- Olympus Corporation of the Americas (Center Valley, PA)
- …to the Senior Director Medical Safety as a member of the global medical safety team. You must be adept at cultivating strong collaborative relationships across ... and effective manner. + Demonstrates experience staying engaged with worldwide clinical practice guidelines, safety requirements, and global Competent Authority… more
- CSL Behring (King Of Prussia, PA)
- …the clinical trial process.** **Experience in overseeing large and/or complex global clinical trials.** **Thorough knowledge of ICH guidelines/GCP and its ... days a week. You will report to the Senior Director , Head of Clinical Compliance & Specialty...applicability to all stages of the clinical development process** \#LI-HYBRID **Our Benefits** CSL… more
- Organon & Co. (Plymouth Meeting, PA)
- …five years working in Regulatory CMC, with progressive experience in leading global development -phase programs. **Preferred Experience and Skills** + The ideal ... **Job Description** **The Position** The Principal Scientist ( Director ) Regulatory Chemistry, Manufacturing and Controls is responsible for Regulatory Chemistry… more
- Teva Pharmaceuticals (West Chester, PA)
- …oversight and guidance, and managing resources for medical writing support in clinical research documentation used in drug development and product registration. ... to make a difference with. **The opportunity** The Medical Writing Manager in Global Regulatory Medical Writing is responsible for writing and editing clinical … more
- Organon & Co. (Plymouth Meeting, PA)
- …lead the preparation and submission of CMC dossiers for programs in clinical development , marketing applications and post-approval life cycle maintenance phases. ... for assigned products through the product lifecycle. + Lead development and execution of global product and...Skills** A candidate with experience in Regulatory CMC in clinical development , initial marketing application and post-approval… more
- CSL Behring (King Of Prussia, PA)
- …Programming. You are responsible for providing hands-on support and technical guidance on clinical study teams. The development of study and ad hoc output ... listings and submission packages. This individual will participate in the design, development and quality control process for SAS programs used to access, extract,… 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 ... submission. Provide statistical thought partnership for innovative study design and clinical development plans, including Go-No Go criteria and probability… more
- Bayer (Indianola, PA)
- …a real difference, there's only one choice. **YOUR TASKS AND RESPONSIBILITIES** As Marketing Director for CV Launch, you will serve as a key commercial lead in ... + Lead tactical marketing efforts, including campaign planning, product imagery development , key messaging, and launch readiness activities; + Support internal… 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
- Cardinal Health (Harrisburg, PA)
- **_What Security contributes to Cardinal Health_** The Cardinal Health Global Security teams are responsible for designing, developing, and implementing procedures, ... person should be practical, proactive, and innovative, to ensure the Global Security department's objectives and security industry best practices are communicated… more