As the Post-Approval Studies Manager, you'll lead our client's efforts in overseeing and driving the success of post-approval studies, ensuring compliance, high-quality data, and effective stakeholder collaboration. The role will have the opportunity to understand what's it like to post market for meds.
As the Medical Director, you will serve as the foremost medical representative in the country. You will be responsible for implementing both short- and long-term medical strategies derived from the global, regional, and IM (Innovative Medicines) teams, while forging impactful strategic alliances with healthcare communities and government bodies.
The position entails providing leadership and guidance to field service and repair center teams. You will play a key role in driving the achievement of business goals, overseeing commercial and operational activities. Collaboration with various departments such as Sales, Marketing, CS, Distribution, and RAQA will be crucial in this role.
The role will support hemophilia, new product launches, and support global clinical development programs in Taiwan, and is responsible for acting as an expert in the creation of the medical strategy and operationalization of the medical activities as a key member of the Brand Team. And build up external partnerships with KOLs.
Join a cutting-edge company developing life-changing protein/peptide therapeutics and lead formulation development from pre-clinical to clinical trials. Tackle complex formulation challenges for protein/peptide drugs. Design innovative delivery systems and manage projects from lab to manufacturing. Collaborate with a passionate team of scientists to revolutionize drug development and bring breakthrough treatments to patients.
responsible for building up the Taiwan RA foundation
The Regulatory Affairs Department obtains and maintains marketing approvals of responsible products in Taiwan. It ensures full local regulatory and company compliance and provides regulatory expertise to support clinical research, product launches, and business development so as to assist in achieving business growth and full compliance with legal requirements for pharmacovigilance regarding regulatory affairs' relevant responsibilities.
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