Description
Senior Regulatory Associate - CRO Experience - Clinical Research Organisation - Up to £45,000 basic - UKSenior Regulatory Associate - CRO Experience - Clinical Research Organisation - Up to £45,000 basic - UK
Up to £45,000 per annum plus benefits
7% pension (non contributory)
Healthcare
Dental
Private Medical
Life Assurance
Life Insurance
Sickness cover
You will be joining a leading provider of pharmaceutical support services as a Senior Regulatory Associate. This company partners with life science companies to make medicinal products safer and more accessible for the consumer and through acquisitions; our client has grown from strength to strength. They handle both clinical and post approval work, however their speciality is clinical. Previous regulatory experience within a CRO is required and you will need a minimum of 2 years.
Key Skills/Requirements
B.Sc degree or the equivalent (desirable) in a scientific discipline
- 1 - 3 years' regulatory affairs experience
- Regulatory experience in the preparation and submission of CTAs, the applications for import licenses, and any reporting procedures, e.g, SAE reporting obligations and procedures.
- Very strong organization, planning and budget tracking abilities to handle potentially conflicting multiple portfolio projects.
- Excellent verbal and writing communication skills to collaborate with and discuss technical information and regulatory requirements with project teams and governmental agencies.
- Expertise with information management technology (e.g., archiving databases, document editing software, statistical manipulation of data).
- Ability to work effectively within designated project review periods.
The company are still continuing to grow and encourage applicants with strong career ambitions to apply for the position. The role can take you up to management level very quickly and working in a small to medium sized organization, you will get great exposure to many different projects
If this is of interest to you and you would like to find out more information on this position or any other regulatory affairs positions, please contact Amanda Edwards on or please email a.edwards(a)realstaffing.com