Regulatory Scientist- Clinical Trial Application Specialist
I am currently working with a top pharmaceutical company in Hertfordshire who is looking for a Regulatory Scientist to join them on a 6-month contract.
The company is looking for someone to be responsible for the regulatory management of UK CTAs for assigned products through national procedures. The role contributes to the UK affiliates success by enabling clinical research and maintaining the company’s licence to operate.
Some of your responsibilities include:
*Actively managing the UK CTAs of assigned products
*Acting as subject matter expert for the department in clinical trial related subject
*Complying with all regulations, industry codes and internal policies and procedures
*Contribute to efficiency and process improvement including development of best practices, SOP maintenance and tracking tools
*Ensure high quality regulatory submissions are prepared and submitted in a timely manner
*Demonstrates current knowledge of regulatory clinical trial procedures
*Assess technical/scientific content of proposed CTA submissions
The company is looking for someone who has:
*Experience in Regulatory Affairs, with working knowledge of EU/UK CTA management
*Able to manage multiple CTA submissions
*Must have clinical trial experience in the UK, including submissions and amendments
*Must know about MHRA/ health authorities in the UK
The company is ideally looking for someone who is able to start in September. If you are interested in finding out more about this role then please feel free to contact Sabrina Deo on 0121 616 3471 or firstname.lastname@example.org
Paramount Recruitment Limited provides services as an agency and an employment business. We regularly have similar roles in this area. Please see our website for details or send your CV in to us to find out the latest opportunities.
Job Reference: Sd-regscientist_1566475375
Broadcast As: 204
Salary To: Negotiable
Job Type: Full Time
Job Term: Contract
Recruitment Consultant: Sabrina Deo