- 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
- 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
- Merck & Co. (North Wales, PA)
- …studies;Work closely with a cross-functional group of experts in commercialization, regulatory affairs , statistics, and manufacturing to manage clinical ... talented and dedicated colleagues while developing and expanding your career.-- Director (Principal Scientist) has primary responsibility for the planning and… more
- Pfizer (Collegeville, PA)
- **ROLE SUMMARY** The Hematology Global Access Strategy and Pricing Director (GASPD) role directly impacts the ability to achieve business objectives on a global ... there is robust evidence available for the launch of hematology assets. The Hematology GASPD is expected...delivery and will collaborate seamlessly across GAV, Global Medical, Regulatory , Commercial, Clinical, Corporate Affairs and Country… more
- J&J Family of Companies (Spring House, PA)
- …functional area partners (eg, Translational research, Precision Medicine and diagnostics, Regulatory Affairs , Market Access, Clinical Development) to identify ... Director , Early Development Leader - Hematology ,...drug development, such as translational research, clinical studies, or regulatory interactions. + Familiarity with healthcare relevant datasets, such… more
- Bristol Myers Squibb (Trenton, NJ)
- …MS with general knowledge of pharmaceutical operations, ie, advocacy, medical affairs , clinical development, regulatory , commercialization, + Understanding of ... leading the strategic engagement plan for WWMH Professional Societies and Associations. Director , Professional Societies and Associations, WWMH: + Serves as the BMS… more
- University of Pennsylvania (Philadelphia, PA)
- …Posted Job Title Biospecimen Research Coordinator (CRC A/B) (Department of Hematology /Oncology) Job Profile Title Clinical Research Coordinator A Job Description ... projects and our biospecimen repository. This position will report to the Administrative Director of the TMMC and will work closely with the research team.… more
- University of Pennsylvania (Philadelphia, PA)
- …more. Posted Job Title Clinical Research Coordinator B (Department of Hematology /Oncology) Job Profile Title Clinical Research Coordinator B Job Description Summary ... for monitoring visits and audits, 5) Assist the TCE Project Manager, Program Director , and/or PI with preparing materials for reports, meetings, presentations, and … more
- CSL Behring (King Of Prussia, PA)
- …serious and often rare conditions. Could you be our next Senior Manager of Regional Regulatory Affairs ? This position is located in our King of Prussia PA ... is a Hybrid role. You will report to the Director , Regional Regulatory TA Lead. **RESPONSIBILITIES:** +...GRA NA representative for assigned projects to the Global Regulatory Affairs Strategy Team (GRAST) to provide… more
- CSL Behring (King Of Prussia, PA)
- …to treat serious and often rare conditions. Could you be our next Manager of Global Regulatory Affairs ? The job is located in the King of Prussia office. This is ... a hybrid position. You will report to the Regional Regulatory Therapeutic Area Director Lead. **Responsibilities:** +...Lead. **Responsibilities:** + You will plan, direct, and monitor regulatory affairs activities so we have the… more
- Bristol Myers Squibb (Trenton, NJ)
- …to both clinical trial and post-marketing safety. + Familiarity with regulatory guidelines. + Considerable Multi-Brand Medical Affairs and ... Read more: careers.bms.com/working-with-us . **Position Summary** The Established Brands Associate Director is responsible for strategy and execution of medical … more
- Bristol Myers Squibb (Trenton, NJ)
- …the efforts of the CNCs within their designated Region._ _W_ _orking with the National Director and VP of Hematology , the CNC Associate Director provides ... in their personal lives. Read more: careers.bms.com/working-with-us . **Associate Director , Clinical Nurse Consultant** _The Clinical Nurse Consultant (CNC)… more
- Merck (North Wales, PA)
- …+ Work closely with a cross-functional group of experts in commercialization, regulatory affairs , statistics, and manufacturing to manage clinical development ... cycle of clinical development, including: study design, placement, monitoring, analysis, regulatory reporting, and publication. **Specifically, the Director may… more
- CSL Behring (King Of Prussia, PA)
- The Associate Director of US Market Access - New Products will lead US value, access, pricing, and reimbursement strategy in preparation for the launch of several ... access strategy, reimbursement planning, and early account engagement. This Associate Director is responsible for developing and executing the market access… more
- J&J Family of Companies (Spring House, PA)
- …portfolio. + Work with multifunctional clinical teams (eg Study physician, translational research, regulatory affairs , CDx) to identify and implement end to end ... Director , Early Development Lead - Solid Tumor, Oncology...+ Excellent communication, interpersonal, and written skills **Preferred:** + Hematology / Oncology fellowship training + R&D experience at a… more
- Merck (North Wales, PA)
- …+ Work closely with a cross-functional group of experts in commercialization, regulatory affairs , statistics, and manufacturing to manage clinical development ... cycle of clinical development, including study design, placement, monitoring, analysis, regulatory reporting, and publication. **Specifically, The Director May… more
- Merck (North Wales, PA)
- …+ Work closely with a cross-functional group of experts in commercialization, regulatory affairs , statistics, and manufacturing to manage clinical development ... cycle of clinical development, including: study design, placement, monitoring, analysis, regulatory reporting, and publication. **Specifically, the Director may… more
