- CSL Behring (King Of Prussia, PA)
- …therapies that make a meaningful difference worldwide. Could you be our next Senior Director , Global Clinical Program Lead, Cardiovascular? The job ... and external expert contributions to strategy and design of the assigned clinical program (s). + Responsible for maintaining alignment across critical… more
- 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 ... the cross-functional CDT acting as the lead scientific expert for the clinical program , while ensuring appropriate functional representation in team discussions.… more
- Teva Pharmaceuticals (West Chester, PA)
- Sr. Director , Global Clinical Operations TA Head, Neuroscience Date: Nov 9, 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
- Pfizer (Collegeville, PA)
- … trial results. + Provides clinical support to the study team or clinical program in response to audits or inspections, including providing support as needed ... **Job Summary** The Associate Director , Clinical Development Medical Director...cardiology, obesity, endocrinology, nephrology etc.) + Extensive knowledge of clinical development, global and regional regulation, ICH/GCP,… more
- Pfizer (Collegeville, PA)
- … Director will work with other functional disciplines as needed (eg Clinical Operations, Global Clinical Leads/Medical Monitors, Biostatistics, Data ... **JOB SUMMARY** + The overall role of the Early Clinical Research Clinician/Clinician Scientist Associate Director is...of clinical trials data together with the Global Clinical Lead, Clinical Safety,… 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)
- …more IM clinicians on one or more clinical studies or across a clinical program **Job Responsibilities** + Autonomously and independently leads clinical ... **Job Summary** The Director , Clinical Development Scientist: + Is... clinical support to the study team or clinical program in response to audits or… more
- Pfizer (Collegeville, PA)
- **Senior Director , (MD) Global Development Lead, Early Development** **ROLE SUMMARY** + Support clinical trials and the development strategy for early ... cross-functionally within Pfizer Oncology, as well as represent the program with the external clinical community. +...a leader and a key contributor. + Has a global perspective and mindset, with the ability to work… 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
- Pfizer (Collegeville, PA)
- The Director , Regulatory Program Management & Submission...is viewed as a key leader on the GRST ( Global Regulatory Strategy Team). The Director , RPMSS' ... of Pfizer Oncology's regulatory strategic and operational deliverables. The Director , RPMSS serves as the regulatory program ...asset, as well as Partner Line plans for the program . Spans from Pre- Clinical to Loss of… 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)
- **SUMMARY** + Sr. Director , Oncology Scientific Communications reports to the Team Lead Scientific Communications within Pfizer Oncology Medical Strategy Management. ... the publication planning, writing, and dissemination of scientific data from clinical trials and research activities, ensuring a cohesive and impactful publication… 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
- Pfizer (Collegeville, PA)
- **Use Your Power for Purpose** This position is for a Senior Medical Director within the hematology program . This individual contributor position will be ... Guidance, Clinical Insights & Interpretation + Collaborates with the Global Development Team to create and refine development strategies. + Represents the… more
- Pfizer (Collegeville, PA)
- …a product's lifecycle. The SSRM Safety Risk Lead is accountable for the global medical safety management of Pfizer products and performs proactive signal detection ... Works with other Pfizer functions engaged in benefit-risk management (Regulatory, Quality, Clinical , Medical, Corporate Audit, etc) to enable one medical voice +… more
- Pfizer (Collegeville, PA)
- This position is for a Medical Director within the CDK4 program . This individual contributor position will be responsible for supporting clinical trial(s). ... The successful candidate should ideally have prior experience in clinical trials and supporting development programs. **ROLE RESPONSIBILITIES** Study-level … more
- Catalent Pharma Solutions (Malvern, PA)
- Director of Quality - Malvern PA Catalent, Inc. is a leading global contract development and manufacturing organization (CDMO) whose mission is to develop, ... 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
- 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