Regulatory Affairs Manager
- Employer
- Actalent
- Location
- United Kingdom
- Salary
- Extremely competitive rate which is negotiable for the right candidate
- Start date
- 6 Oct 2021
- Closing date
- 5 Nov 2021
View more
- Discipline
- Clinical Research, Clinical Operations, Regulatory Affairs
- Hours
- Full Time
- Contract Type
- Contract
- Experience Level
- Experienced (non-manager)
Job Details
An Amazing opportunity to work with a Global Leading Healthcare company!
They are looking for an experienced Regulatory Affairs professional to join their clinical trial submissions team in a crucial position as Regulatory Affairs Manager.
The key responsibilities of this role will be to:
- Act as a Regulatory Advisor on complex clinical trial projects
- Coordinate and oversee the clinical trial application (CTA) process
- Maintain and prepare core clinical trial dossiers in accordance to regulatory requirements
- Act as a project manager on stand-alone projects
- Strategically plan and oversee global country submissions for complex studies
- Provide mentorship to more junior colleagues
We’re looking to speak with any Candidates that have:
- 5+ years’ experience within regulatory affairs
- Good experience working on Clinical Trial Applications
- Extensive knowledge of regulations and guidance supporting clinical research and development
- Experience working in a role as a project manager
This is an initial 6-month contract with the potential for extension. The role is paying an extremely competitive rate and will be completely home-based, however some on-site visits are an advantage.
If this sounds like the ideal role for you, please send your CV to bshepherd@aerotek.co.uk If this does not sound like the right role for you but you know someone that could be right, please forward on a method of contact to this person and you could be eligible of a referral fee. Also, we have a variety of roles that could be of interest but might not be advertised due to NDAs so please do feel free to send over your profile and we will be in touch with relevant positions.
Regulatory Affairs
Clinical Trials (CTA)
CTA
Regulatory submissions
Regulatory Strategy
Pre approval
Company
About Actalent
Actalent connects passion with purpose. Our scalable services and talent solutions drive value and results and provide the expertise to help our customers achieve more. Every day, our experts around the globe are making an impact. We’re supporting critical initiatives in engineering and sciences that advance how companies serve the world.
Actalent’s global footprint and flexible delivery models ensure access to specialized talent where and when you need it. We promote consultant engagement through professional development and provide experiences to ensure continuous learning. Our people are the difference.
Our expertise spans capabilities in engineering including product and manufacturing, systems and software, construction management, environmental, architecture and civil; and power and utilities. We focus on sciences capabilities in laboratory sciences, healthcare, and clinical research.
Actalent is an operating company of Allegis Group, the global leader in talent solutions.
- Website
- https://www.actalentservices.com/en-gb
- Telephone
- +44 0 1344 383 100
- Location
-
Maxis 2 ,
Western Rd
Bracknell
Berkshire
RG12 1RT
GB
Get job alerts
Create a job alert and receive personalised job recommendations straight to your inbox.
Create alert