Associate -Healthcare Regulatory

3 weeks ago


Reading Berkshire, United Kingdom CK Group- Science, Clinical and Technical Full time

CK Group are recruiting for a Regulatory Associate to join a biopharmaceutical company who are based in Reading on a contract basis for 12 months.

Out client is a global consumer healthcare business with well known household brands.

Coordinate Regulatory Life Cycle Management activities across multiple countries within and outside Europe.
Coordinate with Local Regulatory Affairs for variations, renewals and answering health authority requests.
Maintain Global Master Dossiers and compile, review, and provide dossiers for local registration and compliance to achieve variations for the specific product portfolio.
Ensure regulatory assessments are conducted for change controls in the respective Veeva Quality Tracking system.
Ensure that the Veeva Regulatory Information Management system is maintained and updated for all activities under role responsibility, including review of documents.
Provide strategic input into Regional Product labelling and approval to enable commercial activation of product launches.

Educated to ideally Masters’ degree level in pharmacy, engineering, chemistry or a similar field.
Regulatory affairs experience, preferably in consumer health and preferably across multiple regulatory classification areas
Experience of dossier maintenance and product change management as well as working with complex Regulatory databases
For more information, or to apply for this Regulatory Associate position please contact Mary Bolt on (phone number removed) or email (url removed).



  • Berkshire, United Kingdom Blackfield Associates Full time

    Are you looking to advance in your Pharmaceutical career? Do you have the knowledge and skills to oversee MHRA engagement? If so, I have the job for you! Offering £55k salary, bonus and benefits! As Regulatory Affairs Associate, you will: - Responsible for UK specific regulatory oversight on marketed products - Prepare and deliver regulatory...


  • Maidenhead, Berkshire, United Kingdom Planet Pharma Full time

    Role: Regulatory Affairs Associate Location: Maidenhead / M4 corridor. Salary: Very competitive salary on offer Planet Pharma are supporting a leading large global pharma company with the search for a new Regulatory Affairs Associate to join them during an exciting period of growth! Perfect for a junior regulatory professional with 6-24 months...


  • Maidenhead, Berkshire, United Kingdom Planet Pharma Full time

    Role: Regulatory Affairs Associate Location: Maidenhead / M4 corridor. Salary: Very competitive salary on offer Planet Pharma are supporting a leading large global pharma company with the search for a new Regulatory Affairs Associate to join them during an exciting period of growth! Perfect for a junior regulatory professional with 6-24 months...


  • Reading, Berkshire, United Kingdom IQVIA LLC Full time

    Associate Epidemiology Director page is loaded Associate Epidemiology Director Apply locations Reading, Berkshire, United Kingdom Rome, Italy Antwerp, Antwerp, Belgium Stevenage, United Kingdom Leeds, West Yorkshire, United Kingdom time type Full time posted on Posted Yesterday job requisition id R1419332 Associate Epidemiology Director IQVIA Real...

  • Regulatory Affairs

    1 week ago


    Maidenhead, Berkshire, United Kingdom Planet Pharma Full time

    Role: Regulatory Affairs Associate Location: Salary: Very competitive salary on offer Planet Pharma are supporting a leading large global pharma company with the search for a new Regulatory Affairs Associate to join them during an exciting period of growth! Perfect for a junior regulatory professional with 6-24 months regulatory experience! Manage...

  • Regulatory Affairs

    1 week ago


    Maidenhead, Berkshire, United Kingdom Planet Pharma Full time

    Role: Regulatory Affairs Associate Location: Salary: Very competitive salary on offer Planet Pharma are supporting a leading large global pharma company with the search for a new Regulatory Affairs Associate to join them during an exciting period of growth! Perfect for a junior regulatory professional with 6-24 months regulatory experience! Manage...


  • Reading, Berkshire, United Kingdom IQVIA LLC Full time

    Regulatory Manager, Clinical Trials Regulatory Management- Home-based, EMEA page is loaded Regulatory Manager, Clinical Trials Regulatory Management- Home-based, EMEA Apply locations Reading, Berkshire, United Kingdom Solna, Sweden Amsterdam, Netherlands Barcelona, Spain Sofia, Bulgaria time type Full time posted on Posted 7 Days Ago job requisition id...


  • Reading, Berkshire, United Kingdom IQVIA Argentina Full time

    Associate Epidemiology Director IQVIA Real World Solutions Home-Based/Hybrid/Office-Based This innovative epidemiologist role sits in the Center for Advanced Evidence Generation (CAEG) at IQVIA and reports directly to the Chief Scientific Officer. CAEG works alongside scientific teams across IQVIA and is responsible for driving innovation in...


  • Reading, Berkshire, United Kingdom IQVIA Argentina Full time

    Prepares and/or reviews regulatory documents to support clinical trial submissions. Independently provides regulatory support for more complex projects. Acts as a Clinical Trial Regulatory Manager (CTRM) on global projects which may be complex Ability to administratively and technically/scientifically review core scientific documentation and feedback gap...


  • Reading, Berkshire, United Kingdom IQVIA Argentina Full time

    Clinical Research Associate (all levels) Sponsor Dedicated, Home Based, UK Remote/Hybrid/Office based working options. Our Sponsor Dedicated (cFSP) team are growing, join us on our mission to drive healthcare forward! As Clinical Research Associate you will be responsible perform monitoring and site management work to ensure that sites are conducting...


  • Reading, Berkshire, United Kingdom IQVIA Full time

    join us on our mission to drive healthcare forward! We are recruiting for a Senior Clinical Research Associate to assist our sponsor’s Early Development team (phase 1). This is a fully remote position (open to candidates anywhere in the UK) with travel to sites. Professional development - resources that promote your career growth and programs to help...


  • Slough, Berkshire, United Kingdom Associate Clinical Educators Full time

    The Meducate Academy team line up during the 2-Day Cliniskills event dedicated to community pharmacists In September, Meducate Academy saw a surge in activity, notably due to our successful partnership with Cliniskills and participation in The Pharmacy Show. Out Associate Clinical Educators focused on teaching ENT and cardiovascular examinations to...


  • Reading, Berkshire, United Kingdom IQVIA LLC Full time

    Regulatory Manager, Clinical Trials Regulatory Management- Home-based, EMEA page is loaded Regulatory Manager, Clinical Trials Regulatory Management- Home-based, EMEA Apply locations Reading, Berkshire, United Kingdom Solna, Sweden Amsterdam, Netherlands Barcelona, Spain Sofia, Bulgaria time type Full time posted on Posted 7 Days Ago job requisition id...

  • Associate Temp

    1 week ago


    Reading, Berkshire, United Kingdom Project People Full time

    DATA PROTECTION ASSOCIATE - HYBRID - GLASGOW/READING Job Title: DATA PROTECTION ASSOCIATE - HYBRID - GLASGOW/READING DATA PROTECTION ASSOCIATE - HYBRID - GLASGOW/READING Data Protection Associate Glasgow or Green Park Reading (2 days/week in office, flex on days) Contract: 6 Months As part of the Data Protection team, the Data Protection...

  • Regulatory Specialist

    3 weeks ago


    Maidenhead, Berkshire, United Kingdom SRG Full time

    SRG are currently looking for Regulatory Specialist for a Global Pharmaceutical Company who have opened new vacancies within their Regulatory team on an initial 12 Month basis to be based at their office in Maidenhead/Remote. The Role: The Regulatory Associate is responsible for providing global regulatory expertise for Clinical Trials. They are the...

  • Regulatory Specialist

    4 weeks ago


    Maidenhead, Berkshire, United Kingdom SRG Full time

    SRG are currently looking for Regulatory Specialist for a Global Pharmaceutical Company who have opened new vacancies within their Regulatory team on an initial 12 Month basis to be based at their office in Maidenhead/Remote. The Role: The Regulatory Associate is responsible for providing global regulatory expertise for Clinical Trials. They are the...

  • Regulatory Specialist

    2 hours ago


    Maidenhead, Berkshire, United Kingdom SRG Full time

    SRG are currently looking for Regulatory Specialist for a Global Pharmaceutical Company who have opened new vacancies within their Regulatory team on an initial 12 Month basis to be based at their office in Maidenhead/Remote. The Role: The Regulatory Associate is responsible for providing global regulatory expertise for Clinical Trials. They are the...


  • Reading, United Kingdom G2 Legal Limited Full time

    **Corporate Associate Solicitor - Reading** Our client is one of the UK's leading full service law firms, with offices in Reading, London and the South East region. They provide clients with practical and straightforward legal advice whatever their regional, national and international requirements. Thefirm are seeking a Corporate Associate Solicitor 1-6...


  • Maidenhead, Berkshire, United Kingdom SRG Full time

    SRG are currently looking for Regulatory Specialist for a Global Pharmaceutical Company who have opened new vacancies within their Regulatory team on an initial 12 Month basis to be based at their office in Maidenhead/Remote. The Role: The Regulatory Associate is responsible for providing global regulatory expertise for Clinical Trials. They are the...


  • Berkshire, United Kingdom Cpl Full time

    Job Title: Regulatory Affairs Coordinator CTA, CTR (Consultant)Job Type: 12 Month Contract  Location: Berkshire, UK – Hybrid Rate: £22-25 per hour PAYE (inside IR35)We are partnered with a leading Pharmaceutical organisation who are looking for a junior Regulatory Consultant to join on a 12-month contract basis. This role will be sat in...