- Merck & Co. (North Wales, PA)
- …studiesWork 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
- 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)
- …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
- 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
- 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 (Madison, 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
- 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
- AbbVie (Boston, MA)
- …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
- 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
- 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
- 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 (North Chicago, IL)
- …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 (Mettawa, IL)
- …on Twitter, Facebook, Instagram, YouTube and LinkedIn. Job Description Purpose The Assistant Director , Medical Affairs has a key role within the designated ... Therapeutic Area. Working under the leadership of the Scientific Director /Medical Director , this leader supports the development...regulatory , etc.) as they relate to on-going medical affairs projects. + Ability to work effectively in a… more
- Veterans Affairs, Veterans Health Administration (Indianapolis, IN)
- …performed is in a variety of laboratory disciplines, such as chemistry, hematology , coagulation, urinalysis, microbiology, serology, and blood bank. This is an open ... all reagents received in chemistry, blood bank, coagulation, and hematology before reagents are put into use. This includes...that is then presented to the supervisor or laboratory director to review/approve before reagents or supplies are put… more
- Veterans Affairs, Veterans Health Administration (Orlando, FL)
- …within the Medical Center, the VISN, and Department of Veterans' Affairs . Advances clinical pharmacy practice, pharmacy and medical center research, efficient ... include, but not limited to; Primary Care, Anticoagulation, Specialty ( Hematology /Oncology, Cardiology, Endocrinology, Neurology, Mental Health, etc.), Acute Care,… more
- Bristol Myers Squibb (Madison, NJ)
- …and other departments, including Commercial, Clinical Research and Development, Regulatory Affairs , Managed Care, Pharmacovigilance, Market Access, Statistics, ... Research and Development + Statistics + Translational Research + Regulatory Affairs including CMC- Regulatory +...7+ years of clinical experience: including specific expertise in hematology /oncology as well as, medical affairs or… more
