Senior Regulatory Affairs Consultant – MAAs Global Acceleration Initiative

When our values align, there's no limit to what we can achieve.
 
At Parexel, we all share the same goal - to improve the world's 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 we're committed to making a difference.

We are seeking experienced Regulatory Affairs professionals to join our dynamic team in support of a global acceleration client initiative for late-stage phase III assets. This is an exciting opportunity to play a crucial role in accelerating time to filing and approval in Global Country Initiative (GCI), emerging markets, and non-EU markets.

Our global regulatory teams are well supported to prioritise our major markets filings and are targeting high quality simultaneous filings with Stringent Regulatory Authorities (SRAs)as well as rest of world markets. Our ambition is to accelerate the time for submission, approvals and accessing markets, and this role’s mission will be to help realise this ambition.

Key Responsibilities:

• Develop and implement global regulatory strategies for simultaneous marketing authorisation submissions

• Identify risks and mitigations to protect business interests and maintain timelines

• Lead detailed preparation of regulatory plans for individual country filings

• Lead global filing teams in generating country-specific datasets and updating core documentation

• Lead adaptation of core dossier contents for country submissions

• Coordinate filing teams for RTQ generation, provide strategic guidance to the global filing teams to address the regulators question and guide the team to prepare high quality responses.

•  Set up global filing team meetings, draft responses, coordinate reviews and approvals.

• Suggest and coordinate innovative regulatory procedures to increase acceleration opportunities

• Work closely with the local and regional regulatory leads on all aspects of marketing review and approvals.

• Manage routine MA maintenance activities as required

Qualifications and Experience:

• University degree in a life science industry

• 8-15 years of relevant regulatory affairs experience

• Extensive experience in preparing global filing plans for markets worldwide, and awareness of regulatory frameworks in all major markets globally

• Strong leadership skills and motivated, to support senior filing teams through marketing applications, overarching CMC, Clinical and Nonclinical.

• Familiarity with CPPs and timing for filings in various markets

• Proficiency in Veeva Vault and other regulatory systems

• Excellent communication and organizational skills

• Experience working within a regulatory matrix team in the pharmaceutical industry

• Fluent in English, written and spoken