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Reference No: J18270

Regulatory Professionals have just registered a new Regulatory Affairs Contract role which will give you the stability of a long term position as well as the benefits of a highly competitive hourly rate.

Would you want to work for a business that is leading the breakthrough with a cure for Cancer?

Do you have extensive Clinical Trial Application Submission experience?

Regulatory Professionals are currently working with an industry leader in Pharmaceutical science organisations. My client is looking for a Regulatory Affairs Clinical Trial Application Submissions Manager / Regulatory Affairs Consultant to join their team on a contract basis with the opportunity for the contract to be extended.
To give you an idea most contractors who work with the business started with a 6 month contract and have been there for over 2 years.

This opportunity will give you the chance to work on a wide range of therapeutic areas such as including Oncology, Neuroscience, Immunology and Infectious Disease and this is a role not to be missed.

As the successful Regulatory Affairs CTA Manager / Regulatory Affairs Consultant you will be:
• Responsible for managing Regulatory Affairs CTA submissions (phase 1-4)
• Responsible for implementing the global CTA submissions strategy, throughout the lifecycle of the trial.
• Lead the team that will compile, publish and produce CTA's.
• Liaise and submit direct to Regulatory Affairs health authorities.

To be successful in this role the Regulatory Affairs Consultant must have the following type of experience:
• Extensive Clinical Trial Application submission experience
• 4+ years’ experience within Regulatory Affairs.

Opportunities to work for this business on a contract basis do not come about very often and therefore if you are interested please send your CV urgently to or call 0118 952 2797 to have a confidential chat about your search.

We also offer a referral scheme whereby, for any candidate referred to us (who secures a job) we will give you £250 in vouchers. Please forward any referrals to us via phone or email.

Keywords: Regulatory Affairs Consultant, Regulatory Affairs Contractor, Regulatory Affairs Freelance, CTA, Clinical Trial Applications, CTA, Buckinghamshire, Berkshire, M4 Corridor, M40, Pre Approval, Clinical, EU, National, Contract, 6 months, Global Pharma, OTC, Oncology, Infectious Diseases,

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