Regulatory Affairs Manager – Greece

About the role

iQVIA is looking for a Regulatory Affairs Manager for Greece, based in Athens or within commuting distance, as regular travel to Athens is mandatory. The role covers renewals, variations, post-market and market approvals and lifecycle management, submitted to the Greek Health Authority.

Key responsibilities

• Act as a Regulatory Manager on complex projects, with guidance from senior staff when appropriate.
• Write regulatory documents with minimal review by senior staff.
• Guide junior colleagues, give feedback on technical documents and support their training and development.
• Present to clients at bid defense meetings, by phone or in person, for regulatory deliverables as directed by senior staff.
• Write or propose revisions for new regulatory standard operating procedures and act as reviewer where assigned.
• Travel regularly to the Greek Health Authority in Athens.

Required profile

• Bachelor's or Master's degree in Life Sciences or a related discipline.
• At least 5 years of experience in post-marketing maintenance, lifecycle management and regulatory affairs on the Greek market.
• Knowledge of regulatory procedures in Greece, especially marketing authorization transfers and cross-functional dependencies.
• Good working knowledge of regional regulatory intelligence.
• Experience with regulatory strategy, documentation requirements, timelines and budgets for marketing authorization transfers (MATs) and publishing projects.
• Native Greek and full working proficiency in English.

Required skills

• Specific regulatory or technical expertise and ability to manage regulatory projects and deliverables on time.
• Strong communication and presentation skills, as this is a client-facing role.
• Ability to plan and deliver work while maintaining quality standards.

The stated annualized base pay range is 44,200 to 66,200 EUR, depending on qualifications, location and schedule; incentives, bonuses and other benefits may also apply.