Regulatory Affairs Consultant - Global Asset Lead home or office based in various European locations
Regulatory Affairs Consultant - Global Asset Lead home or office based in various European locations
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Job Description
When our values align theres no limit to what we can achieve.
At Parexel we all share the same goal to improve the worlds health. From clinical trials to regulatory consulting and market access every clinical development solution we provide is underpinned by something special a deep conviction in what we do.
Each of us no matter what we do at Parexel contributes to the development of a therapy that ultimately will benefit a patient. We take our work personally we do it with empathy and were committed to making a difference.
Parexel are seeking a highly skilled International Markets Regulatory Affairs Expert to join our dynamic team! We are looking for an experienced Regulatory Affairs professional with a broad understanding of regulatory science and requirements across international regions particularly in emerging markets. The successful candidate will provide strategic guidance on regulatory submissions and lifecycle maintenance across international regions. If you are passionate about regulatory affairs and want to make a significant impact in the pharmaceutical industry we encourage you to apply.
This role can be home or office based is selected European locations.
Key Responsibilities:
Develop International Regulatory Submission Strategies for a wide variety of products/projects
Support Project Leads in optimizing strategies for specific submissions in local markets
Guide delivery teams in creating International dossiers
Identify and mitigate risks related to international submissions
Conduct regulatory intelligence surveys and provide objective assessments
Represent the company at health authority meetings and document discussions and agreements
Coach mentor and lead regulatory teams to ensure timely and quality delivery of objectives
Monitor and advise on key changes in the regulatory environment of International markets
Qualifications:
University Degree in a Scientific or Technical Discipline
Several years of experience in pharmaceutical regulatory affairs particularly in international markets
Broad background in pharmaceutical business and experience in various regulatory affairs areas (e.g. Global European International Marketing Company or health authority experience)
Strong project management skills
Excellent interpersonal and intercultural communication skills
Proficiency in local language and extensive working knowledge of English
Critical thinking and problemsolving skills
Required Experience:
Exec
Employment Type
Full-Time
