- Merck & Co. (Rahway, NJ)
- …studiesWork closely with a cross-functional group of experts in commercialization, regulatory affairs , statistics, and manufacturing to manage clinical ... of clinical development, including study design, placement, monitoring, analysis, regulatory reporting, and publication.Specifically, The Senior Director May… more
- Daiichi Sankyo, Inc. (Bernards, NJ)
- …collaborate with RD leaders in Clinical Operations, Biostatistics and Data Management, Regulatory Affairs , and other RD functions to ensure effective delivery ... for managing the multiple Clinical Science Asset Leaders (CSALs) at the Senior Director level for each respective program. This Clinical Science (CS) Group Lead will… more
- Merck & Co. (Rahway, NJ)
- …studies;Work closely with a cross-functional group of experts in commercialization, regulatory affairs , statistics, and manufacturing to manage clinical ... cycle of clinical development, including: study design, placement, monitoring, analysis, regulatory reporting, and publication. Specifically, the Director may be… more
- Schrodinger (Cambridge, MA)
- We're seeking an **Associate Director of Regulatory Affairs ** with expertise in hematology and oncology to join our Early Clinical Development team in ... or Cambridge, MA. This hire will report to the Director of Regulatory Affairs and...the company's development and business goals + Experience managing regulatory affairs in hematology /oncology +… more
- BeiGene (Emeryville, CA)
- …expedited pathways where appropriate. The individual will have regulatory affairs and cross-functional influence within the hematology development portfolio ... **General** **Description** _:_ The Executive Director , Hematology North America Lead will...product. The incumbent will provide leadership, guidance and strategic regulatory oversight for the hematology portfolio ensuring… more
- Veterans Affairs, Veterans Health Administration (Indianapolis, IN)
- …The incumbent serves as a Medical Technologist within the Blood Bank, Hematology , and Coagulation sections of the Pathology and Laboratory Medicine Service at ... on all reagents received in Blood Bank, Coagulation and Hematology before reagents are put into use this includes...testing, parallel testing that is then presented to the director to review/approval before reagents/supplies can be put into… more
- AbbVie (North Chicago, IL)
- …+ Interacts with and influences other cross functional departments (eg Clinical Development, Regulatory Affairs , Medical Affairs ), as needed, to ensure the ... Executive Medical Director is responsible for the safety strategy for Hematology late-stage oncology portfolio, and to supervise, manage and mentor the safety… more
- Bristol Myers Squibb (Princeton, NJ)
- …MS or commensurate experience preferred **Experience Requirements** Significant experience in regulatory affairs (eg 3-5 years) **Key Competency Requirements** ... careers.bms.com/working-with-us . **Position Responsibilities** + Develop global and/or US regulatory strategy for Oncology products in development and through life… more
- J&J Family of Companies (Horsham, PA)
- Director , Real World Value and Evidence - Hematology - 2406205674W **Description** Johnson & Johnson is currently recruiting a Director , Real World Value and ... to innovative treatments is of utmost importance. As the Director of Real-World Value and Evidence at Johnson &...and dissemination plans for a key product in Janssen's Hematology portfolio. You will play a crucial role in… more
- AbbVie (Mettawa, IL)
- …US One Ven marketing team, international functions such as market access, medical affairs , regulatory , legal, health economics, public affairs , regulatory ... development and execution of the overall portfolio vision for Pan-Ven and Hematology , aligned with individual Brand Strategies Indications in Venclexta CLL (Chronic… more
- Abbott (Princeton, NJ)
- …operational performance. Our location in Princeton, NJ currently has an opportunity for a Director of Medical Affairs , Americas. The Director of Medical ... executives, and scientists. **What You'll Work On** + Reporting directly to the Sr. Director , Global Medical & Scientific Affairs (GMSA), Abbott Point of Care +… more
- AbbVie (North Chicago, IL)
- …including Clinical Development Operations, Clinical Development, Biostatistics, Pharmacovigilance, and Regulatory Affairs , to ensure the integration and accuracy ... are 2 job openings: Director , Data Management Operations (Solid Tumor), Director , Data Management Operations ( Hematology ). Office locations: Lake County, IL,… more
- Regeneron Pharmaceuticals (Tarrytown, NY)
- The Senior Medical Director , Clinical Sciences, Hematology provides clinical leadership and is responsible for all clinical deliverables within the assigned ... with the Clinical Development Plans (CDP); clinical components of regulatory documents/registration dossier and brand related medical information, clinical… more
- Bristol Myers Squibb (Madison, NJ)
- …and in their personal lives. Read more: careers.bms.com/working-with-us . The Medical Director , US Medical, Multiple Myeloma will report to the Senior Director ... the US Commercialization organization, WW Medical, Clinical Research and Development, Regulatory , Translational Development, and Market Access, and will lead the US… more
- AbbVie (San Francisco, CA)
- …strong medical and scientific principles, knowledge of compliance and regulatory requirements, AbbVie's customers, markets, business operations and emerging issues. ... of scientific content of protocols, Investigator Brochures, Clinical Study Reports, regulatory submissions and responses and other program documents. * May oversee… more
- BeiGene (San Mateo, CA)
- …and collaboration with functional area peers including Drug Safety, Quality Assurance and Regulatory Affairs , as well as thought leaders in order to meet ... The Associate Director (AD) Clinical Study Management leads both indirect...Consultants preferred + Therapeutic or medical knowledge preferred + Regulatory authority inspection experience a plus **Computer Skills:** Efficient… more
- AbbVie (Florham Park, NJ)
- …strong medical and scientific principles, knowledge of compliance and regulatory requirements, AbbVie's customers, markets, business operations, and emerging issues. ... of scientific content of protocols, Investigator Brochures, Clinical Study Reports, regulatory submissions and responses, and other program documents. *May oversee… more
- Bristol Myers Squibb (Princeton, NJ)
- …partners with senior leaders across Legal, Commercial, Medical, R&D, Global Drug Development, Regulatory , IT, Audit, Finance and HR to build and integrate one global ... with practices of and intersections between commercial sales, marketing, medical affairs , and market access organizations in the pharmaceutical industry. + Ability… more
- AbbVie (Irvine, CA)
- …United States. As a Digital Thought Leader Liaison (Digital TLL) specializing in Hematology , you will play a pivotal role in driving strategic direction through ... traditionally with internal cross-functional partners including sales, marketing, medical affairs , legal, compliance + Build out new cross-functional working digital… more
- Merck (Rahway, NJ)
- …+ Work closely with a cross-functional group of experts in commercialization, regulatory affairs , statistics, and manufacturing to manage clinical development ... of clinical development, including study design, placement, monitoring, analysis, regulatory reporting, and publication. **Specifically, The Senior Director … more
