Team Administrator for Regulatory Affairs – Cambridge, East Anglia – £15.00 to £16.50 per hour – 12 month contracts
The Opportunity: Working as a Regulatory Affairs Administrator, you will be supporting all product registration activities and related product registration submissions throughout the world, in order that registrations are achieved in a timely manner in accordance with both regulatory and our client’s needs.
Skills and Experience:
- A basic understanding of role of Regulatory Affairs and regulatory requirements in clinical trials would be beneficial
- Any relevant experience within the pharmaceutical industry would be useful or a degree in a related subject
- You must be proficient in general IT systems (e.g. Microsoft Word and Excel), and experience with regulatory systems would be beneficial, but not essential
- Strong organisation skills with a strong attention to detail, with excellent verbal/written communication skills and engaging interpersonal skills are required
Role and Responsibilities:
You will be working as part of a team providing support and resource for administrative electronic and paper filing work to support the clinical trial activities of our client in the international market region. You will support the regulatory teams for proof reading of regulatory product documentation and support for regulatory submissions, usually under the supervision from more senior associates. You will also tasked with performing filing and data retrieval functions as directed or in conjunction with departmental Managers.
Applications: To learn more how you can join our client’s successful Regulatory Affairs Administrative team based in Cambridge as a Team Administrator; please call and speak with Edward Laing here in our London offices at ISR Recruitment on 0203 872 6600 or please send through a copy of your very latest CV for an immediate call back.