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Job Details

Regulatory Clinical Trial Application Submission Manager

Company: Regulatory Professionals
Location: Buckinghamshire
Reference: J26050
Closing Date: 19 Jun 17
Type: Contract
Salary (£): On Application

Job Summary:

Clinical Research Associate (CNS) - Spain This globally recognised and well respected CRO seeks an experienced and motivated Clinical Research Associate to join their established team of individuals based in Spain.


Regulatory Clinical Trial Application Submission Manager \ Regulatory Affairs Consultant
Rate: Dependant on experience
Location: Buckinghamshire
Duration: 6 months

Regulatory Professionals have just registered a new Regulatory Affairs Contract role which will give you the stability of a contract role until the new year as well as 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?
If so please send your CV urgently to or call 0118 952 2797 to discuss.
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 an approx 6 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"e;s. (no line management)
*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:
*Clinical Trial Application submission experience
*3-4 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.
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,

Apply for this job: Regulatory Clinical Trial Application Submission Manager

Contact Information:

Address:  UK Office
3rd floor 33 Blagrave Street Reading
Tel:  +44 (0)118 9522 797
Website:  Visit Our Web Site

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