Regulatory Affairs Senior Executive - Clinical Trial Application

We are currently working with a growing Regulatory group working on a wide variety of products and therapy areas. They are currently seeking a professional with strong Regulatory Clinical Trial Application (CTA) experience to join their thriving team.

Location: Hertfordshire office or home based (or a mixture)

Type: Permanent - either Full time or Part time (both options available)

Salary: Competitive with a strong benefits package

·        You will be responsible for the preparation and submission of Clinical Trial Authorisations Applications (CTA) and Substantial Amendments to Competent Authorities throughout the UK, Europe and Globally.

·        Must have strong project management skills (e.g. planning, prioritization, management of timelines).

·        Be able to work self-sufficiently with strong initiative.

·        A graduate in relevant scientific discipline

·        Experience working with ethics committees would be a bonus.

·        Ability to work under pressure and achieve timely submission and regulatory approvals

·        Good computer skill

·        Opportunity for development and promotion for the right professional

For further information contact Natalie Jones on 0207 183 5059 or email natalie@linkfieldgroup.com