Closing Date: 16 Dec 16
Type: Full Time
Salary (£): 40,000 - 60,000
We are currently seeking for an energetic and motivated Regulatory Submission Specialist to join our clinical team and manage clinical trial application submissions in the European region on a permanent basis full or part time. This position can be performed partly from home.
We are a rapidly expanding high profile CRO in our clinical team in the areas of a variety of different therapeutic fields within our company. We are currently searching for an ambitious Clinical Research Associate with a combination of enthusiasm as well as commitment for the clinical research industry.
Additionally to the competitive salary we are offering a comprehensive range of benefits, an excellent working environment and career opportunities on a global scale.
In this sounds appealing to you, please contact Aine Uusvel from Meet via email email@example.com or via phone +44 203 019 5973. The applications will be handled with discretion.
As a Regulatory Submission Manager you will be responsible for the following tasks:
• Preparation, coordination and execution of regulatory submissions to assigned countries within Europe
• Interacting with regulatory agencies and Ethics committees in Europe
• Perform quality checks on submission documents and site essential documents;
• Prepare and approve informed consent forms
• Advise sponsors and vendors on changing regulations and compliance requirements
In this sounds appealing to you, please contact Aine Uusvel from Meet via email firstname.lastname@example.org or via phone +44 203 019 5973.
Ideally we are looking for the following skills and experience:
• University degree or a relevant certification
• At least one-year submission experience
• Experience preparing, reviewing, and submitting regulatory documentation
Full job description and company details are available upon application, apply below. This position is being dealt by Aine Uusvel at Meet, please call on +44 203 019 5973. You can also e-mail us directly at email@example.com to discuss in confidence.
Meet are good people who are great at recruitment. We’re proud to partner with the industries leading Pharmaceutical, Biotechnology, Medical Device, Marketing Communications and Contract Research Organisations (CROs) worldwide, helping them to find and secure the best global talent available. We pride ourselves on our open, friendly approach and are here to guide you through the recruitment process every step of the way.
Find out more about us at www.peoplewithchemistry.com
Associated Key Words: Regulatory Affairs, European Regulatory Affairs, Reg Affairs, RA, EU, Regulatory Submission Manager, Regulatory Affairs Manager, Strategy, Submission, CRO, Contract Research Organization, Munich, Germany, Bayern, Augsburg, Nuernberg, Regulatory Submission Coordinator
Euston Tower Levels 32-34 286 Euston Road London
|Tel:||+44 203 178 7488|
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