- 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. (Rahway, NJ)
- …and programsIn collaboration with internal teams and external partners, designs studies , authors study protocols, develops measurement questionnaires, case ... Job DescriptionRole SummaryUnder the guidance of a senior leader, an Associate Principal Scientist/ Associate Director, has primary responsibility for… more
- Merck & Co. (Boston, MA)
- …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. (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 cr o...with external vendors and partners, on activities related to study design, protocol development, study execution, reporting… more
- Twist BioScience (South San Francisco, CA)
- Research Associate II (Onsite in South San Francisco) Job DescriptionThe R&D team at Twist is searching for a curious, thoughtful, and driven individual with ... our silicon-based, massively-parallel DNA synthesis platform, you will conduct laboratory studies to develop, improve, and troubleshoot our latest NGS products. In… 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. (North Wales, PA)
- ….Supervises development of clinical documents including protocols, clinical study reports and background documents.Interfaces with functional experts across ... Job DescriptionThe Associate Vice President (AVP)/Section Head, Global Clinical Development, Pediatrics will focus on driving strategy, development, and life-cycle… 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
- 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 in the ... technical skills in SAS systems and application development and experience. The Associate Director must be a highly specialized individual contributor or functional… more
- Merck & Co. (Rahway, NJ)
- …who are passionate about driving impactful changes. Position Overview: As the Associate Director of Launch Strategy and Operations, you will lead the enterprise ... Making, Developing Proposals, Employee Performance Evaluations, Environmental Scanning, Feasibility Studies , Go-to-Market Strategies, Immunochemistry, Immunotherapy, Life Science, Management Process,… 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
- 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 improved… 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
- 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
- Eisai, Inc (Nutley, NJ)
- …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 the ... and to ensure compliance with Eisai policies & standard operating procedures.Self- study to ensure scientific credibility of existing and new therapeutic areas… more
- Aequor (Walkersville, MD)
- …High School Diploma or Equivalent minimum; AS/BS preferred Preferred area of study : Science related discipline 0-3 years' experience; some prior experience in a ... manufacturing setting preferred. Proven logic and decision-making abilities, critical thinking skills Hours: 7:30AM - 4:00PM Visual Acuity Test (eye exam) Required - pre-start 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
- 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 and ... as supporting technology transfer to external partners (as required). The Associate Director sets strategic directions and project priorities, providing scientific… more
- Aequor (North Creek, WA)
- …(Required): Position Summary: We are seeking an experienced, highly motivated Research Associate to join our Manufacturing Science and Technology (MSAT) lab team in ... equipment setup, culture maintenance, and cleanup Designing and executing experimental studies with increasing complexity (OFAT and DOE) Independent data analysis… more
- Genmab (NJ)
- …like a fit? Then we would love to have you join us!The RoleThe Associate Director acts as a statistical expert supporting the clinical development of compounds as ... trial responsible statistician with responsibilities as described below. The Associate Director contributes to clinical development strategies and plans.Responsibilities:Compound/Indication… more
