Regulatory Labelling Manager

hace 23 horas


Madrid, Madrid, España R&D Partners A tiempo completo

Shape global drug safety and compliance as a Regulatory Labelling Manager with a leading CRO consultancy.

R&D Partners is seeking a Regulatory Labelling Manager to join a leading consultancy in the CRO industry. This role focuses on regulatory affairs, particularly in labelling activities for innovator drugs on a global level. The position offers an exciting opportunity to contribute to lifecycle management and compliance within a dynamic and collaborative environment.

Please note that to be considered for this role you must have the right to work in this location.

Responsibilities:

  • Prepare, revise, and compile informative texts for healthcare professionals and patients (SmPC, PIL, Labelling) in EU and non-EU markets.
  • Develop target product-labelling profiles.
  • Manage creation and maintenance of CCDS, CCSI, RSI in collaboration with relevant departments.
  • Ensure communication of new and updated CCDSs and Product Information to internal and external stakeholders.
  • Escalate deviations and compliance issues to labelling governance bodies as necessary.
  • Handle labelling documentation and informative texts for innovator drugs globally.

Key Skills and Requirements:

  • Language Proficiency:
    Fluent business English or native English; additional EU language skills are a plus.
  • Educational Background:
    Degree in pharmacy, medicine, life sciences, or a bachelor's degree in science.
  • Regulatory Affairs Expertise:
    Proven experience in regulatory affairs with a strong track record in labelling activities for innovator drugs globally.
  • Lifecycle Management:
    Experience in handling marketing authorizations and their lifecycle management.

For more information, please contact
Henry LeLacheur
.

If you are interested in applying to this exciting opportunity, then please click 'Apply' or to speak to one of our specialists visit the 'Contact Us' page.

R&D Partners is a leading life sciences recruiter focused on finding exceptional people and matching them with the finest positions across the globe. R&D Partners is acting as an Employment Agency in relation to this vacancy.

By submitting this application, you confirm that you've read and understood our privacy policy, which informs you how we process and safeguard your data - https://www.r-

R&D Partners is seeking a Regulatory Labelling Manager to join a leading consultancy in the CRO industry. This role focuses on regulatory affairs, particularly in labelling activities for innovator drugs on a global level. The position offers an exciting opportunity to contribute to lifecycle management and compliance within a dynamic and collaborative environment.

Please note that to be considered for this role you must have the right to work in this location.

Responsibilities:

  • Prepare, revise, and compile informative texts for healthcare professionals and patients (SmPC, PIL, Labelling) in EU and non-EU markets.
  • Develop target product-labelling profiles.
  • Manage creation and maintenance of CCDS, CCSI, RSI in collaboration with relevant departments.
  • Ensure communication of new and updated CCDSs and Product Information to internal and external stakeholders.
  • Escalate deviations and compliance issues to labelling governance bodies as necessary.
  • Handle labelling documentation and informative texts for innovator drugs globally.

Key Skills and Requirements:

  • Language Proficiency:
    Fluent business English or native English; additional EU language skills are a plus.
  • Educational Background:
    Degree in pharmacy, medicine, life sciences, or a bachelor's degree in science.
  • Regulatory Affairs Expertise:
    Proven experience in regulatory affairs with a strong track record in labelling activities for innovator drugs globally.
  • Lifecycle Management:
    Experience in handling marketing authorizations and their lifecycle management.

For more information, please contact
Henry LeLacheur
.

If you are interested in applying to this exciting opportunity, then please click 'Apply' or to speak to one of our specialists visit the 'Contact Us' page.

R&D Partners is a leading life sciences recruiter focused on finding exceptional people and matching them with the finest positions across the globe. R&D Partners is acting as an Employment Agency in relation to this vacancy.

By submitting this application, you confirm that you've read and understood our privacy policy, which informs you how we process and safeguard your data - https://www.r-



  • Madrid, Madrid, España QualitecFarma A tiempo completo

    Regulatory Affairs ManagerSupervise and coordinate the execution of formulation, manufacture, dossier construction, registration of products. Also supervise the registration of companies, where applicable. Coordinate junior staff as and when required.Full TimeMadrid, SpainExperience required:At least 3 years in a similar work position.Duties required:Assist...

  • Regulatory Manager

    hace 2 semanas


    Madrid, Madrid, España Precision for Medicine A tiempo completo

    Precision for Medicine is not your typical CRO. At Precision for Medicine we have brought together new technologies, expertise and operational scale to help the life sciences improve the speed, cost and success rate of bringing life-changing therapies to patients. What sets us apart is the way we integrate clinical trial execution with deep scientific...


  • Madrid, Madrid, España Wise A tiempo completo

    Company DescriptionWise is a global technology company, building the best way to move and manage the world's money.Min fees. Max ease. Full speed.Whether people and businesses are sending money to another country, spending abroad, or making and receiving international payments, Wise is on a mission to make their lives easier and save them money.As part of...


  • Madrid, Madrid, España Wise A tiempo completo

    Company Description Wise is a global technology company, building the best way to move and manage the world's money.Min fees. Max ease. Full speed.Whether people and businesses are sending money to another country, spending abroad, or making and receiving international payments, Wise is on a mission to make their lives easier and save them money.As part of...


  • Madrid, Madrid, España Indero (formerly Innovaderm) A tiempo completo

    The Senior Regulatory Affairs Specialist will provide leadership for assigned projects regarding all regulatory activities that lead to startup of clinical trials and will oversee global/multinational complex large clinical trial submissions.This role will be responsible for sponsor-facing regulatory leadership and management of regulatory deliverables...


  • Madrid, Madrid, España Indero A tiempo completo

    The Senior Regulatory Affairs Specialist will provide leadership for assigned projects regarding all regulatory activities that lead to startup of clinical trials and will oversee global/multinational complex large clinical trial submissions.This role will be responsible for sponsor-facing regulatory leadership and management of regulatory deliverables...


  • Madrid, Madrid, España Indero A tiempo completo

    The Senior Regulatory Affairs Specialist will provide leadership for assigned projects regarding all regulatory activities that lead to startup of clinical trials and will oversee global/multinational complex large clinical trial submissions.This role will be responsible for sponsor-facing regulatory leadership and management of regulatory deliverables...


  • Madrid, Madrid, España OPIS A tiempo completo

    Due to our ongoing global expansion, we have a great opportunity for a Regulatory Submissions Specialist to join our growing regulatory team in Taiwan, on a fully remote basis.We are looking for someone who can autonomously carry on the work within the scope of their activities and interacts with the Direct Manager to define priorities and manages...


  • Madrid, Madrid, España IQVIA A tiempo completo

    Job OverviewDirect and manage the delivery of all required site activation, maintenance and regulatory activities for selected studies or multi-protocol programs, including pre-award activities, oversight of the scope of work, budget and resources.Essential FunctionsOversee the execution of Site Activation (including pre-award/bid defense activities) and/or...


  • Madrid, Madrid, España Abacus Medicine Group A tiempo completo

    Do you want to play a key role in ensuring compliance and smooth market access in pharmaceutical parallel trade? Join our Regulatory Affairs team and help us secure licenses and prepare packaging materials that put patient safety first.The opportunityAs ourSenior Regulatory Affairs Specialist in Spain, you will be responsible for obtaining and maintaining...