Das ist der Job
pul liLead clinical development.
Darum lohnt es sich
Provide clinical as well as general medical expertise throughout developments, from clinical development plan, protocol development through study conduct, regulatory submission(s) and product launch. /li liProvide expert input to the clinical studies and provide oversight of protocol development, in collaboration with partner’s global teams /li liResponsible for protocols to identify region-specific operational issues for the territory.
Where necessary, provide medical oversight of clinical projects /li liPerform as medical monitor or oversight for CRO partners on medical queries and issues /li liProvide medical expertise in interactions with regulatory agencies /li liAttend investigator meetings; deliver clinical presentations as needed /li liOversight vendors as needed to ensure successful clinical studies for regulatory submission goal /li liProactively identify key investigators in the region and cultivate long-term collaborations.
Recruit and manage regional Clinical Advisory Board if needed /li liEstablish and maintain appropriate collaborations and relationships with external scientific experts, thought leaders, and the general medical community /li /ul h3Qualification /h3 ul liMedical Doctor degree or Master degree of relevant therapeutic area /li liAt least 3-5 years of clinical development or pharmaceutical medical function experience /li liPrevious experiences in IND/NDA submission and interacting with regulatory authorities preferred /li liGood communication skills and presentation skills /li /ul /p
