Darum lohnt es sich
ph3Job description /h3 pFor our client, a dynamic international biotechnology company focused on clinical-stage development, we recruit a: /p pSenior/Executive Medical Director - Clinical Development /p pLocation: Based in Basel, Switzerland / Remote model /p h3Responsibilities /h3 ul liLead Clinical Development: Provide clinical and general medical expertise throughout the entire development process, ranging from the clinical development plan and protocol development to study conduct, regulatory submission(s), and product launch. /li liProtocol Oversight: Provide expert input to clinical studies and oversee protocol development in collaboration with the partner’s global teams. /li liRegional Strategy: Take responsibility for protocols to identify region-specific operational issues for the territory and provide medical oversight of clinical projects where necessary. /li liCRO Management: Act as the medical monitor or provide oversight for CRO partners regarding medical queries and issues. /li liRegulatory Interaction: Provide medical expertise during interactions with regulatory agencies. /li liVendor Oversight: Oversee vendors as needed to ensure clinical studies successfully meet regulatory submission goals. /li liExternal Engagement: Attend investigator meetings and deliver clinical presentations as needed.
Proactively identify key investigators in the region to cultivate long-term collaborations, and recruit/manage a regional Clinical Advisory Board if needed. /li liRelationship Building: Establish and maintain appropriate collaborations and relationships with external scientific experts, thought leaders, and the general medical community. /li /ul h3Your Background /h3 ul liEducation: Medical Doctor degree or Master degree in a relevant therapeutic area. /li liTherapeutic Focus: Relevant areas include Non-oncology, CV, Immunology, Special, Obesity, CNS, Muscle, etc. /li liExperience: At least 5-10 years of experience in clinical development or a pharmaceutical medical function. /li liRegulatory Experience: Previous experience in IND/NDA submission and interacting with regulatory authorities is preferred. /li liSoft Skills: Good communication skills and presentation skills. /li liLanguages: Fluent in English (written and verbal). /li /ul /p #J-18808-Ljbffr
