- Eisai, Inc (Nutley, NJ)
- …is your profile, we want to hear from you. The Vice President/Head of Global Clinical Operations is a senior leadership role responsible for overseeing all aspects ... execution within a pharmaceutical or biotechnology company. This role ensures studies are conducted efficiently, within budget, and in compliance with regulatory… more
- Eisai, Inc (Nutley, NJ)
- …the medical affairs plan, including post-marketing research, medical education , research grants, medical advisory boards, and scientific communication/publication ... substantial experience in the pharma/biotech industry. OR a combination of equivalent education , deep subject matter expertise in relevant area along with a broad… more
- Merck & Co. (North Wales, PA)
- Job DescriptionThe Associate Vice President (AVP)/Section Head, Global Clinical Development, Pediatrics will focus on driving strategy, development, and life-cycle ... responsible for the design and medical monitoring of clinical studies .Supervises development of clinical documents including protocols, clinical study reports… more
- Merck & Co. (South San Francisco, CA)
- …into the earliest stages of target identification and validation, and executing clinical studies to evaluate the relevance of potential targets to human disease in ... strategies through cross-functional teams that provide line-of-sight from First-in-Human studies through clinical Proof-of-Concept.- This includes Experimental Medicine … more
- Merck & Co. (Chicago, IL)
- …for approved, in-development, and active Company-sponsored trials and/or investigator-sponsored research studies and serve as a role model for other field medical ... therapeutic expertise.Consistent adherence to field and corporate policies and Global Medical Scientific Affairs (GMSA) strategy, including field standard operating… 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 ... Franchise Teams, Regional Product Directors, affiliates, Public Affairs, and Medical Education to ensure value evidence programs are consistent with marketing… more
- Merck & Co. (Rahway, NJ)
- …Business, Clinical Development, Decision Making, Functional Expertise, Healthcare Education , Human Resource Management, Investigator-Initiated Studies (IIS), ... Job DescriptionThe Executive Director Pulmonary Hypertension, Value & Implementation (V&I), Global Medical and Scientific Affairs (GMSA) (referred to as EDMA) is… more
- Merck & Co. (North Wales, PA)
- …for approved, in-development, and active Company-sponsored trials and/or investigator-sponsored research studies . The RMSD serves as a role model for other field ... Interest (AOI) for the RMSD's specific therapeutic area.ResearchUpon request from Global Center for Scientific Affairs (GCSA),Initiates discussions with SLs and/or… more
- Eisai, Inc (Nutley, NJ)
- …is your profile, we want to hear from you. The Executive Director, Global Clinical Development resides within the Oncology at Eisai. This Executive Director will ... as well as the clinical execution and oversight of the associated studies being conducted globally. The Executive Director will champion transformational business… more
- Merck & Co. (Rahway, NJ)
- …policymakers, HTA/reimbursement agencies, and health systems globally.Types of studies executed include prospective and retrospective observational studies ... development of American Managed Care Pharmacy (AMCP) dossiers for US payers, and Global Value Dossiers for use by local subsidiaries in their HTA submissions. The… more
- Merck & Co. (North Wales, PA)
- …(V&I) Outcomes Research, position resides in the V&I organization, which includes Global Medical and Scientific Affairs as well as Outcomes Research, and will ... technology assessment (HTA)/reimbursement agencies and health systems globally.Types of studies executed include prospective and retrospective observational studies… more
- Merck & Co. (North Wales, PA)
- …Evidence (RWE) in Oncology.- -Position objectivesTo design and execute real-world evidence studies , designed to demonstrate the value of new products in support of ... inform and contribute to the value evidence plan and associated studies which demonstrate clinical, economic, and patient-centered value. The work will… more
- Daiichi Sankyo, Inc. (Bernards, NJ)
- …for cardiovascular diseases, under the Group's 2025 Vision to become a " Global Pharma Innovator with Competitive Advantage in Oncology," Daiichi Sankyo is primarily ... systems across the organization. This position ensures that all global systems, electronic records, validation processes, and regulated applications meet… more
- Merck & Co. (Rahway, NJ)
- Job DescriptionThe Global Clinical Supply (GCS) organization is accountable for managing the 'end-to-end' integrated clinical supply chain across the full Research & ... the downstream activities of clinical supplies for their assigned studies . -The primary function of the IM CSPM is...Operations etc.) as well as other organizations such as Global Clinical Trial Operations (GCTO) Regional colleagues and … more
- Daiichi Sankyo, Inc. (Bernards, NJ)
- …RD (Research Development), FMA (Field Medical Affairs), MIE (Medical Information and Education ) and global functions as necessary to create and implement ... for cardiovascular diseases, under the Group's 2025 Vision to become a " Global Pharma Innovator with Competitive Advantage in Oncology," Daiichi Sankyo is primarily… more
- Merck & Co. (Rahway, NJ)
- …for small, intermediate, and large molecules from preclinical toxicology studies to commercialization. -Our development teams ensure robust composition, primary ... to perform the above duties and to develop the above capabilities. Minimum Education Requirements :Ph.D. with 8+ years industry experience, MS with 10+ years, or… more
- Eisai, Inc (Exton, PA)
- …supply of DS/ADI for pre-clinical and phase I to phase III clinical studies , including the development of long-range planning and weekly production schedules. Be ... produce material for toxicology and phase I to III studies ), and in the late-stage processes at CMOs that...staff and infrastructure can support manufacture of materials for global clinical supplies. Finally, the individual will be responsible… more
- Daiichi Sankyo, Inc. (Bernards, NJ)
- …medicines to help people. Under the Group's 2025 Vision to become a " Global Pharma Innovator with Competitive Advantage in Oncology," Daiichi Sankyo is primarily ... Reports and Common Technical Document submission.ResponsibilitiesSupport audit program for clinical studies and vendors as applicable for the area of GxP audits… more
- Merck & Co. (North Wales, PA)
- …to demonstrate your advanced leadership and technical skills as part of a global , cross-functional team. You will build and coach your team in the development ... in Microsoft office or similar (Excel, PowerPoint, Word, Outlook, etc.) Education /ExperienceBachelor's Degree +9 years of pharmaceutical, clinical drug development,… more
- Merck & Co. (Rahway, NJ)
- …to ensure successful launches.Cross-Functional CollaborationStakeholder Engagement: Collaborate with global , marketing, sales, operations, market access, patient and ... enhance US Human Health and business unit capabilities.Qualifications: Minimum Requirements: Education : Bachelor's degree in Business, Marketing, Biotechnology, or a… more
