- Daiichi Sankyo, Inc. (Basking Ridge, NJ)
- …to ensure appropriate biomarker, PK / PD measurements, Reviews emerging clinical data regularly, Leads dose-escalation meetings, Performs quality assessment ... program in a specific indication, ie, multiple multinational phase II/III clinical trials; Reviews regulatory documents from cross functional, holistic perspective;… more
- Merck & Co. (North Wales, PA)
- … trial team.Leading medical monitoring team in review and interpretation of clinical data /medical protocol deviations in collaborations with the Clinical ... in collaboration with Data Management/Programming.Collaborating cross-functionally to monitor clinical data to ensure quality, completeness, and integrity of… more
- Merck & Co. (Rahway, NJ)
- Job DescriptionPosition Description: Manager, Operations and Reference Data Management, Global Clinical Data Standards Working closely with the Global ... Clinical Data Standards (GCDS)...insights into implementation of strategic direction.In support of the Senior Director, Operations and Reference Data Management,… more
- Merck & Co. (Rahway, NJ)
- …existing and pipeline products to produce safe, effective, innovative medicine.The Global Clinical Data Standards Vocabulary Specialist, Associate Director, is a ... for growth opportunitiesThe Vocabulary Specialist may lead or participate in:Internal clinical data standards forumsStandards development teams and data… more
- George Washington University (Washington, DC)
- …poisonings, save lives, and limit injury from poisoning.The NCPC is seeking a Senior Poison Center Administrator, Clinical Operations. The incumbent trains and ... produce at least 1 QA project, annually. Run monthly data clean-up in Toxicall and correct charts as needed...or CSPI certification (until ABAT certified). Maintain expertise in clinical toxicology and knowledge of current operations of US… more
- Merck & Co. (North Wales, PA)
- …submissions) per regulatory requirements and industry guidelines.Ability to present clinical data clearly and objectively, with minimal supervision.Demonstrated ... clinical regulatory writing portfolio. With minimal oversight, the Senior Medical Writer:Demonstrates independence in preparing clinical regulatory documents… more
- Russell Tobin & Associates (Minneapolis, MN)
- …with healthcare administrative data , including claims and enrollment. Familiarity with clinical data domains and code sets (eg, CPT, ICD, DRG). Russell ... What are we looking for in our Senior Provider Data Anlyst? Location: Remote/Telecommute Duration : 6+months Pay : $25 - $33/ hr on w2 Join our dynamic team of 7… more
- Eisai, Inc (Nutley, NJ)
- …monitors study conduct to proactively address issues to ensure high quality study data (as needed). Clinical Study Report - provides statistical and validation ... we want to hear from you. Job Summary The Senior Manager, Translational Science Biostatistics will be expected to...efforts of Translational Science to generate useful human biomarker data sets from internal (eg clinical samples,… more
- Daiichi Sankyo, Inc. (Basking Ridge, NJ)
- …TMCP to ensure appropriate biomarker, PK / PD measurements, Reviews emerging clinical data regularly, Leads dose-escalation meetings, Performs quality assessment ... program in a specific indication, ie, multiple multinational phase II/III clinical trials; Reviews regulatory documents from cross functional, holistic perspective;… more
- Daiichi Sankyo, Inc. (Basking Ridge, NJ)
- …to ensure appropriate biomarker, PK / PD measurements; Reviews emerging clinical data regularly; Leads dose-escalation meetings; Performs quality assessment ... trial (small size, standard complexity in design and geographic scope). Prepares clinical section of regulatory document. Collaborates as team member with AROs/CROs.… more
- Daiichi Sankyo, Inc. (Basking Ridge, NJ)
- …research areas centered around rare diseases and immune disorders.Summary The Senior Director, Global Oncology Medical Affairs is responsible for developing the ... as a member of the various cross-functional forums including, Publications Planning, Clinical and Safety sub-teams, Global Brand Team, and Global Product Team to… more
- Merck & Co. (Rahway, NJ)
- …related drug/vaccine projects in Late Development Statistics.Lead the interaction with Clinical , Regulatory, Statistical Programming, Data Management, and other ... and ascertains needs for potential program development of novel statistical methodology.Analyzes data and interprets results from clinical trials to meet… more
- Merck & Co. (Rahway, NJ)
- Job DescriptionWe are seeking applications for a Senior Scientist position available at the Rahway, NJ research facility. Join Small Molecule Analytical Research and ... and dedicated colleagues while developing and expanding your career.In your role as Senior Scientist, you will be part of a team developing innovative analytical… more
- Novo Nordisk Inc. (Boulder, CO)
- …network performance for data capture and analysis locally and globally. The Senior IT Engineer I - Labs will therefore be working closely with research and ... the full R&D continuum, from early research through late-stage clinical development. Here, we are building for the future,...you ready to make a difference? The Position The Senior IT Engineer I - Labs will be responsible… more
- Merck & Co. (Rahway, NJ)
- …provides a high degree of technical and project management responsibility. The Senior Specialist - Manufacturing Automation position will report to the Director, ... production, utility systems and associated infrastructure.- Responsibilities of the Senior Specialist - Manufacturing Automation include the following:The automation… more
- Eisai, Inc (Nutley, NJ)
- …to develop and execute the medical affairs plan, including data generations (including RWE), post-marketing research, medical education, research grants, ... provides strategic development, planning, implementation, and oversight of Phase IV clinical trial programs within the Medical Affairs department. She/He utilizes… more
- Lundbeck (Miami, FL)
- …airport. Territory consists of Florida, Georgia and Puerto Rico SUMMARY: The Senior MSL, Neurology will apply advanced field based medical and scientific experience, ... inform medical strategies and contribute towards identifying unmet medical needs and data gaps Identifies and facilitates the submission of grant requests and… more
- Merck & Co. (Rahway, NJ)
- Job DescriptionJoin our team as a Clinical Quality Operations Lead - Inspection Strategy and be at the forefront of developing and implementing policies, processes, ... with other functions within and outside of GCTO to ensure that Good Clinical Practice Health Authority inspections are adequately supported and managed and that QCO… more
- Merck & Co. (Rahway, NJ)
- …and coordinating statistical activities supporting drug/vaccine projects.Interacts with Clinical , Regulatory, Statistical Programming, Data Management, and ... project management experiences are necessary.Solid knowledge of statistical analysis methodologies, clinical trial designs, and statistical and data processing… more
- Merck & Co. (North Wales, PA)
- Job DescriptionRole Summary:The Global Senior Director Medical Affairs (GDMA) Immunology/Pipeline & Biomarkers will be responsible for driving execution of ... and regionsServes as an impactful member of Product Development Team sub-teams ( Clinical , Value Evidence, Commercial, Publications and Label) and Global Human Health… more
Related Job Searches:
Clinical,
Clinical Data,
Clinical Senior,
Data,
Data Senior,
Senior,
Senior Clinical Data Analyst,
Senior Clinical Data Management,
Senior Lead Clinical Data,
Senior Manager Clinical Data