-
BioNTech BioNTech is a Germany-based biotechnology company with U.S. offices in Cambridge, MA, Berkeley Heights, NJ and Gaithersburg, MD, that focuses on developing cancer therapeutics, including
-
to work with multiple researchers, technical staff, post-docs, and graduate/undergraduate students in an interdisciplinary environment; • Must be able to exercise judgment and discretion and to prioritize
-
coordinating all aspects of regulatory submissions necessary to support clinical trials, product registrations, and post marketing requirements and commitments Assist in the development of regulatory strategies
-
medical congresses, (e.g. ASHP, ASA, ASRA, AAOS); attend sessions and medical education symposia and provide summary reports Develop pre- and post-authorization payer dossiers and submissions to guideline
-
communication and engagement activities, and participation in internal post-congress debriefs. Cross-Functional Collaboration and Innovation Collaborate cross-functionally with medical affairs, clinical
-
: Interpret and apply relevant regulations and guidelines to assist in the creation and implementation of effective regulatory strategies. · Life-Cycle Management: Support pre- and post-approval
-
& Hematology. The two-year Takeda Global Medical Affairs Fellowship Program is designed to prepare post-doctoral scholars for rewarding careers in the biopharmaceutical industry. Through hands-on experience
-
Strategy team, will help prepare for launches and post-approval pull-through by partnering closely with the broader multi-functional USMA team including trade and distribution, pricing and contracting and 3
-
an understanding of industry practice, regulations and guidance that govern activities including clinical development and post-marketing research, HCP and patient interactions, scientific publications, field