- Daiichi Sankyo, Inc. (Bernards, NJ)
- …authoring, and management of Dose Preparation Instructions in support of clinical studies being conducted globally by Daiichi Sankyo. The candidate will ... collaborate globally with Formulation and Analytical Scientists, Clinical Operations, Regulatory Affairs CMC, and Clinical Development to collate the necessary… more
- Daiichi Sankyo, Inc. (Bernards, NJ)
- …trial (small size, standard complexity in design and geographic scope). Prepares clinical section of regulatory document. Collaborates as team member with AROs/CROs. ... documents under guidance of higher level. Reviews and oversee completion of clinical trial protocols. Provides medical and/or scientific direction to Clinical … more
- Katalyst HealthCares and Life Sciences (Matthews, NC)
- …appropriate. Coordinate data management timelines for individual projects and well as clinical programs, including database lock, DSMB meetings, data review ... Responsibilities: Leads, performs, and oversees data management activities for clinical studies and/or clinical programs. Performs hands-on clinical data… more
- Daiichi Sankyo, Inc. (Bernards, NJ)
- …study level. Publish shiny apps for study or against integrated database - Representing cross-functional collaborations on R capabilities and systems: Collaborate ... and across compounds safety reviews (ie, ILD). Collaborate with Clinical Development and Clinical Sciences for effective...methods using SAS or R required- Advanced knowledge in database structures and set-up required Travel: Ability to travel… more
- Washington University (St. Louis, MO)
- … Clinical Research Methods, Clinical Research Operations, Clinical Techniques, Critical Thinking, Database Management, Effective Written Communication, ... Scheduled Hours 40 Position Summary This position is in the Pediatric Clinical Research Unit (PCRU), an outpatient research unit located at St. Louis Children's… more
- Merck & Co. (North Wales, PA)
- …management; a general understanding of worldwide regulatory requirements; and with good clinical trial experience in Phase II/ III trials.- The knowledge must be ... principles and statistical methods applied to designing and analyzing clinical trials in support of worldwide regulatory submissions.This position involves… more
- Merck & Co. (Rahway, NJ)
- …projects under supervision in Late Development Statistics. --Interacts with Clinical , Regulatory, Statistical Programming, Data Management and other company Research ... Laboratories Scientists in designing and analyzing clinical trials, and in coordinating the statistical activities for clinical drug/vaccine projects.The… more
- The Ohio State University (Dublin, OH)
- … research capacity conducting clinical research studies required; prior clinical research database management desired; computer literacy with basic ... your candidate profile as it will transfer to your application. Job Title: Clinical Research Coordinator - Hematology Tissue Bank Department: CCC | Leukemia Tissue… more
- Genmab (NJ)
- …us!The Role:The Senior Statistical Manager acts as a biostatistician supporting the clinical development of compounds as compound lead, primarily up until proof of ... the vendorSupports compound responsible programmer in developing an integrated database specificationCDT member:Responsible for giving statistical input to overall… more
- Daiichi Sankyo, Inc. (Bernards, NJ)
- …and cultures.. Additionally, this position possesses advanced knowledge of clinical operations and relevant regulatory requirements. This position has advanced ... and risk managementResponsibilities: Leadership, Direction, and Strategy:In collaboration with Clinical Development and Clinical Operations as well as… more
- Genmab (NJ)
- …us!The RoleThe Associate Director acts as a statistical expert supporting the clinical development of compounds as compound and/or indication lead for both early ... responsibilities as described below. The Associate Director contributes to clinical development strategies and plans.Responsibilities:Compound/Indication LevelAct as lead and… more
- Merck & Co. (Rahway, NJ)
- …programming activities for multiple and/or late stage drug/vaccine clinical development projects. -Accountability predominantly includes the development and ... tables, listings, figures), the span of which range from individual clinical trials to world-wide regulatory application submissions and post marketing support.The… more
- Genmab (NJ)
- …Manager will support the Data Management, Statistics, Drug Safety, Medical, Clinical Pharmacology and Biomarker functions with the above by developing and ... consistencySupports the establishment and maintenance of Genmab SDTM and ADaM database standards.Performs database standards consistency checks on databases… more
- Merck & Co. (North Wales, PA)
- …: This position supports statistical programming activities for late stage drug/vaccine clinical development projects. This may include leadership of one or more ... tables, listings, figures), the span of which range from individual clinical trials to world-wide regulatory application submissions and post marketing support.… more
- Merck & Co. (North Wales, PA)
- …and gain input on research design and implementation of retrospective database studies, assessment of patient reported outcomes, epidemiological studies and economic ... access and identifies value evidence needs to provide strategic input into clinical and market development programs.- Brings strong payer and HTA/reimbursement focus… more
- Merck & Co. (San Diego, CA)
- …in developing and deploying robust bioinformatics pipelines.Familiarity with database management and data warehousing concepts, particularly for integrating ... diverse biological and clinical datasets.Familiarity with drug-target interaction databases and resources relevant to pharmaceutical research.Experience with … more
- Global Technical Talent (Oakland, CA)
- …of diagnostic information services empowering healthier lives. Leveraging the world's largest clinical lab database , we offer insights to identify and treat ... and professional environment. Performs with confidence, both the forensic and clinical specimen collection and processing duties following established practices and… 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 ... drug design, high-throughput experimentation.Experience with IT infrastructure such as database systems, cloud computing (such as Databricks, AWS), and… more
- Daiichi Sankyo, Inc. (Bernards, NJ)
- …work with Global Regulatory Affairs and cross-functional teams (eg, Quality, CSPV, Clinical Operations, Clinical Development, RA CMC) to keep processes, ... analyses for any issues identified, to define CAPAs/deviationsMaintain a GRA database for tracking process deviations / CAPAsCoordinate activities required to… more
- HonorVet Technologies (New Haven, CT)
- …Demonstrates positive attitude to the participant population to ensure trust in clinical research Performs database cleanup activities and other recruitment and ... Volunteer Recruitment Support is responsible for registering new and current clinical research participants and conducting a series of pre-screening procedures to… more
