TITLE: Regulatory Affairs Clinical Data Co-ordinator
DEPARTMENT: Regulatory Affairs
REPORTS TO: Regulatory Affairs Clinical Data Manager


The role

Biocomposites continues to experience dramatic growth, realising our mission to increase the number of patients we can help, by extending our market coverage in new specialities and new geographies.

The Regulatory Affairs Clinical Data Co-ordinator is responsible for providing resource for regulatory activities relating to clinical data and post market data. In the role you will maintain awareness and support colleagues regarding regulatory status` of products in relevant countries.


What do we offer?

Competitive salary and benefits! With us, you will receive a competitive salary package and benefits.

We grow talent. At Biocomposites we create opportunities to thrive and grow.

One Biocomposites – team spirit & engagement. Our culture is important and we strive to create engaged and inclusive global teams that encourage colleagues to share their diverse perspectives and opinions.


Who do we look for?

People who are passionate about what we do.

People who are open minded to evolving the way we work.

People who can work together to transform outcomes and change lives.


Required experience:

  • Bachelor’s Degree in a life science or medical field.
  • Facilitating the generation of clinical data for post market requirements.
  • Ability to review and appraise disparate information into comprehensible reports.
  • 2 years’ experience in a post-market role in regulatory affairs.
  • Data analysis and critical evaluation.
  • Organisational skills and an ability to work to tight timelines.
  • Exceptional team working skills.
  • Experience of working with medical device regulatory bodies.
  • Proficient in the use of Microsoft Office.
  • Excellent communication skills when liaising within the company and with external customers.


If you are interested please forward your CV and cover letter stating the position you are applying for to careers@biocomposites.com