| London Jobs |
| Manchester Jobs |
| Liverpool Jobs |
| Nottingham Jobs |
| Birmingham Jobs |
| Cambridge Jobs |
| Glasgow Jobs |
| Bristol Jobs |
| Wales Jobs |
| London Jobs |
| Manchester Jobs |
| Liverpool Jobs |
| Nottingham Jobs |
| Birmingham Jobs |
| Cambridge Jobs |
| Glasgow Jobs |
| Bristol Jobs |
| Wales Jobs |
| Oil & Gas Jobs |
| Banking Jobs |
| Construction Jobs |
| Top Management Jobs |
| IT - Software Jobs |
| Medical Healthcare Jobs |
| Purchase / Logistics Jobs |
| Sales |
| Ajax Jobs |
| Designing Jobs |
| ASP .NET Jobs |
| Java Jobs |
| MySQL Jobs |
| Sap hr Jobs |
| Software Testing Jobs |
| Html Jobs |
| Job Location | Cambridge |
| Education | Not Mentioned |
| Salary | £16.00 per hour |
| Industry | Not Mentioned |
| Functional Area | Not Mentioned |
| Job Type | Temporary, full-time |
REGULATORY AFFAIRS ASSISTANT | 1 YEAR CONTRACT | PHARMACEUTICALSYour New CompanyA large research-based global biopharmaceutical company is looking for a Regulatory Affairs Assistant to join their team in Cambridge, UK. They are known for creating highly innovative medicines to improve the lives of patients with life-threatening diseases around the world. This role is within their therapeutic area, which focus on HIV/AIDS, liver diseases, cancer and inflammation, and serious cardiovascular and respiratory conditions. Your New RoleAs the Reg Affairs Associate you will be brought in to support the Reg Affairs therapeutic area team. Your support duties will include: supporting regulatory submissions, supporting clinical trial activities through administrative tasks and paper filing, and supporting regulatory teams by proof reading and QA checks for regulatory products. You will be very organized as you will need to file and retrieve data as directed, as well as document tracking, indexing and retrieving information to the regulatory department. What you will need to succeedYou will have at least 1-2 years experience within a regulatory affairs role in a Life Science industry. You will have previous experience with proof reading, and strong organizational skills and attention to detail. You will have previous experience with Gap Analysis. To be successful you will be a quick learner, and be proficient in general IT systems, with previous experience with regulatory systems. You must have strong verbal and written communication skills be results oriented, and have good oral and written communication skills. You will have a bachelors degree, a BTEC (or above), or have 2-3 years experience within a similar role. What you will get in ReturnThis is a 12-month contract position at their location in Cambridge. This role has the potential to go permanent. What you need to do nowIf you think this role may be suitable for you please click "apply now". Required skills
Keyskills :
Regulaty Affairs MHRA Pharmaceuticals Contract RA