- Genmab (NJ)
- …and feel like a fit? Then we would love to have you join us!Role:The Associate Director acts as a statistical expert supporting the clinical development of ... as trial responsible statistician with responsibilities as described below. The Associate Director contributes to clinical development strategies and… more
- Merck & Co. (South San Francisco, CA)
- …West Point, PA / Rahway, NJ is seeking a curious and collaborative Associate Director to support our rapidly expanding cardiometabolic and ophthalmology ... pipelines. - As an Associate Director , you will represent QP2 on...with external vendors and partners, on activities related to study design, protocol development, study execution, reporting… 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 ... expanding late-stage biologics portfolio.Drive Innovation: Conduct laboratory-scale and manufacturing-scale studies to support commercial process validation and characterization. You'll… 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 ... Job DescriptionAssociate Director , Launch Strategy and OperationsLocation: North Wales (Upper Gwynedd), PennsylvaniaDivision: Human Health US (HH-US)Therapeutic… more
- Merck & Co. (Rahway, NJ)
- Job DescriptionRole SummaryUnder the guidance of a senior leader, an Associate Principal Scientist/ Associate Director , has primary responsibility for ... and programsIn collaboration with internal teams and external partners, designs studies , authors study protocols, develops measurement questionnaires, case… more
- Merck & Co. (San Francisco, CA)
- Job Description Position Description: Associate Director , DSCS Digital Implementation Project ManagerWithin the Development Sciences and Clinical Supply (DSCS) ... Under the broad guidance of the DSCS Digital Program Mgmt Lead, the Associate Director , DSCS Digital Project Manager, will be responsible for implementing… more
- Eisai, Inc (Exton, PA)
- …difference. If this is your profile, we want to hear from you. The Associate Director of Biologics Operations Upstream and Downstream is responsible for leading ... well as supporting technology transfer to external partners (as required). The Associate Director sets strategic directions and project priorities, providing… more
- Eisai, Inc (Nutley, NJ)
- …If this is your profile, we want to hear from you. The Associate Director , Clinical Programming must have expertise in addressing technical challenges ... technical skills in SAS systems and application development and experience. The Associate Director must be a highly specialized individual contributor or… more
- Eisai, Inc (Nutley, NJ)
- …a difference. If this is your profile, we want to hear from you. The Associate Director (AD), Global Medical Affairs Training and Education is responsible for ... & International). Eisai Salary Transparency Language:The base salary range for the Associate Director , Global Medical Affairs Training and Education is from… more
- Merck & Co. (North Wales, PA)
- …support for Oncology programs.- The position reports to the Senior Director responsible for Portfolio Real-world Evidence (RWE) in Oncology.- -Position objectivesTo ... design and execute real-world evidence studies , designed to demonstrate the value of new products in support of HTA, reimbursement, provider, payer and patient… more
- Merck & Co. (North Wales, PA)
- …Clinical Trial Team lead. Leads and directs teams in key study planning, development, and execution elements (eg operational reviews, issue escalation/mitigations, ... Responsible for facilitating and collaborating with key internal/external stakeholders ( study team, subsidiary country teams, vendors, committees, etc.) in support… more
- Merck & Co. (Upper Gwynedd, PA)
- Job DescriptionGRACS CMC - Associate Principal Scientist, CMC, R4 - Pharm Pre-approval Reporting to the Sr Director / Director /Principal Scientist/Sr Principal ... or a related field (advanced degree preferred). Fields of study include Pharmacy, Chemical Engineering, Biology, Microbiology, or BiochemistryRequired Experience… more
- Daiichi Sankyo, Inc. (Bernards, NJ)
- …and statistical aspects for safety signal detection and characterization for ongoing studies and compound level pooled clinical trial data of project(s). Act as ... statistical expert consultant within company for safety analyses.Responsibilities:- Lead for safety signal statistical handling, lead the statistical support in safety signal detection, validation, characterization and reporting in collaboration with safety… more
- Merck & Co. (Rahway, NJ)
- …management and ensures proper allocation of drug product as needed across studies within assigned program(s) . - Responsible for identifying significant supply risks ... associated with clinical bulk activities in addition to serving in a lead role for clinical supply issue escalation within their program(s) (and subsequent manage thereof) to GCS Leadership . - - Responsible for the clinical supply budget for respective… more
- Daiichi Sankyo, Inc. (Bernards, NJ)
- …CSPV and with CROs, vendors, and partners; and participates on interdepartmental study teams. This level handles escalated global CSPV case processing issue and ... oversight groups for case processing activities and reports to the Director of PV Case Management.Responsibilities:ICSR Processing: Oversees QC activities, supports… more
- Daiichi Sankyo, Inc. (Bernards, NJ)
- …programming innovation outside of DS and establish the company reputations and images.- Develop study specific shiny apps or execute shiny apps at study level. ... Publish shiny apps for study or against integrated database- Representing cross-functional collaborations on R capabilities and systems: Collaborate with RD non-BDM and non-RD R user group or developers. Collaborate with biostat innovation to enhance BDM… more
- Merck & Co. (Rahway, NJ)
- …for complex workstreams and implement capital project scope and technical studies that support business objectives, with focus on Process Design and ... Process Safety for Small Molecule High Potency/Containment Projects. Develop project scope, front-end planning, and provide innovative designs and solutions that meet business objectives. Provide technical guidance during projects, assess viability of… more
- Daiichi Sankyo, Inc. (Bernards, NJ)
- …testing, for less complex projects.At the time of implementation of a CDx study /IVDR performance evaluation study integration of an assay into clinical testing ... (before testing) and once data is ready for CDx submission (after testing)Serve as the Point of Contact (PoC) for gathering country/region specific CDx RA requirements from local RA team members (eg from Japan, China, Australia, Canada, Korea etc.)For… more
- Daiichi Sankyo, Inc. (Bernards, NJ)
- …to Clinical Operations. Represents Clinical Development on Project Teams.Responsibilities: Study Strategy: Provides the strategic direction to Biostatistics Data ... Reviews patient population and protocol compliance for consistency with study strategy; Develops biomarker strategy in collaboration with Translational Medicine/Clin… more
- Proskauer (New York, NY)
- …sports leagues, entertainment industry legends and other industry-redefining companies. The Associate Director of Practice Management - Corporate (" Associate ... training, developing and retaining highly accomplished and dedicated attorneys. Specifically, the Associate Director will work with practice group heads to… more
