- Merck & Co. (North Wales, PA)
- … Principal Scientist) has primary responsibility for the planning and directing clinical research activities involving new or marketed Neuroscience Medicines. ... business about twenty (20) percent of the time to manage future or ongoing clinical research projects. Education MD or MD/Ph.D. Required Qualifications Must have… more
- Merck & Co. (North Wales, PA)
- …execution, monitoring, analysis, regulatory filing, and publication.Specifically, The Senior Director May Be Responsible For:Evaluating pre- clinical and ... Scientist) has primary responsibility for the strategic planning and directing clinical research activities involving investigational compounds in Immunology.… more
- Merck & Co. (Upper Gwynedd, PA)
- …--The Senior Director will report to an Associate Vice President in the Oncology Clinical Research Group. Under the guidance of a supervisor, the Senior ... Director has primary responsibility for the planning and directing of clinical research activities involving new or marketed Oncology medicines. Our Oncology… more
- Merck & Co. (Upper Gwynedd, PA)
- …Translational Medicine Operations, Translational Medicine-EU, Drug Metabolism/Modeling & Simulation, Regulatory Affairs, and late-stage Clinical Research ... clinical study support staff and scientists (including discovery research , biostatistics, drug metabolism, modeling and simulation, regulatory affairs,… more
- Merck & Co. (Upper Gwynedd, PA)
- …organization, which includes Global Medical and Scientific Affairs as well as Outcomes Research .Under the guidance of a senior leader, this position supports ... and barriers to reimbursement and market access, and provides input into clinical , regulatory , payer/access, marketing and evidence generation strategies and… more
- Merck & Co. (North Wales, PA)
- …of an Executive Director, within the Value and Implementation, Outcomes Research the incumbent has the following responsibilities:1) development of the integrated ... and/or vaccines on a worldwide basis and3) development and implementation of Outcomes Research (OR) and Real World evidence programs to meet the value evidence needs… more
- Merck & Co. (North Wales, PA)
- …and quality management of submission data standard deliverables for world-wide regulatory application submissions of drug and vaccine clinical development ... keeping current with industry submission data standards including SDTM, ADaM, clinical site data for CDER inspection planning, etc.Responsible for continuous… more
- Olympus Corporation of the Americas (Center Valley, PA)
- … clinical trials. This role ensures the integrity, accuracy, and completeness of clinical trial data in compliance with regulatory standards, SOPs, and Good ... Duties** + Work collaboratively with other Data Managers, Programmers, Biostatisticians, Clinical Operations, Medical Directors, and Regulatory staff to meet… more
- Olympus Corporation of the Americas (Center Valley, PA)
- …data, including facilitating the resolution of data queries under the guidance of the Clinical Research Associate (CRA), Data Management and/or the Clinical ... and collection of study-specific documents required in the site's Regulatory Binder. + Assist in tracking study activies and...Minimum of two (2) or more years experience in clinical research , with medical device and/or pharmaceutical… more
- Legend Biotech USA, Inc. (Philadelphia, PA)
- …strategy from early research through IND-enabling studies and into clinical development, ensuring regulatory compliance and scientific rigor in support ... scientific and strategic input to project teams across discovery, preclinical, regulatory , and clinical functions.Manage non-GLP and GLP-compliant studies… more
