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Job Details

Regulatory Clinical Trial Application Submission Manager

Company: Regulatory Professionals
Location: Buckinghamshire
Reference: J26050
Closing Date: 05 Jan 17
Type: Contract
Salary (£): On Application
Benefits:

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.

Requirements:

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 aman@regulatoryprofessionals.com 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
RG1 1LG
England
Tel:  +44 (0)118 9522 797
Website:  Visit Our Web Site

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