Main Responsibilities:
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Develop and execute the local medical plan in alignment with global strategies and partner objectives.
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Offer medical expertise to cross-functional teams, ensuring patient-centered and compliant activities.
-
Collaborate effectively with regional and global functions to maintain high professional and ethical standards.
-
Build and strengthen scientific relationships with key medical experts, research institutions, and professional associations.
-
Support clinical research initiatives, including investigator-sponsored studies and feasibility assessments.
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Provide medical review and approval of promotional and non-promotional materials.
-
Contribute to market access and reimbursement activities from a medical perspective.
-
Ensure high-quality medical information services and timely reporting of safety and quality issues.
-
Manage medical budget planning, resource allocation, and training for internal teams.
- Degree in Life Sciences (Medical or Pharmacist degree is preferred)
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Minimum 5 years of experience in medical affairs, clinical, regulatory, or pharmacovigilance roles within the pharmaceutical or biotech industry.
-
Solid understanding of pharmaceutical regulations, compliance, and industry standards.
-
Broad medical and scientific knowledge, ideally including infectology or specialty care areas.
-
Strong strategic thinking and ability to manage multiple projects simultaneously.
-
Excellent communication, presentation, and interpersonal skills.
-
Native Hungarian and fluent English (spoken and written).
-
Proficiency in Microsoft Office tools.
-
Willingness to travel for business purposes.
Should you be interested in the details of this vacancy feel free to leave a comment with your details or submit your CV for this role.
Main Responsibilities:
-
Develop and execute the local medical plan in alignment with global strategies and partner objectives.
-
Offer medical expertise to cross-functional teams, ensuring patient-centered and compliant activities.
-
Collaborate effectively with regional and global functions to maintain high professional and ethical standards.
-
Build and strengthen scientific relationships with key medical experts, research institutions, and professional associations.
-
Support clinical research initiatives, including investigator-sponsored studies and feasibility assessments.
-
Provide medical review and approval of promotional and non-promotional materials.
-
Contribute to market access and reimbursement activities from a medical perspective.
-
Ensure high-quality medical information services and timely reporting of safety and quality issues.
-
Manage medical budget planning, resource allocation, and training for internal teams.
Requirements of the Role:
- Degree in Life Sciences (Medical or Pharmacist degree is preferred)
-
Minimum 5 years of experience in medical affairs, clinical, regulatory, or pharmacovigilance roles within the pharmaceutical or biotech industry.
-
Solid understanding of pharmaceutical regulations, compliance, and industry standards.
-
Broad medical and scientific knowledge, ideally including infectology or specialty care areas.
-
Strong strategic thinking and ability to manage multiple projects simultaneously.
-
Excellent communication, presentation, and interpersonal skills.
-
Native Hungarian and fluent English (spoken and written).
-
Proficiency in Microsoft Office tools.
-
Willingness to travel for business purposes.
Should you be interested in the details of this vacancy feel free to leave a comment with your details or submit your CV for this role.

