Offer summary

Qualifications:

Bachelor's degree in life sciences or related field is required., Minimum of 5 years of experience in regulatory affairs, preferably in the pharmaceutical or medical device industry., Strong knowledge of UK regulatory requirements and submission processes., Excellent communication and analytical skills are essential..

Key responsibilities:

Manage and prepare regulatory submissions to the UK health authorities.

Ensure compliance with all regulatory requirements and guidelines.

Collaborate with cross-functional teams to support product development and market access.

Provide regulatory guidance and support to internal stakeholders and clients.

About Worldwide Clinical Trials  Worldwide Clinical Trials is a leading full-service global contract research organization (CRO) that works in partnership with biotechnology and pharmaceutical companies to create customized solutions that advance new treatments. Our capabilities include bioanalytical laboratory services, Phase I-IV clinical trials, and post-approval and real-world evidence studies – all powered by our team members who bring their expertise and a collaborative, personalized approach to each clinical program. Anchored in our company’s scientific heritage, our dedicated therapeutic focus on cardiovascular, metabolic, neuroscience, oncology, and rare diseases, is applied to develop flexible plans and solve problems quickly for our customers. Our talented team of 3,000+ professionals spans 60+ countries, and embraces a culture of diversity, equity, inclusion, and belonging (DEI&B). We are united in cause with our customers to improve the lives of patients through new, innovative therapies. For more information on Worldwide, visit www.Worldwide.com.

Required profile