Co. (Rahway, NJ)
- …line-of-sight for licensure and commercialization.-Responsible for planning and executing work to support commercialization of working cell banks, identification and ... results are reported clearly and accurately and effectively communicate study results to stakeholders via presentations and technical reports.-Collaborate with… more
- Merck & Co. (San Francisco, CA)
- …subject matter expert, the Associate Director within the QP2-IO Group will work closely with teams of highly collaborative, cross-functional scientists to contribute ... in Oncology, authoring regulatory documents (investigational new drugs/INDs, clinical study reports (CSRs), clinical trial applications (CTDs)), and representing… more
- Merck & Co. (Boston, MA)
- …As a subject matter expert, the Director within the QP2-IO Group will work closely with teams of highly collaborative, cross-functional scientists to contribute to ... in Oncology, authoring regulatory documents (investigational new drugs/INDs, clinical study reports (CSRs), clinical trial applications (CTDs), and representing… more
- Merck & Co. (Rahway, NJ)
- …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
- Novo Nordisk Inc. (Durham, NC)
- …- effective day one Guaranteed 8% 401K contribution plus individual company match option Family Focused Benefits including 14 weeks paid parental & 6 weeks paid ... family medical leave Free access to Novo Nordisk-marketed pharmaceutical...and that interim reviews are held so that their work is focused on those priorities, and they understand… more
