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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.
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Collaborate effectively with regional and global functions to maintain high professional and ethical standards.
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Build and strengthen scientific relationships with key medical experts, research institutions, and professional associations.
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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.
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Contribute to market access and reimbursement activities from a medical perspective.
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Ensure high-quality medical information services and timely reporting of safety and quality issues.
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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.
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Solid understanding of pharmaceutical regulations, compliance, and industry standards.
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Broad medical and scientific knowledge, ideally including CNS or specialty care areas.
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Strong strategic thinking and ability to manage multiple projects simultaneously.
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Excellent communication, presentation, and interpersonal skills.
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Native Hungarian and fluent English (spoken and written).
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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 CNS 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:

