Regulatory Science Lead – Veterinary Referrals

European Medicines Agency; Amsterdam; On-site; EUR 49,000 - 50,000; Full time

Benefits offered by this job

Relocation assistance

Health insurance

Career development opportunities

Job summary

European Medicines Agency Amsterdam is seeking a Scientific Officer (Referral Procedure CVMP) to provide scientific, regulatory and procedural input on veterinary referrals. You will coordinate assessments, interact with EU authorities and support CVMP outputs, balancing stakeholder needs in a multinational setting.

The role requires a university degree in life sciences, at least two years in regulatory work, and strong analytical, communication and collaboration skills with fluency in English.

Qualifications

• University degree of minimum three years in Medicine or Life Science must be obtained by closing date.
• At least 2 years of experience in regulatory evaluation of medicines or interaction with EU authorities.
• Strong analytical ability and ability to translate scientific evidence into practical solutions.
• Proficiency in English; knowledge of another EU official language is beneficial.

Responsibilities

• Provide scientific coordination and regulatory support for veterinary referrals and CVMP outputs.
• Serve as contact for internal/external stakeholders; support CVMP rapporteurs and prepare assessment documents.
• Collaborate with CMDv on referral matters and implement CVMP outputs at national level.
• Provide updates to CVMP/CMDv and prepare content for EMA webpages.
• Interpret legislation and guidelines, identify risks, and deliver compliant CVMP outcomes within deadlines.

Skills

Regulatory affairs

Scientific writing

English proficiency

Regulatory evaluation

Stakeholder coordination

Education

University degree in Medicine or Life Science

Job description

European Medicines Agency Amsterdam is seeking a Scientific Officer (Referral Procedure CVMP) to provide scientific, regulatory and procedural input on veterinary referrals. You will coordinate assessments, interact with EU authorities and support CVMP outputs, balancing stakeholder needs in a multinational setting.

The role requires a university degree in life sciences, at least two years in regulatory work, and strong analytical, communication and collaboration skills with fluency in English.