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Regulatory Affairs Officer

Park Street People

Henley-on-Thames

On-site

GBP 80,000 - 100,000

Full time

28 days ago

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Job summary

An established industry player is seeking a Regulatory Affairs Officer to join their innovative team. In this pivotal role, you will assist in navigating the complex regulatory landscapes for pharmaceutical and medical device products, ensuring that life-changing innovations reach the market efficiently. Your expertise will help in preparing and submitting essential regulatory documents while supporting clinical trials and post-market studies. This role offers a unique opportunity to contribute to the compliance strategies of leading life sciences companies. If you are passionate about regulatory affairs and eager to make a difference, this position is perfect for you.

Qualifications

  • Degree in relevant field is essential.
  • Strong IT skills and understanding of regulatory frameworks required.

Responsibilities

  • Prepare and submit regulatory documents for UK, EU, and US markets.
  • Support clinical trial processes and develop compliance solutions.

Skills

Communication Skills
Problem-Solving Skills
Attention to Detail

Education

Degree in Life Sciences
Degree in Pharmaceutical Sciences
Degree in Regulatory Affairs

Tools

Regulatory Document Preparation
Clinical Trial Support

Job description

Are you passionate about regulatory affairs and eager to help life-changing medical products reach the market? Our client is looking for a Regulatory Affairs Officer to support their team in guiding pharmaceutical, medical device and life sciences companies through complex regulatory landscapes.

Key Responsibilities

  1. Assist in preparing and submitting regulatory documents for UK, EU and US markets
  2. Support clinical trial processes, registries and Post-Market Clinical Follow-up studies
  3. Research evolving regulatory frameworks to keep strategies cutting-edge
  4. Work alongside senior consultants to develop tailored compliance solutions


Requirements

  1. A degree in Life Sciences, Pharmaceutical Sciences, Regulatory Affairs or a related field
  2. An understanding of clinical trials, registries, and PMCF requirements
  3. Familiarity with global regulatory bodies and frameworks
  4. Strong IT skills and attention to detail
  5. Excellent communication and problem-solving abilities

Park Street People Ltd is an Equal Opportunities Employer. We do not discriminate on the grounds of age, race, gender, disability, creed or sexual orientation and comply with all relevant UK legislation. We are acting as an Employment Agency in relation to this role.

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