- Merck & Co. (Rahway, NJ)
- Job DescriptionThe Clinical Research Director (CRD) is the Clinical Operations lead in a country/cluster and is responsible-for execution of all ... country /-cluster to deliver clinical trials as per global clinical research pipeline requirement.Strategic country / cluster representative for initiatives… more
- Formation Bio (New York, NY)
- … will manage a team of Clinical Trial Managers (CTMs) and Clinical Research Associates (CRAs) and will collaborate closely with cross-functional teams to ... pharma companies, research organizations, and biotechs to develop programs past clinical proof of concept and beyond, ultimately helping to bring new medicines… more
- Merck & Co. (Rahway, NJ)
- …the guidance of a senior leader, a Senior Principal Scientist/Senior Director , has primary responsibility for developing value evidence strategies, and ... resource utilization and costs, physician and patient satisfaction surveys, clinical and patient reported outcomes assessments, systematic reviews and meta-analyses,… more
- Merck & Co. (Rahway, NJ)
- Job DescriptionUnder the guidance of a senior leader, a director has primary responsibility for developing value evidence strategies, and planning/managing real ... world and outcomes research activities for in-line and pipeline products to meet the value evidence needs of clinicians, health systems, payers, policymakers, and… more
- Merck & Co. (Rahway, NJ)
- …position resides within our company's Value and Implementation (V&I), Outcomes Research organization, which is responsible for real-world evidence generation and ... outcomes research to enable sustained patient access to our company's...in collaboration with internal teams, and provide input into clinical , payer/access, marketing and value evidence generation strategies and… more
- Merck & Co. (Rahway, NJ)
- …Clinical Supply (GCS) organization is accountable for managing the 'end-to-end' integrated clinical supply chain across the full our Research & Development ... GCS is accountable for the planning, sourcing, labeling, packaging and delivery of clinical supplies to clinical sites globally. The GCS Planning (Planning)… more
- Merck & Co. (Rahway, NJ)
- … Clinical Development, has primary responsibility for the planning and directing clinical research activities involving new or marketed drugs in the Oncology ... Clinical Research group and in the field...will interact externally with key opinion leaders.-Specifically, the Executive Director , PDT Lead may be responsible for:-Evaluating pre- clinical… more
- Merck & Co. (Rahway, NJ)
- …applicant would be expected to interact across all Pharmaceutical Sciences & Clinical Supply (PSCS) and our Research Division locations.Current Employees apply ... Job DescriptionThe Executive Director , Device Technical Operations is a pivotal leadership...the Device Development & Technology (DD&T) organization in our Research Division. This position is responsible for providing strategic… more
- Merck & Co. (Rahway, NJ)
- Job DescriptionIn this Principal Scientist/ Director position within Translational Oncology, this team member will provide leadership for aligned and integrated ... Teams (ADTs) and our diagnostic partners.-Position reports to Executive Director , CDx. Primary Responsibilities : Direct CDx/IVD development projects, including… more
- Formation Bio (New York, NY)
- …pharma companies, research organizations, and biotechs to develop programs past clinical proof of concept and beyond, ultimately helping to bring new medicines ... progress because of the high cost and time of clinical trials. Recognizing that this development bottleneck may ultimately...Bio is seeking a highly skilled and experienced Senior Director , Biostatistics to join our dynamic team. This critical… more
- Merck & Co. (Rahway, NJ)
- …clinical through clinical development and into commercial supply.The Executive Director reports to the Vice President, Analytical Research & Development ... Job DescriptionThe Executive Director for Cell Based Sciences within Analytical R&D...works closely with leaders and scientists within the Discovery, Pre- clinical Development, Manufacturing, Quality Assurance and Regulatory organizations and… more
- Formation Bio (New York, NY)
- …pharma companies, research organizations, and biotechs to develop programs past clinical proof of concept and beyond, ultimately helping to bring new medicines ... progress because of the high cost and time of clinical trials. Recognizing that this development bottleneck may ultimately...to patients faster and more efficiently.About the PositionThe Sr. Director , GMP Quality Assurance will lead the GMP QA… more
- Formation Bio (New York, NY)
- …pharma companies, research organizations, and biotechs to develop programs past clinical proof of concept and beyond, ultimately helping to bring new medicines ... than the industry can progress because of the high cost and time of clinical trials. Recognizing that this development bottleneck may ultimately limit the number of… more
- Formation Bio (New York, NY)
- …pharma companies, research organizations, and biotechs to develop programs past clinical proof of concept and beyond, ultimately helping to bring new medicines ... than the industry can progress because of the high cost and time of clinical trials. Recognizing that this development bottleneck may ultimately limit the number of… more
- Formation Bio (New York, NY)
- …pharma companies, research organizations, and biotechs to develop programs past clinical proof of concept and beyond, ultimately helping to bring new medicines ... than the industry can progress because of the high cost and time of clinical trials. Recognizing that this development bottleneck may ultimately limit the number of… more
- Formation Bio (New York, NY)
- …pharma companies, research organizations, and biotechs to develop programs past clinical proof of concept and beyond, ultimately helping to bring new medicines ... than the industry can progress because of the high cost and time of clinical trials. Recognizing that this development bottleneck may ultimately limit the number of… more
- Merck & Co. (Rahway, NJ)
- …, Trial and Site Management Product Line - - Job Description - - Our Company Research Labs IT team partners with the Clinical Trial Operations teams within the ... attendance is required for, field-based positions; facility-based, manufacturing-based, or research -based positions where the work to be performed is located… more
- Merck & Co. (Rahway, NJ)
- …role of Associate Director QP2-IO team is part of the Global Clinical Development organization and has oversight over drug development aspects related to ... clinical pharmacology and pharmacometrics of oncology drugs from post-PCC...communication skills. As a subject matter expert, the Associate Director within the QP2-IO Group will work closely with… more
- Merck & Co. (Rahway, NJ)
- Job DescriptionAssociate Director - Pharmacometrics, Quantitative Pharmacology and PharmacometricsThe Quantitative Pharmacology and Pharmacometrics (QP2) department ... at our company, this position offers an opportunity for the Associate Director to drive pipeline impact across therapy areas.This Associate Director … more
- Merck & Co. (Rahway, NJ)
- …decision-making at our company, this position offers an opportunity for the Director to drive pipeline impact and mentor/coach a talented group of ... pharmacometricians.The Director -Pharmacometrics will work with scientists within QP2 by proactively evaluating and incorporating one or more of the following… more
