- Larimar Therapeutics (Bala Cynwyd, PA)
- …in the preparation of regulatory and clinical documents. In this role the Senior Director of Medical writing will apply in-depth knowledge of medical and ... consultants have significant expertise in discovery, nonclinical and clinical development, regulatory affairs , and the development of manufacturing processes… more
- Larimar Therapeutics (Bala Cynwyd, PA)
- …consultants have significant expertise in discovery, nonclinical and clinical development, regulatory affairs , and the development of manufacturing processes ... and scientific leadership and a participatory workforce committed to success.Position: Senior Manager/Associate Director , Technical Operations Supply ChainPosition… more
- Larimar Therapeutics (Bala Cynwyd, PA)
- …consultants have significant expertise in discovery, nonclinical and clinical development, regulatory affairs , and the development of manufacturing processes ... and scientific leadership and a participatory workforce committed to success.Position: Senior Manager/Associate Director of Drug Substance Manufacturing Process… more
- Larimar Therapeutics (Bala Cynwyd, PA)
- …consultants have significant expertise in discovery, nonclinical and clinical development, regulatory affairs , and the development of manufacturing processes ... Director , Quality, (Validation and Data Integrity)Reports to: Senior Director , QualityPosition Summary:The Sr. Manager/Associate Director… more
- Larimar Therapeutics (Bala Cynwyd, PA)
- …consultants have significant expertise in discovery, nonclinical and clinical development, regulatory affairs and the development of manufacturing processes ... development of CTI-1601 and other future pipeline programs.Position Summary:The Associate Director of Clinical Data Management will provide support for Clinical… more
- Genmab (Morrisville, PA)
- …and authentic is essential to fulfilling our purpose. The Role: The Senior Medical Director supports Oncology Clinical Devlopment. Responsibilities: Oversee ... advisory boards, patient advocacy groups), internal stakeholders (eg, Research, Safety, Regulatory , Medical Affairs , Commercial), and internal decision boards… more
- Teva Pharmaceuticals (West Chester, PA)
- Senior Director Regulatory Affairs CMC (Biologic Products) Date: Jun 13, 2024 Location: West Chester, United States, Pennsylvania, 19380 Company: Teva ... and new people to make a difference with. **The opportunity** The Sr. Director , Global Regulatory Affairs CMC is responsible to oversee and help develop … more
- J&J Family of Companies (Horsham, PA)
- …related study reports, abstracts, and manuscripts. * Responsible for working with the Senior Director , Strategic Lead, Rheumatology TA, as well as other ... Associate Medical Director , Rheumatology Therapeutic Area - Medical Affairs...credible relationships with thought leaders, medical directors, and key regulatory officials. * Provide subject matter expertise and function… more
- Merck (North Wales, PA)
- …placement, monitoring, analysis, regulatory reporting, and publication. **Specifically, the Senior Director may be responsible for:** + Providing scientific ... medicines span all phases of clinical development (pre-clinical to post-licensure). The Senior Director will manage the entire cycle of clinical development,… more
- Takeda Pharmaceuticals (Trenton, NJ)
- …to bring life-changing therapies to patients worldwide. Join Takeda as Associate Director , Global Labeling Lead where you will be responsible for the development ... alignment for other medium and/or high complexity products. Interface with Senior Management Cross-Functional Team (GLOC) + Coordinates the process to obtain… more
- Pfizer (Collegeville, PA)
- **ROLE SUMMARY** The Specialty Care Operational Excellence Director role is an integral member of the Global & US Medical Affairs Teams, and the Operational & ... Change Excellence Team. The Specialty Care Operational Excellence Director leads the development and implementation of key US Field Medical Leadership Team (FMLT)… more
- J&J Family of Companies (Spring House, PA)
- …quality monitoring & compliance, data management, global medical safety, biostatistics, regulatory affairs , clinical supplies unit, medical writing, clinical ... Director , Project Responsible Physician - Neuropsychiatry - 2406186566W...Committee (IDMC) and adjudication meetings as needed. + Assists Regulatory Affairs in determining requirements for any… more
- J&J Family of Companies (Trenton, NJ)
- …of the Johnson & Johnson Family of Companies, is recruiting for a Director / Senior Director , Clinical Rseearch Physician for **Late Development Oncology** ... partnership with the Compound Development Team (CDTL) and project management, global regulatory affairs , clinical pharmacology, health economics, and the disease… more
- J&J Family of Companies (Horsham, PA)
- Director , Medical Safety Officer, Solid Tumor Oncology - 2406194380W **Description** Johnson & Johnson, is recruiting for a Director , Medical Safety Officer, ... Officer (CMO), the Qualified Person for Pharmacovigilance (QPPV) Pharma, Senior Management, Health Authorities (HA), Prescribers and/or Patients. In compliance… more
- J&J Family of Companies (Horsham, PA)
- Director , Medical Safety Officer, Neuroscience and Ophthalmology - 2406186128W **Description** Johnson & Johnson, is recruiting for a Director , Medical Safety ... Chief Medical Officer (CMO), Qualified Person for Pharmacovigilance (QPPV), Senior Management, Health Authorities (HA), prescribers and/or patients. In compliance… more
- Takeda Pharmaceuticals (Trenton, NJ)
- …to bring life-changing therapies to patients worldwide. Join Takeda as Associate Director , Global Labeling Lead where you will be responsible for the development ... and alignment of the labeling strategy and labeling content. Interface with Senior Management Cross-Functional Team (GLOC) + In alignment with TAU/MPD Labeling Lead,… more
- Pfizer (Collegeville, PA)
- ** Director , US GI Franchise Leadership and Health Equity** This role will be responsible for leading strategy and execution against Leadership Initiatives across the ... and resources + Collaborate with key Pfizer stakeholders - including Commercial, Corporate Affairs , Public Relations/Comms, Access, Medical Affairs , and BAI - to… more
- University of Pennsylvania (Philadelphia, PA)
- …and wellness programs and resources, and much more. Posted Job Title Director , Clinical Research Operations (Department of Dermatology) Job Profile Title Director ... alignment with the University of Pennsylvania, GCP, FDA and all applicable regulatory bodies. The candidate must have a comprehensive understanding of clinical trial… more
- Organon & Co. (Plymouth Meeting, PA)
- …execution detail. + Advanced - Understands the R&D Business Model, including clinical/ regulatory /medical affairs /PV functions, and how it interfaces with key ... **Job Description** **The Position** The Director , Quality Management System (QMS) Governance, Quality Planning, and Risk Management is accountable to deliver and… more
- M&T Bank (Wilmington, DE)
- … to engage other Risk Departments, Internal Audit, Legal and/or Regulatory Affairs regarding interrelated risk issues impacting fiduciary, operational, ... activities throughout the enterprise for their assigned area of responsibility. The Senior Compliance Advisor will help develop, implement, and execute strategy of… more
