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Regulatory Affairs Associate Director – Clinical Trials – Global CRO – Remote (EMEA) £negotiable, car allowance, bonus, pension, healthcare + various other benefits

You’ll direct, oversee and manage complex regulatory projects within a global CRO. You’ll ensure quality deliverables on time and within budget, ensuring that all project work is completed in accordance to SOPs.

The Company

This is fantastic opportunity to work for a global, market leading CRO in their regulatory team. Pioneers in human and data science, this CRO is at the forefront of clinical trials across multiple therapy areas.

  • Global CRO, one of the front runners in clinical trials
  • Covering multiple therapy areas (Oncology, Rare Diseases, GI, CNS being just a few of them)
  • Hugely successful company who have a consistent and exciting project pipeline
  • Highly supportive company, they’ll work with you and support you in achieving career goals

The Role

You’ll be leading and managing high profile, large scale regulatory projects across multiple products/therapy areas. You’ll be working cross functionally, liaising with stakeholders across the business, globally.

  • Manage large, complex projects involving several regulatory or technical deliverables and/or region,
  • Conduct risk analysis, management, and contingency plans, as appropriate
  • Provides strategic regulatory and/or technical consultancy on a variety of projects
  • Manage meetings with Regulatory Agencies;
  • Author and/or review a complete single service regulatory proposal and defend costs and timelines to clients;
  • Provide mentorship to junior colleagues and advise others on various regulatory documents


To apply for this role as Regulatory Affairs Associate Director – Clinical Trials our client is hoping for someone with the following skills and experience

  • Ample Regulatory affairs experience within a CRO
  • Pharma experience will be considered if you have clinical trials experience within pharma
  • Global regulatory knowledge
  • Project management skills
  • Strong stakeholder management skills

What should you do next?

This Regulatory Affairs Associate Director – Clinical Trials role is one not to be missed; it encompasses the opportunity to manage and lead high profile, complex regulatory projects. To discuss this Regulatory Affairs Associate Director – Clinical Trials role further or to find out about other Regulatory Affairs jobs I’m currently working on, please get in touch or hit apply to submit your current CV.

Unless otherwise stated, if applying for a job within the UK or European Union, you must ensure that you are already authorised to work there.

Carrot Pharma Recruitment Ltd acts as an Employment Business and an Employment Agency on behalf of our client in recruitment for this role.

Apply Now!

Job Consultant

Hayley Shayestehroo

Regulatory Affairs

Senior Consultant

01625 361072

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