- Merck & Co. (Upper Gwynedd, PA)
- …and programs.In collaboration with internal teams and external partners, designs studies ; authors study protocols; and develops measurement questionnaires, case ... Job DescriptionThe Principal Scientist/ Director , Value & Implementation (V&I) Outcomes Research, position...report forms, data analysis plans, final study reports, scientific presentations, and publications. Responsible… more
- Formation Bio (New York, NY)
- …you will provide strategic input to and monitor the execution of clinical studies as a project physician .Your ability to understand and navigate the ... the team, based on your clinical development experience you will be responsible for providing medical input into our Business Development product assessment strategy… more
- J&J Family of Companies (Raritan, NJ)
- …every step of the way. Learn more at https://www.jnj.com/innovative-medicine **POSITION SUMMARY:** The Director , Study Responsible Physician (SRP) is ... leaders, medical directors, and key regulatory officials. **Supervision:** Senior study physician /Trial Clinical Leader **SUPPLEMENTAL INFORMATION** **Education… more
- J&J Family of Companies (Titusville, NJ)
- …championing patients every step of the way. Learn more at https://www.jnj.com/innovative-medicine The Study Responsible Physician (SRP) is responsible ... protocol, clinical trial materials including protocol training, content of clinical study reports and relevant documents for regulatory filings. The SRP provides… more
- J&J Family of Companies (Spring House, PA)
- …to Proof-of-Concept (PoC). The Director , TM, will function as a clinical lead/ study responsible physician on early development programs and trials. They ... and biomarker science) and a clinical study responsible scientist. The span of studies in...studies ) through Proof of Concept. Within TM, the Director will be part of the Translational Medicine Program… more
- Bristol Myers Squibb (Princeton, NJ)
- …their personal lives. Read more: careers.bms.com/working-with-us . **Job Title** Director , Early Clinical Development - Immunology **Functional Area Description** ... drives early clinical strategy, and the design, execution, and interpretation of studies to select the most promising drug candidates for later development.… more
- J&J Family of Companies (Raritan, NJ)
- …the Company. The Medical Director , Global Medical Affairs, known also as the Study Responsible Physician (SRP) is accountable for the medical and ... scientific oversight of assigned clinical studies within the Global Medical Affairs function. This role...Medical Affairs function. This role ensures the integrity of study design, execution, and reporting, and serves as the… more
- Pfizer (New York, NY)
- …+ Responsible for scientific leadership and execution of clinical studies and delivering on innovative clinical study designs, high quality ... You will lead and coordinate the development of multiple studies of novel biological and small molecules for first...operations and the project team, to meet enrollment and study delivery timelines. You will also work with other… more
- Bristol Myers Squibb (Princeton, NJ)
- …Read more: careers.bms.com/working-with-us . **Position Summary** This **Senior Director ,** **Immunology & Neuroscience (I&N), Medical Evidence Generation (MEG)** ... generation for the I&N portfolio (including Medical Affairs Sponsored studies [MAST], Clinical Research Collaborations [CRC], and investigator-sponsored studies… more
- Merck (Upper Gwynedd, PA)
- …programs. + In collaboration with internal teams and external partners, designs studies ; authors study protocols; and develops measurement questionnaires, case ... **Job Description** The Principal Scientist/ Director , Value & Implementation (V&I) Outcomes Research, position...report forms, data analysis plans, final study reports, scientific presentations, and publications. + … more
- Pfizer (New York, NY)
- …team in governance meetings and submissions, partners with/supports the Development lead/Medical Director regarding study and disease area strategy. + Author ... **POSITION SUMMARY** You will be responsible for scientific oversight, data integrity and quality...portfolio. **KEY RESPONSIBILITIES** + Clinical development expert for assigned studies maintaining current scientific and clinical knowledge in the… more
- Pfizer (New York, NY)
- …the US Senior Medical Director , mRNA Vaccines, the incumbent will be responsible for supporting all aspects of the development and execution of strategic medical ... moving forward. **ROLE RESPONSIBILITIES** **As the US Senior Medical Director , mRNA Vaccines, the incumbent will be responsible...assets. + Support the execution of epidemiology and RWE studies - both field studies involving primary… more
- CUNY (New York, NY)
- …the CUNY Overview, the Director of Facilities Planning and Operations will be responsible for but not limited to the following: + Consult with the COO to oversee ... Director of Facilities Planning and Operations - Facilities...offers an accelerated BS/MD degree (7-year program) and a Physician Assistant Master's Degree (27 months program). True to… more
- J&J Family of Companies (Titusville, NJ)
- …Clinical Team; supervises, develops and recruits junior medical staff + Molecule responsible physician ; Responsible for the oversite of medical ... health for humanity. Learn more at https://www.jnj.com/. **POSITION SUMMARY:** The Senior Director , Clinical Leader (CL) is responsible for development and… more
- Pfizer (New York, NY)
- …medical resources, congress, and digital platform content. **ROLES AND RESPONSIBILITIES** The Director will be responsible for the following, with specific ... prevent and treat disease. **ROLE SUMMARY** The Vaccines Medical Communication and Content Director will: + Report to the Team Lead within Pfizer Medical Content and… more
- Pfizer (New York, NY)
- **Medical Director , Late Development, Oncology** **ROLE SUMMARY** This position is for a Medical Director within the PD-1/VEGF bispecific program. This ... individual contributor position will be responsible for supporting late stage clinical trial(s). The successful candidate should ideally have prior experience in… more
- Pfizer (New York, NY)
- **ROLE SUMMARY** The Sr Director Rare Hematology Integration Lead is an integral member of the Global Medical Affairs Therapeutic Area team. The Rare Hematology ... Pfizer systems, and processes involved with MA evidence generation and is responsible for defining and executing the strategy and tactics for Rare Hematology… more
- Pfizer (New York, NY)
- **Use Your Power for Purpose** This position is for a Senior Medical Director within the hematology program. This individual contributor position will be ... responsible for supporting clinical trial(s) and lead subteams in...In this role, you will: Clinical Development Leadership on Study Teams and Development Subteams + Conduct medical monitoring… more
- Pfizer (New York, NY)
- …research projects. + Work across the organization and on multifunctional teams responsible for the development of early development assets (including Product Team). ... and management of clinical protocols and amendments, investigator brochures, clinical study reports, statistical analysis plan, and regulatory documents. + Provide… more
- J&J Family of Companies (Spring House, PA)
- …and bioanalysis. The individual contributor role (reporting to the Executive Director , Global Translational Safety) requires a well-rounded physician scientist ... States of America **Job Description:** Johnson & Johnson is recruiting for a ** Director , Clinical Translational Safety Lead** to be located in Spring House, PA;… more
