- Merck & Co. (Rahway, NJ)
- …to customers both internal and external to GCS and serve s as the lead GCS spokesperson at clinical and development related meetings .- Working independently, ... lead GCS Planning program representative ) such as clinical development, regulatory, quality and other supply chain areas...working a Hybrid work consisting of three total days on- site per week, Monday - Thursday, although the specific… more
- Merck & Co. (North Wales, PA)
- Job DescriptionThe Associate Vice President (AVP)/Section Head, Global Clinical Development, Pediatrics will focus on driving strategy, development, and ... pediatric vaccines in the Therapeutic Area. The incumbent will be expected to lead multiple programs that are in various stages of development therefore requiring… more
- Merck & Co. (Rahway, NJ)
- Job DescriptionDevice Development Associate Principal Scientist - Development Strategy, Design Controls( Associate Director Equivalent) Our company's Device ... enabled combination products to achieve safe and effective delivery to their intended site of action.- The DD&T Team manages the development of the device… more
- Merck & Co. (North Wales, PA)
- …operational planning, feasibility, execution and conduct of clinical trial(s).Serves as the Clinical Trial Team lead . Leads and directs teams in key study ... the operational planning and execution of one or more clinical trials. In this position, you will have the...working a Hybrid work consisting of three total days on- site per week, Monday - Thursday, although the specific… more
- Merck & Co. (Durham, NC)
- …to align to SAP and business processes related to any new project implementations. Site supply chain lead and coordinator for the successful implementation of ... warehousing and logistics operations, both on the main campus as well as off- site (3rd party) storage facilities.- The successful candidate will be responsible for… more
- Merck & Co. (San Francisco, CA)
- …data-driven decision-making. Under the broad guidance of the DSCS Digital Program Mgmt Lead , the Associate Director, DSCS Digital Project Manager, will be ... Job Description Position Description: Associate Director, DSCS Digital Implementation Project ManagerWithin the Development Sciences and Clinical Supply (DSCS)… more
- Merck & Co. (Rahway, NJ)
- Job DescriptionJoin Our Team as an Associate Principal Scientist/ Associate Director in Biologics Drug Substance Commercialization!Are you ready to make a ... Downstream Purification-department is seeking a passionate and skilled individual to lead the charge in transforming our late-stage pipeline and commercial products… more
- Merck & Co. (Rahway, NJ)
- …individuals who are passionate about driving impactful changes. Position Overview: As the Associate Director of Launch Strategy and Operations, you will lead the ... leadership capabilities. Key Responsibilities include: Strategic LeadershipLaunch Strategy Development: Lead the creation of holistic, integrated launch plans that… more
- Merck & Co. (Rahway, NJ)
- …biologics, vaccine) Drug Product development and Good Manufacturing Practice (GMP) clinical supply manufacturing facility in Rahway, New Jersey.The Sterile Process ... Engineer role at the Associate Director level will leverage the individual's leadership, technical,...and communication skillsets to drive the success of our clinical manufacturing facility and organization. As the facility is… more
- Merck & Co. (San Francisco, CA)
- …of decision-making at our Company, this position offers an opportunity for the Associate Director to drive pipeline impact across therapy areas. - This Associate ... PK/PD models, exposure response (ER) models, model-based meta-analysis (MBMA), clinical trial simulations (CTS) and disease progression modeling into programs… more
- Merck & Co. (Rahway, NJ)
- Job DescriptionAs a Technical Lead , you will report into Director, Chemical Technical Operations, External Manufacturing API Technology, and play a pivotal role in ... groups during New Product Introductions/Technical Transfers and new technology.Offer on- site support at External Partners as required, proactively identifying risks… more
- Merck & Co. (Rahway, NJ)
- …that accelerate the decision-making process from hit identification to clinical candidate delivery across different therapeutic areas and modalities at ... statistics, and cheminformatics techniques to improve hit identification and hit-to- lead processes for different screening technologies (mRNA display, DNA-Encoded… more
- Genmab (NJ)
- …to have you join us!The Global Regulatory Labeling, Policy and Intelligence Associate Director will primarily be responsible for leading the development and ... patient information) for the Genmab portfolio of products. The lead may also be responsible for supporting various regulatory...position may be based in our Princeton, New Jersey site (which requires onsite presence 60% of the time… more
- Merck & Co. (Rahway, NJ)
- …Biopharmaceutics, the large molecule product development Director will influence the strategy, lead activities, and develop a team whose roles include design and ... opportunity is fast paced and contributes to the Pharmaceutical Sciences and Clinical Supplies (PSCS) deliverable which is the development of robust compositions,… more
- Merck & Co. (Rahway, NJ)
- …scientific & medical affairs plans for their assigned Therapy Areas (TA). They build and lead a team of TA dedicated global and regional directors and associate ... Global Brand and V&I Outcomes Research leads to define clinical development plans and brand strategies for assigned TAsProvides...working a Hybrid work consisting of three total days on- site per week, Monday - Thursday, although the specific… more
- Merck & Co. (North Wales, PA)
- …and vaccines for the benefit of patients and global human health.The Associate Vice President (AVP), Late Development Statistics, BARDS, is responsible and ... President in BARDS and will work collaboratively with other leaders in Clinical Development and Global Regulatory Affairs.--The AVP provides leadership and direction… more
- Merck & Co. (Rahway, NJ)
- …SM PR&D pipeline. Responsibilities: Under the scientific direction of a facility lead , the Operations Specialist will participate in equipment setups, raw material ... aiding technology development, and supplying Active Pharmaceutical Ingredient (API) for clinical use and drug product development. This will involve handling of… more
- BioSpace (New York, NY)
- …CRO liaison for all activities related to CRA performance, monitoring deliverables, and clinical site data quality. They will also assist with the implementation ... needs via oral or enteral routes. Job Overview: The Clinical Trial Manager (CTM)/ Clinical Research Associate...subject safety. They will play a critical role in clinical data review, management/escalation of site -level issues,… more
- Alira Health (Framingham, MA)
- …honest, be inclusive and elevate others. Job Description Summary Job Description ROLE The Clinical Research Associate is an important member of the Alira Health ... CRAs are highly motivated and function independently to conduct site monitoring responsibilities for clinical trials. CRAs... trials. CRAs work closely with the In-house CRAs, Lead CRAs, Director of Clinical Monitoring and… more
- University of Iowa Hospitals & Clinics (Iowa City, IA)
- …as either a Clinical Trials Research Assistant, requisition 25004144 or Clinical Trials Research Associate , requisition 25004146, based on the qualifications ... Description BASIC FUNCTION Support, conduct and manage the regulatory aspect of clinical trials to deliver and evaluate research protocols and clinical trials in… more
