- Merck & Co. (Rahway, NJ)
- …be programmed, an understanding of statistical terminology and concepts.Familiarity with clinical data management conceptsExperience in CDISC and ADaM ... Primary Activities :Effective analysis and report programming development and validation utilizing global and TA standards and following departmental SOPs and… more
- Merck & Co. (St. Louis, MO)
- …reports to the Regional RMSD Team Leader - within US Medical Affairs, Global Clinical Development, Research and Development (R&D).--Location details: -This role ... (HH) strategies -Communicate external stakeholder opinions, insights and feedback on new data , clinical trends and the evolving vaccine landscape to Medical… more
- Merck & Co. (North Wales, PA)
- …be programmed; an understanding of statistical terminology and conceptsFamiliarity with clinical data management conceptsExperience in CDISC and ADaM ... Primary Activities: Effective analysis and report programming development and validation utilizing global and TA standards and following departmental SOPs and… more
- Daiichi Sankyo, Inc. (Bernards, NJ)
- …minimum of 7 years relevant experience required- Experience Qualifications- Experience in global clinical operations methods and processes in industry setting is ... or outsourced studies with elements of insourcing. This includes global operational execution and delivery of clinical ...achieve study milestones and deliverables according to agreed quality standards and timelines and that quality of data… more
- Merck & Co. (North Wales, PA)
- …project level Position Specific Required Skills and Experience: Programming expertise with clinical endpoint data (efficacy and safety) and pharmacokinetic ... in CDISC SDTM and ADaM standardsSignificant expertise in SAS and clinical trial programming including data steps, procedures, SAS/MACRO, SAS/GRAPHDesigns… more
- Genmab (NJ)
- …to inform study design and operational delivery strategies.Shape feasibility approaches and standards by incorporating internal and external data sources, novel ... feasibility within pharmaceutical, biotech, or CRO settings.Proven leadership of complex, global feasibility initiatives and ability to influence clinical … more
- Formation Bio (New York, NY)
- …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 ... processes, and capabilities to accelerate all aspects of drug development and clinical trials. Formation Bio partners, acquires, or in-licenses drugs from pharma… more
- Legend Biotech USA, Inc. (Raritan, NJ)
- …and system standards to ensure compliance with applicable Legend standards , industry standards , and global regulations.Interacts with colleagues ... Legend Biotech is a global biotechnology company dedicated to treating, and one...within a cell therapy manufacturing plant to support both clinical and commercial requirements in a sterile GMP environment.… more
- Aequor (Thousand Oaks, CA)
- …influence the reproducibility and reliability of critical reagents that support assays for clinical and commercial product testing across 's global network of ... Note: Fully Onsite The Thousand Oaks Global Critical Reagents (GCR) Team is looking for...engagement requires conformance with site policies, safety, quality, and data -integrity requirements. The successful candidate must model 's mission… more
- Daiichi Sankyo, Inc. (Bernards, NJ)
- …function as a member of the various cross-functional forums including, Publications Planning, Clinical and Safety sub-teams, US and Global Brand Team, and US ... to the creation and supply of innovative pharmaceutical therapies to improve standards of care and address diversified, unmet medical needs of people globally… more
