- Daiichi Sankyo, Inc. (Basking Ridge, NJ)
- …an equal opportunity employer including veterans and people with disabilities. Summary The Associate Director, Clinical Data Standards, is responsible for ... - Leadership, Direction, and Strategy:Leads implementation of Therapeutic level clinical data collection requirements including cross-functional standards… more
- Merck & Co. (North Wales, PA)
- …database set up)Lead medical monitoring team in review and interpretation of clinical data /medical protocol-deviations in collaboration with the Clinical ... position drives scientific planning, strategy and execution of Phase 1-4 clinical studies.-Under the direction of the Program Lead, you will collaborate… more
- Daiichi Sankyo, Inc. (Basking Ridge, NJ)
- …centered around rare diseases and immune disorders.SummaryThis position serves as the Clinical Safety Scientist Lead for a large, late-stage program or multiple ... surveillance and risk management in partnership with Product Safety Lead(s), Clinical Safety Physician(s), and cross-functional team in support of benefit risk… more
- Novo Nordisk Inc. (WA)
- …a difference? The Position Drives the understanding and delivery of quality clinical research (patient safety, rights and wellbeing; data reliability; scientific ... relevant regulatory requirements Ensure accuracy, validity and completeness of data collected at clinical trial sites in...validity and completeness of data collected at clinical trial sites in accordance with the protocol, Monitoring… more
- Merck & Co. (Rahway, NJ)
- …clinical studies using deep scientific knowledge, statistical analysis and high-quality data to support decision making in clinical trials.- Responsibilities ... and programming requests in close collaboration with stakeholders (statisticians/modelers) and clinical colleagues, retrieve the required data , transform the … more
- Merck & Co. (Rahway, NJ)
- …Quantitative Pharmacology and Pharmacometrics - Immune/Oncology (QP2-IO) team in the role of Associate Director QP2-IO team is part of the Global Clinical ... organization and has oversight over drug development aspects related to clinical pharmacology and pharmacometrics of oncology drugs from post-PCC to registration.… more
- Merck & Co. (North Wales, PA)
- …team members when opportunities arise. Primary Activities :Programmatically synthesize preclinical / clinical data into analysis ready structures from varied ... Specific Required Skills and Experience: Significant expertise in SAS and clinical trial programming including data steps, procedures, SAS/MACRO,… more
- Aequor (Thousand Oaks, CA)
- …Receipt (POR) Temperature Data Review and Assessment: - Review the temperature data from shipments to clinical sites - Assess temperature excursion events ... more of a preference. We can train candidates on our QMTS roles. Associate Supply Chain Description: Candidates will, under limited supervision and in compliance… more
- Merck & Co. (Rahway, NJ)
- …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
- Catalent (Emeryville, CA)
- Research Associate II, BioconjugationPosition Summary:Catalent Pharma Solutions in Emeryville, CA is seeking a Research Associate II who will be responsible for ... liquid chromatography) analysis of site-specific antibody-drug conjugates (ADCs). The Research Associate II reports to the Group Leader, Bioconjugation. This is a… more
- Merck & Co. (North Wales, PA)
- …be programmed, an understanding of statistical terminology and concepts.Familiarity with clinical data management conceptsExperience in CDISC and ADaM ... Specific Required Skills and Experience: Significant expertise in SAS and clinical trial programming including data steps, procedures, SAS/MACRO, SAS/GRAPH;… more
- Novo Nordisk Inc. (Plainsboro, NJ)
- …goals. Gather input from clinical and regulatory teams to understand clinical data / patient outcomes, identify market opportunities, address regulatory ... strategy, focusing on every touchpoint that impacts our customers. We leverage data and insights to inform our decision-making processes, ensuring that our… more
- Catalent (St. Petersburg, FL)
- Associate Scientist II, QCPosition SummarySt. Petersburg is our primary soft gel development and manufacturing facility in North America with capacity of 18 billion ... and to the safety of every patient, consumer and Catalent employee. The Associate Scientist II, Quality Control will Independently test, develop and implement assays… more
- Catalent (Harman, WV)
- Associate Director, Continuous ImprovementSummary:The Associate Director, Continuous Improvement will work collaboratively with the Sr Director of CI and the ... to the implementation of effective sustainable solutionsPromote the use of data and metrics for identifying improvement opportunities and problem solving… more
- Merck & Co. (Rahway, NJ)
- Job DescriptionBiologics Process R&D Associate ScientistOur Research Scientists are our Inventors.- Using innovative thinking, state-of-the-art facilities, and ... To achieve this, we work closely with colleagues in Discovery, Pre- clinical , Early Development, Analytical, Formulation, and Commercial Manufacturing while providing… more
- Merck & Co. (North Wales, PA)
- Job DescriptionWe are currently recruiting for the position of Associate Director, US Oncology - Hematology Scientific Strategy. This talented individual will lead ... a robust scientific leader (SL) engagement plan, coordinating with medical affairs, clinical research, and global marketing to provide a consistent One our Company's… more
- Novo Nordisk Inc. (Plainsboro, NJ)
- …policies and procedures. Relationships This position reports to a Senior Director within the Clinical Data Science & Evidence (CDSE) - RWE team. This role will ... About the Department The Clinical , Medical and Regulatory (CMR) department at Novo...with the FDA to providing medical education and collecting data to support efficacy and new product development, CMR… more
- Merck & Co. (Rahway, NJ)
- …enables gain of critical internal experience during scale-up of clinical supplies manufacturing, demonstration of new manufacturing technology/processes, training ... members to ensure the quality and safe delivery of clinical supplies, the scientific rigor of the processes, and...IH sampling activities for new or existing equipment. Support data rich experimentation at pilot scale via process analytical… more
- Merck & Co. (North Wales, PA)
- …of the role Preferred Experience and Skills: Ability to translate science/ clinical data into clear marketing strategies, medical education and/or ... including experience including bringing materials through legal, regulatory, and clinical review Strong project management skills as demonstrated by prioritizing… more
- Daiichi Sankyo, Inc. (Basking Ridge, NJ)
- …standards, and coding library management.Manages, reviews and approves medical coding of clinical data ensuring high quality; creates and manages the ... immune disorders. Summary Position manages the end-to-end delivery of medical coding data for assigned projects/studies collaborating with clinical and medical… more
