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, cosmetics and life sciences companies through complex regulatory landscapes.
Whilst part of a team, you will work independently. Aside from regulatory submissions, you will engage with clients providing regular updates and advice on projects. This is a great opportunity to further develop your regulatory knowledge and consulting skills.
Key Responsibilities
Assist in preparing and submitting regulatory documents for UK, EU and US markets mainly on medical devices
Support clinical trial processes, registries and Post-Market Clinical Follow-up studies
Research evolving regulatory frameworks to keep strategies cutting-edge
Provide updates, presentations and regular communication with clients across multiple time lines
Work alongside senior consultants to develop tailored compliance solutions
Requirements
A degree in Life Sciences, Pharmaceutical Sciences, Regulatory Affairs or a related field
An understanding of clinical trials, registries, and PMCF requirements
Experience liaising with regulatory authorities and clients and presenting detailed reports to them
Familiarity with global regulatory bodies and frameworks
Strong IT skills and attention to detail
Excellent communication and problem-solving abilitiesPark 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