- Merck & Co. (Boston, MA)
- …twenty (20) percent of the time to manage future or ongoing clinical research projects. Education Requirements:M.D., DO, MD/Ph.D, or DO/PhDRequired Experience and ... Job DescriptionThe Executive Clinical Director (Distinguished Scientist) has primary responsibility for the strategic planning and directing clinical research… more
- Daiichi Sankyo, Inc. (Bernards, NJ)
- …centers globally in partnership with other cross-functional leaders.- Contribute to Clinical Development initiatives, global education , and process development ... employer including veterans and people with disabilities. SummaryThis position will be the Clinical Science Group Lead in late phase development in the Global … more
- Merck & Co. (Rahway, NJ)
- …about twenty (20) percent of the time to manage future or ongoing clinical research projects. QualificationsMinimum education required: - MD or MD/Ph.D.Required ... Principal Scientist) has primary responsibility for the planning and directing clinical research activities involving new or marketed Oncology medicines. Our… more
- Novo Nordisk Inc. (Atlanta, GA)
- …trials in all stages of development. Incumbents have a deep scientific and clinical education and experience. Within Field Medical Affairs, this position ... Coordinates with key internal stakeholders to provide customized and dedicated system-wide clinical education and support within respective IHNs and coordinate… more
- Daiichi Sankyo, Inc. (Bernards, NJ)
- …and in the real-world setting.Contributes to creation and improvement of Clinical Development processes. Education :MD required; prefer Board certification in ... A cross-Oncology Development Medical Doctor position reporting to the Head Clinical Development Functional Excellence. This position complements CSPV and GMA efforts… more
- The University of Tennessee Health Science Center,… (Memphis, TN)
- …locations in Memphis, Knoxville, Chattanooga, and Nashville, as well as more than 100 clinical education sites across Tennessee. UTHSC is the largest educator of ... and the global community by fostering integrated, collaborative, and inclusive education , research, scientific discovery, clinical care, and public service.… more
- Merck & Co. (North Wales, PA)
- …location strategies. Contributes to the strategic vision and optimization of Global Clinical Trial Organization. Education Requirements: BA or BS degree, ... Data Management & Standards (GDMS) is responsible for ensuring that all clinical data management products and services are effectively delivered with high quality… more
- Merck & Co. (North Wales, PA)
- …Involved in research activities for innovative statistical methods and applications in clinical trial development. Minimum education required: PhD or equivalent ... projects under supervision in Late Development Statistics. --Interacts with Clinical , Regulatory, Statistical Programming, Data Management and other of our… more
- Daiichi Sankyo, Inc. (Nashville, TN)
- …research, academic or US-managed markets preferredPrevious experience in Oncology, clinical research and medical education preferred Principal MSL/Associate ... practice, research, academic or US managed markets preferredPrevious experience in Oncology, clinical research and medical education preferred Must have a valid… more
- Daiichi Sankyo, Inc. (Bernards, NJ)
- …rare diseases and immune disorders. Summary Provide support for all aspects of Global Clinical Operations with a high degree of quality in the execution of all ... and Medical Access/Expanded Access (MAP)/(EAP)activities in adherence to Good Clinical Practices (GCPs), appropriate Standard Operating Procedures (SOPs), Food and… more
- Daiichi Sankyo, Inc. (Bernards, NJ)
- …and geographic scope. Such trials could be pivotal for submission; Prepares clinical section of regulatory documents; Oversees management and performance of CRO; ... of key submission documents; Point of contact for interactions with regulatory-agency clinical reviewing divisions on clinical matters; Represents Clinical … more
- Daiichi Sankyo, Inc. (Bernards, NJ)
- …and geographic scope. Such trials could be pivotal for submission; Prepares clinical section of regulatory documents; Oversees management and performance of CRO; ... of key submission documents; Point of contact for interactions with regulatory-agency clinical reviewing divisions on clinical matters; Represents Clinical … 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
- Daiichi Sankyo, Inc. (Bernards, NJ)
- …disorders. Summary This position will be part of the Quantitative Clinical Pharmacology (QCP) team and support drug development and commercialization activities. ... It is accountable for the Clinical Pharmacology and Model-Based Drug Development (MBDD) plans and deliverables. The primary responsibilities of Clinical … more
- Daiichi Sankyo, Inc. (Bernards, NJ)
- …disabilities.SummaryThe Associate Director will be responsible for developing and implementing Clinical Pharmacology and Modeling & Simulation plans from FIH to post ... registration. Responsibilities include the development of Clinical Pharmacology and Modeling and Simulation plans, design and lead study teams to execute Clinical… more
- Daiichi Sankyo, Inc. (Bernards, NJ)
- …drug development plan, design, conduct, and interpret Phase 1 (specifically Clinical Pharmacology) studies, support Phase 2/3 studies, represent function on study ... of PK-PD and Pop PK-PD concepts and analysis, phase 1-4 clinical studies, literature, regulatory guidelines, and physiological/pharmacological aspects of the drug.… more
- Daiichi Sankyo, Inc. (Bernards, NJ)
- …immune disorders. Summary This position supports the strategy for driving global Clinical Study Start-Up activities for PV Safety Operations. This position develops ... Flow Plans and electronic data capture (EDC) Safety report outputs, reviews clinical study protocols and the Clinical Study Oversight Plan,day-to-day management… more
- Daiichi Sankyo, Inc. (Bernards, NJ)
- …Manager Grade level. This position is responsible for enabling the on-time delivery of clinical supplies across the DSI portfolio. This role as CSO ( Clinical ... streams with key service providers and working with internal departments to progress clinical supply projects. Every effort has been made to identify the essential… more
- Tris Pharma (Monmouth Junction, NJ)
- …Tris has an immediate opening for a full-time permanent Director/Senior Director, Clinical Quality Assurance. This is a hybrid position. Job Title commensurate with ... experience.SUMMARY:Reporting to the Chief Quality Officer the Senior Director of Clinical Quality Assurance provides strategic leadership and direction for … more
- Merck & Co. (Rahway, NJ)
- …Scientist) has primary responsibility for the planning and directing of clinical research activities involving new or marketed Oncology medicines. Our company's ... oncology medicines span all phases of clinical development (pre- clinical to post-licensure). The Director will manage the entire cycle of clinical … more
