Regulatory Affairs Specialist
1 week ago
Park Street People Ltd is seeking a skilled Regulatory Affairs Associate to join their team in the pharmaceutical industry. This role offers an excellent opportunity to work with a global company that prioritizes innovation and cutting-edge techniques.
The successful candidate will be part of a remote-by-design team, with occasional travel required to key meetings. Prior EU experience is preferred for this position.
This role involves providing regulatory guidance across the EU region, ensuring timely approval and compliance with regulatory deadlines. Key responsibilities include:
- Developing and preparing high-quality regulatory documents to support clinical trials and medical products.
- Contributing regulatory expertise to enhance product development.
- Aligning product development with the company's business model and global regulatory requirements.
- Serving as a primary point of contact between the company and regulatory agencies.
To be successful in this role, candidates should possess previous experience in Regulatory Affairs and Compliance, particularly within the pharmaceutical industry. They should also have a proven background working on clinical trial applications (CTAs) and marketing authorisation applications (MAAs).
Candidates with exposure to Regulatory Affairs legislation and procedures, strong communication and interpersonal skills, and the ability to work independently are highly sought after.
CompensationThe estimated salary for this position ranges from £23.70 per hour (PAYE) to £31.13 per hour (Umbrella), depending on the payment structure chosen. This rate includes holiday pay.
Park Street People Ltd is committed to equal opportunities and adheres to all relevant UK legislation.
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