- CSL Behring (King Of Prussia, PA)
- …to developing therapies that make a meaningful difference worldwide. Could you be our next Director of Clinical Program , Immunoglobulins ? The job is in our ... CDT acting as the lead scientific expert for the clinical program , while ensuring appropriate functional representation...strategies \#LI-HYBRID **About CSL Behring** CSL Behring is a global biotherapeutics leader driven by our promise to save… more
- Teva Pharmaceuticals (West Chester, PA)
- Sr. Director , Global Clinical Operations TA Head, Neuroscience Date: Jan 6, 2026 Location: West Chester, United States, Pennsylvania, 19380 Company: Teva ... you'll spend your day** + Define and execute the global clinical operations strategy and oversee the...within the TA + Accountable for reviewing and approving clinical program /study budgets and long-term forecasting for… more
- Teva Pharmaceuticals (West Chester, PA)
- Director , Senior Counsel, Global R&D Compliance Date: Dec 10, 2025 Location: West Chester, United States, Pennsylvania, 19380 Company: Teva Pharmaceuticals Job ... people to make a difference with. **The opportunity** The Director , Senior Counsel, Global R&D Compliance role...This position will provide legal support for current Good Clinical Practice (GCP) and Good Laboratory Practice (GLP) quality,… more
- Organon & Co. (Plymouth Meeting, PA)
- **Job Description** **The** **Position** The Director , Clinical Pharmacology Lead will be responsible for contributing and/or devising the clinical ... while ensuring the scientific and data integrity, rigor and quality thereof. The director may represent the Clinical Pharmacology function in asset development… more
- Pfizer (Collegeville, PA)
- …and other functional lines for the successful implementation and execution of the clinical trial(s) within the assigned program . + Responsible for scientific ... technologies and adopts best practices aimed at improving the efficiency and quality of clinical development + Has a global perspective and mindset. Works well… more
- Pfizer (Collegeville, PA)
- …(POC) studies in Oncology. You will work in close collaboration with the Global Development Lead (GDL)and members of the development team to establish, lead, ... coordinate, and execute the early oncology clinical development plan(s). You will lead the development of...Digital Medicine). **POSITION RESPONSIBILITIES** + Partner closely with the Global Development Lead (GDL) in the execution of the… more
- Organon & Co. (Plymouth Meeting, PA)
- **Job Description** **The Position** We are looking for an experienced Associate Director , Program Manager to join our team. This successful candidate will ... provide program management expertise as an individual contributor to teams...Five years of industry experience in R&D functions (eg, Clinical Research, Early Development, Medical Affairs, Pharmacovigilance, Regulatory Affairs,… more
- CSL Behring (King Of Prussia, PA)
- …and Medical Writing, Director Medical Writing Processes & Standards Group Lead, Clinical Scientist Leads, Global Clinical Leads (GCL)s, and Clinical ... a meaningful difference worldwide. Could you be our next Director , Medical Writing Resourcing Group Lead? The job is...for the provision of medical writing services to support clinical development by way of managing the Medical Writing… more
- Pfizer (Collegeville, PA)
- **Job Summary** This position is for a Senior Medical Director within the atirmociclib program . This individual contributor will be responsible for supporting ... authority interactions and demonstrated leadership capabilities to ensure that the clinical development program meets scientific, ethical, and regulatory… more
- Teva Pharmaceuticals (West Chester, PA)
- …a difference, and new people to make a difference with. **The opportunity** The Director , in Global Regulatory Medical Writing, may write and edit clinical ... Director , Therapy Area Head, Medical Writing - REMOTE...for the direct medical-writing support in the production of clinical research documentation used in drug development and product… more
- CSL Behring (King Of Prussia, PA)
- …closely with Clinical Development and other key stakeholders. The Senior Director manages a team of statisticians both internal FTEs and external FSPs, and ... and clinical trials, ensuring robust methodology and alignment with program objectives. + Partner with Therapeutic Area (TA) leadership, Regulatory, Safety, and… more
- Pfizer (Collegeville, PA)
- **ROLE SUMMARY** The Director , AI & Data is responsible for directly overseeing and organizing wide-reaching Pfizer initiatives through digital-wide initiatives, or ... objectives and producing clear business-facing outcomes. This role reports to the Senior Director of AI & Data Enterprise Architecture which is responsible for the… more
- CSL Behring (King Of Prussia, PA)
- … (AD), Biostatistics, leads the full scope of statistical contribution to a clinical development program . The AD provides statistical strategies for the ... submissions and is accountable for the statistical deliverables within the program . ( Positions available supporting multiple Therapeutic Areas available ) Main… more
- Pfizer (Collegeville, PA)
- …a difference in the health and lives of millions of people. Pfizer, a global leader in the biopharmaceutical industry, is continuously seeking top talent who are ... Research & Development (R&D) Support and Services Lead for Clinical and Research is a member of the R&D...professional in one or more roles, such as Operations Director , systems engineer, support specialist, technology team lead, or… more
- Pfizer (Collegeville, PA)
- …**What You Will Achieve** This is a critical role requiring a strong Oncology Program Strategy Management Director ( Program Lead) capable of driving ... Program Strategy Management Group Lead. + The Program Lead will support Global and/or US...of the medical plan, working collaboratively with Oncology Early-and-Late Clinical Development, CMO, Safety, Oncology Regulatory Strategy, Global… more
- Teva Pharmaceuticals (West Chester, PA)
- …to make a difference with. **The opportunity** The Medical Writing Manager in Global Regulatory Medical Writing is responsible for writing and editing clinical ... and guidance, and managing resources for medical writing support in clinical research documentation used in drug development and product registration. **Travel… more
- CSL Behring (King Of Prussia, PA)
- …of Biostats. You will lead components of statistical contribution to a clinical development program . The Principal Biostatistician implements the statistical ... strategies for the clinical trials and regulatory submissions within the program...employee. **About CSL Behring** CSL Behring (http://cslbehring.com/) is a global biotherapeutics leader driven by our promise to save… more