Global Medical Affairs Medical Director – Pipeline
argenx
full-time
Posted on:
Location Type: Remote
Location: Belgium
Visit company websiteExplore more
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
- 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
- Inclusive environment
- Equal consideration for employment without discrimination
- Opportunity to improve lives of people suffering from severe autoimmune diseases
- Access to first-in-class therapies
Applicant Tracking System Keywords
Tip: use these terms in your resume and cover letter to boost ATS matches.
Hard Skills & Tools
medical inputclinical developmentevidence generationmedical strategiesdata generation planinvestigator sponsored studiespublication strategiesmedical education strategiesdrug development processregulatory knowledge
Soft Skills
partnership buildingcross-functional collaborationcommunicationstrategic thinkinginsight generationleadershiporganizational skillsstakeholder engagementteamworkadaptability
Certifications
BScMSPhDPharmDRNMBBSMB.ChB