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In partnership with our client, a leading company in the Pharmaceutical Industry, we are currently recruiting a Medical Science Liaison for Lisbon.
Job Responsibility:
Act as a subject matter expert for pipeline products in preclinical and early-phase clinical stages and be acknowledged internally and externally as an expert
Identify potential high-impact medical research projects and publication opportunities
Develop and maintain relationships with KOLs to collaborate on research projects, advisory boards and peer-to-peer educational initiatives
Act as a key resource for scientific and clinical questions related to pipeline development and product lifecycle
Respond to questions from the healthcare community with integrity, compliance, and adherence to all legal, regulatory, and argenx guidelines, policies & procedures
Communicate key clinical and scientific findings from ongoing trials to relevant stakeholders, ensuring that the information is understood and accurately represented
Ensure medical accuracy of Medical Affairs activities, including advisory boards and scientific expert meetings, publications, scientific congress activities, medical education, medical information content and medical field programs
Requirements:
Previous experience as a Medical Science Liaison (senior profile >8 years)
Proven experience in Medical Affairs, including a hands-on medical field role, is mandatory
Can translate scientific or clinical data into high quality medical information
Scientific and customer-centric mindset with successful track record of delivering results that meet or exceed targeted objectives
Demonstrable experience with project management, proactive planning, priority setting, and securing alignment
Good understanding and working knowledge of the Local Health Care system & activities in relation to field-medical activities
Have competencies in delivering medical / scientific presentations
Ability to work collaboratively and effectively together within cross-functional teams and networks
Exercises good judgment on clinical, regulatory, legal, quality and technical related compliance issues
ensures compliance obligations are met across all areas of responsibility
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