submission procedures uk regulatory affairs jobs
1-10 of 66 jobs submission procedures uk regulatory affairs
Regulatory Affairs Manager - Office and Home Based in the South East - Contract Company Summary... Procedures and for the preparation and submission of the Clinical Trial Authorisation applications. You... the preparation of the scientific advice meetings with the Regulatory Agencies in the UK and other Member States... and prepare regulatory submission documentation for allocated products covering the EU Centralised Procedure
Experience: N/A
Contract: any
Regulatory Affairs Manager Regulatory Submissions Specialist Our client currently is a world leader... . RESPONSIBILITIES AND DUTIES: *Prepare Ethics committees and Regulatory Authorities submission package for initial... trial submission *Prepare Ethics Committee and Regulatory Authorities submission package for any future... bonus schemes in the UK, Pension and Healthcare Keywords: Regulatory submissions specialist, regulatory
North East - South Yorkshire
Salary: Salary to 40K
EU Regulatory Affairs Executive / Yorkshire / North East / Leading Pharma!Location:North East... By MRP, DCP & National procedures to UK, FRANCE, GERMANY, IRELAND as per Council Directive Annexure-1... regulatory affairs experience, & a very competitive salary is offered along with a performance related bonus... are a recruitment business dedicated to the pharmaceutical industry, specialising in Regulatory Affairs, Quality
Contract: Permanent
/ UK / Regulatory Affairs Associate / Executive / RA / Regulatory / Reg Affairs / Senior Reg Associate... , prepares and/or co-ordinates the submission of non-clinical, clinical and safety regulatory documentation... in development. Represents International Regulatory function at cross functional submission team meetings... in Regulatory Affairs. Experience representing Regulatory Affairs on cross functional teams is mandatory
Requirements: This position will report to the Director in International Regulatory Affairs (Hepatitis) and will be responsible for the preparation of regulatory submissions for investigational and commercial hepatitis medicinal products
East Anglia
Company: NonStop RecruitmentSalary: £30000 - £40000 per annum
REGULATORY AFFAIRS EXECUTIVE, CLINICAL (cta, impd) OUR CLIENT IS AN ESTABLISHED CLINICAL RESEARCH... FRUITFUL PROFITS AND BUSINESS As a regulatory Affairs Officer you will have full exposure to the lifecycle... of European Regulatory Affairs such as Variations, Renewals and Registrations. However, there will be a core... and pricing of projects for Regulatory Affairs in the company. R review and prepare regulatory submissions
Cambridge Cambridgeshire | Cambridge jobs
Company: NonStop RecruitmentSalary: £30000 - £40000 per annum
REGULATORY AFFAIRS EXECUTIVE, CLINICAL (cta, impd) OUR CLIENT IS AN ESTABLISHED CLINICAL RESEARCH... FRUITFUL PROFITS AND BUSINESS As a regulatory Affairs Officer you will have full exposure to the lifecycle... of European Regulatory Affairs such as Variations, Renewals and Registrations. However, there will be a core... and pricing of projects for Regulatory Affairs in the company. R review and prepare regulatory submissions
Contract: Permanent
Cambridgeshire
Company: NonStop RecruitmentSalary: £40000.00 p/a
REGULATORY AFFAIRS EXECUTIVE, CLINICAL (cta, impd) OUR CLIENT IS AN ESTABLISHED CLINICAL RESEARCH... FRUITFUL PROFITS AND BUSINESS As a regulatory Affairs Officer you will have full exposure to the lifecycle... of European Regulatory Affairs such as Variations, Renewals and Registrations. However, there will be a core... and pricing of projects for Regulatory Affairs in the company. R review and prepare regulatory submissions
West London / Heathrow (Home Based or Office)
Company: AXESSSalary: On Application
Visit us at www.---.co.uk Keywords: Regulatory Affairs / Clinical / Clinical Submissions / UK / Reg... . PRIMARY DUTIES Prepare Ethics Committee and Regulatory Authorities submission package for initial trial... submission Prepare Ethics Committee and Regulatory Authorities submission package for any future trial... process. Experience with submission to Ethics Committees and Regulatory Authorities Experience
Requirements: An opportunity has arisen to join one of Europe’s fastest growing Pharmaceutical Organisations. The role is for a Regulatory Submissions Specialist to join the Global Clinical Monitoring Team. The role will see you submitting clinical studies Phase I
South East
Company: Clinical ProfessionalsSalary: £Negotiable + Benefits
. RESPONSIBILITIES AND DUTIES: *Prepare Ethics committees and Regulatory Authorities submission package for initial... trial submission *Prepare Ethics Committee and Regulatory Authorities submission package for any future... bonus schemes in the UK, Pension and Healthcare Keywords: Regulatory submissions specialist, regulatory... affairs executive, regulatory affairs associate, Middlesex Hertfordshire Buckinghamshire Essex Surrey Kent
are a recruitment business dedicated to the pharmaceutical industry, specialising in Medical Affairs, Regulatory... . PRIMARY DUTIES Applies thorough knowledge of GCP/regulatory requirements to all aspect study preparation... files for more complex studies, and oversees the preparation and submission to archives of other study... and procedures, as needed QUALIFICATIONS / EXPERIENCE REQUIRED: Display sound project management skills
Requirements: As the Clinical Trials Manager you’ll be responsible for independently managing a number of studies of various complexity. You’ll also organize and manage multiple tasks related to clinical studies under while simultaneously ensuring study milestones are