Your new company
A well-known global biotechnology company with a great reputation for science and innovation is looking to bring a contractor on a 6-month initial contract into their CMC team.
Your new role
You will come in as the Regulatory Operations Associate where you will support the CMC team managing the regulatory documentation in Veeva. You will be responsible for supporting them from an administrative point to ensure the data is tracked correctly and submissions can run smoothly. In this role you will be given the opportunity to get a better understanding of what is required for regulatory cmc submissions in global markets and learn from senior members of the team.
What you'll need to succeed
- You will need to have 4+ years of administrative background in the life sciences industry.
- Previous experience working with Veeva Vault is important in this role to hit the ground running.
- Experience in Regulatory Affairs for 1+ year.
- Must be able to travel to Cambridge 3 days per week**
What you'll get in return
This is a great opportunity for someone to gain exposure to the regulatory CMC space and work for an innovative biotechnology company. There is scope that the role could be extended.
What you need to do now
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 Julia Bowden, Recruitment Manager in Regulatory Affairs.