Medical Director, Pipeline
argenx
full-time
Posted on:
Location Type: Remote
Location: Switzerland
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Job Level
About the role
- Provide expert medical input to guide clinical development, comprehensive evidence generation, launch planning and brand plan execution in relevant indications
- Develop and execute ambitious short-term and long-term medical strategies, as key elements of the integrated data generation plan and brand plan
- Accountable for the alignment of all global medical affairs activities in partnership with other cross-functional members of the Indication Development Team
- Develop close partnerships with regional and country medical affairs leads/teams, and the regional indication strategy teams and ensure all activities maximise cross-regional impact whilst enabling regional team empowerment and supporting local delivery
- Build and maintain close partnership with external experts, in collaboration with regional/country Medical Affairs teams, to bring insight to all activities
- Initiate and support high impact medical activities, such as advisory boards, congress symposia and medical research projects
- Drive the identification and development of productive collaborations including with healthcare organisations and experts, other important customers and stakeholders and professional organizations
- Support strategy development for investigator sponsored studies and assessment of proposals
- Partner with scientific communications to support development of publication and medical education strategies
- Develop and continuously maintain the highest scientific and medical expertise with relevant diseases and products and be acknowledged internally and externally as an expert
- Systematically capture, distil and proactively communicate insights and activities within argenx
- Ensure all medical affairs activities maintain the highest standards, comply with applicable pharmaceutical regulations, as well as argenx policies and procedures
Requirements
- Scientific, healthcare or medical degree (BSc, MS, PhD, PharmD, RN, MBBS, MB.ChB or equivalent)
- Substantial medical affairs experience, throughout the product lifecycle
- A strong understanding of the drug development process and launch planning
- Relevant drug development, therapeutic area expertise and existing external expert network is an advantage
- Robust knowledge of regulations and practices related to industry interactions with healthcare professionals
- Experience partnering with regional/country and global functions and leadership
Benefits
- Equal consideration for employment without discrimination on the basis of race, color, religion, sex, sexual orientation, gender identity, national origin, protected veteran status, disability, or any other applicable legally protected characteristics
- Inclusive environment
Applicant Tracking System Keywords
Tip: use these terms in your resume and cover letter to boost ATS matches.
Hard skills
medical inputevidence generationmedical strategiesdata generation planmedical affairscollaborationsinvestigator sponsored studiespublication strategiesmedical education strategiesdrug development process
Soft skills
partnership buildingcross-functional collaborationcommunicationstrategic thinkinginsight generationempowermentleadership
Certifications
BScMSPhDPharmDRNMBBSMB.ChB