Senior Regulatory Affairs Specialist

4 weeks ago

London, United Kingdom ClinChoice Full time

Regulatory Senior Specialist
Are you interested in working directly for a single sponsor while having the security and additional career opportunities that working for a global CRO can bring? ClinChoice, is searching for an experienced Regulatory Senior Specialist to work with one of our Consumer Health partners, with a focus on over-the-counter (OTC) Pharmaceuticals. The Senior Specialist will be responsible for developing and supporting regulatory strategies for OTC drugs and ensuring compliance with regional and global regulatory requirements.


ClinChoice is a global full-service CRO with a strong focus on quality, professional development, and supportive culture. Develop and implement regulatory strategies for OTC pharmaceutical products to ensure timely approvals and compliance with regulatory requirements.
Prepare, review, and submit regulatory documents, including New Drug Application (NDAs), Abbreviated New Drug Applications (ANDAs) and Marketing Authorization Applications (MAAs).
Ensure compliance with regional and global regulatory standards, including FDA regulations, EMA guidelines and other relevant authorities.
Maintain accurate and up-to-date regulatory documentation and records. Prepare and submit annual reports and other regulatory filings.
Work closely with Research and Development, manufacturing, quality assurance and marketing teams to provide regulatory guidance throughout the product development and lifecycle processes.
Monitor and interpret regulatory developments, guidelines, and industry trends to inform internal teams and adjust regulatory strategies as needed.
Provide training and support to internal teams on regulatory requirements and best practices.

University Degree in Pharmacy, Chemistry, Biology, or a related field. Minimum of 5 years of experience in regulatory affairs within the pharmaceutical industry, specifically with OTC drugs.
In-depth understanding of regional and global regulatory requirements for OTC pharmaceuticals. Experience with FDA regulations, EMA guidelines and other international regulatory standards.
Ability to manage multiple projects and deadlines in a fast-paced environment.
Proficiency in Microsoft Office (e.g., Word, Excel, Outlook).

If you have the requirements we need, you will be invited for phone interview as the first step. ClinChoice is a global full-service CRO specializing in clinical development and functional solutions for pharmaceutical, biotechnology, medical device, and consumer health companies. We have over 28 years of proven high-quality delivery and results across all our services, with over 4,000 professionals in more than 20 countries across the Americas, Europe, and Asia-Pacific.
Our mission drives our culture: to contribute to a healthier and safer world by accelerating the development and commercialization of innovative drugs and devices. Our employees are the most valuable company asset and they are the fulcrum around which all ClinChoice activities are built and close management and training is the core instrument to develop and maintain highly-qualified personnel. The continuous training keeps the resources qualified in terms of competence and expertise and gives to all personnel the clear tools needed to manage both internal and client processes with the same methodology. We have based our success on attracting, developing, and promoting talent guided by diversity and inclusivity. Senior Regulatory Specialist, Regulatory Affairs, Reg Affairs, RA, Over the Counter, OTC, Consumer Health, CRO, Contract Research Organisation, Outsourced, Outsourcing, Sponsor-dedicated
#LI-EM1 #LI-REMOTE #Senior #FULLTIME #J-18808-Ljbffr

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