CMC Author, Senior Regulatory affairs Specialist

Senior Regulatory Affairs Specialist (CMC author) - Homebased in UK, Poland, Spain or Germany 

As a Senior Regulatory Affairs Specialist (CMC) you will be joining the world’s largest & most comprehensive clinical research organisation, powered by healthcare intelligence.

In this role, you will serve as a regulatory CMC author/writer, supporting a leading global pharmaceutical company.

Responsible for global CMC regulatory strategies and activities for a large Pharma portfolio through clinical development, market launch and product lifecycle management.

What you will be doing:

• Managing routine CMC authoring and submission activities for an assigned products or
  product portfolio to assure the preparation of high quality and compliant global
  regulatory submission.
• Maintains regulatory CMC dossier templates in alignment with current ICH and
  relevant regional regulatory requirements and standards
  Maintains a core source file management system to support all global plasma CMC
  submission activities.
• Keeps current on global global submission requirements, standards and formats.
• Assures an effective collaboration with Global Regulatory Affairs CMC Strategists,
  Global Manufacturing and Global Quality SMEs for the timely preparation and review
  of regulatory submission documentation.
• Acts as liaison with relevant regulatory operations teams (e.g, Publishing)
  Supports the development of efficient submission authoring and preparation
  procedures to assure timely completion of submission packages per business and
  regulatory timelines.
• Helps maintain relevant submission-related systems and trackers and assures that
  global CMC regulatory submission documentation is consistent in terms of content and
  alignes with the global dossier templates.
• Identifies country-specific submission requirements.
• Collaborates with Global Regulatory CMC Strategists to define detailed scope of
  submissions.
• Coordinates document review sessions to collate comments and corrections of drafted
  documents and prepares the documents for final approval for timely submission.

You are:

• A minimum of an undergraduate degree in a life-sciences discipline (or be a licensed healthcare professional).
• The role requires a demonstrated experience in global pharmaceutical/biotechnological drug development and knowledge of the global regulatory CMC environment.
• Experience in authoring and managing components of regulatory submissions.
• Knowledge of global regulatory requirements.
• Ability to use precedent and previous experience to develop innovative and flexible approaches to achieve development and commercial goals.

What ICON can offer you:

Our success depends on the quality of our people. That’s why we’ve made it a priority to build a diverse culture that rewards high performance and nurtures talent.

In addition to your competitive salary, ICON offers a range of additional benefits. Our benefits are designed to be competitive within each country and are focused on well-being and work life balance opportunities for you and your family.

Our benefits examples include:

• Various annual leave entitlements
• A range of health insurance offerings to suit you and your family’s needs
• Competitive retirement planning offerings to maximise savings and plan with confidence for the years ahead
• Global Employee Assistance Programme, TELUS Health, offering 24-hour access to a global network of over 80,000 independent specialised professionals who are there to support you and your family’s well-being
• Life assurance
• Flexible country-specific optional benefits, including childcare vouchers, bike purchase schemes, discounted gym memberships, subsidised travel passes, health assessments, among others

Visit our careers website to read more about the benefits of working at ICON: https://careers.iconplc.com/benefits

At ICON, inclusion & belonging are fundamental to our culture and values. We’re dedicated to providing an inclusive and accessible environment for all candidates. ICON is committed to providing a workplace free of discrimination and harassment. All qualified applicants will receive equal consideration for employment without regard to race, colour, religion, sex, sexual orientation, gender identity, national origin, disability or protected veteran status. If, because of a medical condition or disability, you need a reasonable accommodation for any part of the application process, or in order to perform the essential functions of a position, please let us know through the form below.

https://careers.iconplc.com/reasonable-accommodations

Interested in the role, but unsure if you meet all of the requirements? We would encourage you to apply regardless – there’s every chance you’re exactly what we’re looking for here at ICON whether it is for this or other roles.