Regulatory Affairs Associate CTA

Your new company

This global biopharmaceutical company is looking for a Regulatory Affairs Associate on a contracting basis to join their established Regulatory Affairs team. This contract job is 3 days onsite in Cambridge or Uxbridge.

Your new role

As Regulatory Affairs Associate, you will prepare regulatory Clinical Trial documentation and manage submissions to global regulatory agencies. You will typically participate in process updates and/or other special projects related to clinical trials.

Another key role of the Regulatory Affairs Associate is to complete or provide support in the preparation of clinical trial regulatory submissions in line with the International Council for Harmonisation of Technical Requirements for Pharmaceuticals for Human Use (ICH) requirements, regional requirements, and scientific and company policies and procedures.

What you'll need to succeed

In order to be considered for this contract job as Regulatory Affairs Associate, you must have previous Regulatory Affairs experience and be able to demonstrate sound knowledge of regulatory CTA requirements and the role of regulatory affairs as these pertain to medicinal product clinical trials, including knowledge and understanding of ICH standards and varying regional requirements in the assigned markets

What you'll get in return

Flexible working options are available.

What you need to do now

For more information on this job or any other contract roles in Regulatory Affairs, please apply to this advert and ask for Victoria Dunlop

If you're interested in this role, click 'apply now' to forward an up-to-date copy of your CV, or call us now.

If this job isn't quite right for you but you are looking for a new position, please contact us for a confidential discussion about your career.