- 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: Dec 8, 2025 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
- 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
- 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
- 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
- Catalent Pharma Solutions (Malvern, PA)
- ** Director , Finance** **Position Summary:** Catalent, Inc. is a leading global contract development and manufacturing organization (CDMO) whose mission is to ... and technicians and the latest technology platforms at more than 40 global sites, Catalent supplies billions of doses of life-enhancing and life-saving treatments… more
- Veterans Affairs, Veterans Health Administration (Wilmington, DE)
- …policy determination and implementation; Has a major impact upon administrative and clinical policy, strategic planning; Affects global health care policy, ... Summary The Associate Director for Patient Care Services is the Chief...Team, who is involved in strategic planning, organizational assessment, program development, and the chief spokesperson for organized nursing… more
- J&J Family of Companies (Malvern, PA)
- …https://www.jnj.com/innovative-medicine **We are searching for the best talent for** ** Director , Head of Subcutaneous Platform Device Engineering in Malvern, PA.** ... **Purpose:** The Director , Head of Subcutaneous Platform Device Engineering, will lead...and proven ability to drive platform standardization, innovation, and global regulatory readiness. You will be responsible for: **Strategic… more
- Merck (West Point, PA)
- …**Sr. Principal Scientist - Device Technical and Engineering Lead (Sr. Director Equivalent)** Our company's Device Product & Process Development (DPPD) Team ... and risk management techniques to positively support and influence clinical and commercial combination product development and launches. **Principal… more
- J&J Family of Companies (West Chester, PA)
- …workflow changes. + Defines, maintains, and monitors metrics relevant to the Global Clinical Evaluation team's activities and adjacent teams/functions, providing ... time and subject to any necessary consultation processes. **Purpose** : The Program Manager, Scientific Operations reporting to the Director of Scientific… 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
- IQVIA (Wayne, PA)
- … research, public health, or related fields. \#LI-DNI IQVIA is a leading global provider of clinical research services, commercial insights and healthcare ... range of health and welfare and/or other benefits. IQVIA is a leading global provider of clinical research services, commercial insights and healthcare… more