- CSL Behring (King Of Prussia, PA)
- The Associate Director (AD), Biostatistics, leads the full scope of statistical contribution to a clinical development program. The AD provides statistical ... strategies for the clinical trials and regulatory submissions and is accountable for...experience or MS with 11 years of experience in drug development + Experience providing statistical leadership at compound/indication… 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 Clinical … more
- Lilly (Indianapolis, IN)
- …Delivery & Strategy_ + Deliver Early Phase material to meet toxicologic and clinical milestones. + Develop a global network of active pharmaceutical ingredient, ... better for people around the world. We are a global healthcare leader headquartered in Indianapolis, Indiana. Our employees...Overview:** We are seeking a veteran and visionary Sr. Director of Early Phase Chemistry to join our leadership… more
- ThermoFisher Scientific (Greenville, NC)
- …regulatory review and approval of promotional and non-promotional materials to ensure global compliance. + Manages global Clinical Trial Authorization ... decisions. + ** Clinical Trial Regulatory Responsibilities** + Develop and oversee global Clinical Trial Authorization (CTA) submission strategy. + Act as the… more
- Genentech (South San Francisco, CA)
- …will manage a group of Medical Directors/Medical Science Directors, providing exceptional clinical , scientific, and people leadership. In USM, we focus on broadening ... while making care more accessible and affordable for all. The Principal Medical Director / Medical Science Director drives and guides medical strategy and… more
- Lilly (Indianapolis, IN)
- …candidates to the clinic, as well as to design and support nonclinical and clinical studies, supporting global registration packages. * Lead R&D initiatives to ... regulatory documents (eg. IB, IND, IMPD, NDA/BLA, etc.) to support global regulatory submissions (including sections 2.6.4./non- clinical pharmacokinetics and… more
- Bristol Myers Squibb (Cambridge, MA)
- …apply our individual talents and unique perspectives in a supportive culture, promoting global participation in clinical trials, while our shared values of ... treatment we pioneer. Join us and make a difference. **Position Summary** The RWE Director is a key member of cross-functional teams and RWE-CoE within GBDS. This… more
- Organon & Co. (Plymouth Meeting, PA)
- **Job Description** **The Position** The role of Associate Director , Dermatology Outcomes Research Epidemiology and Economics will report to the headquarters ... Director of Medical Affairs Outcomes Research. Core elements enabling...and contracting. The role is responsible for evaluating the Clinical and Economic models that support the utilization of… more
- Gilead Sciences, Inc. (Foster City, CA)
- …with Global evidence generation partners - GMA / MAR, RWE, HEOR, Clinical Development, Global Publications, PSTs as needed + Facilitate sharing of best ... hundreds of thousands of people, a pipeline of late-stage drug candidates, and unmatched patient access programs to ensure...an exciting opportunity within US Medical Affairs for a Director , Portfolio Strategy in our Patient Access and Quality… more
- ThermoFisher Scientific (Middletown, VA)
- …Scientific team, you'll discover meaningful work that makes a positive impact on a global scale. Join our colleagues in bringing our Mission to life every single day ... our customers to make the world healthier, cleaner and safer. We provide our global teams with the resources needed to achieve individual career goals while helping… more