full time legal management senior

Job Details

Bionical Emas is the only CRO to combine Clinical Development, Early Access Programs and Clinical Trial Supply, delivering a unique, seamless approach to bring life-changing medicines to patients around the world.

With clients, staff and offices around the globe, we offer a varied and international experience.
Our clients range from smaller biotech’s to large global pharmaceutical companies, all with different needs and expectations. As a business, we have invested heavily in ensuring we have the systems, processes, and people, to deliver for the very varied requirements of our clients. The culture of Bionical Emas is friendly, flexible and supportive, where all staff are encouraged to grow, develop and exceed their expectations.

Main Responsibilities

  • Provide strategic and operational regulatory expertise and support
    to EAP department
  • Be the client point of contact for regulatory activities for multiple EAPs
  • Liaise with regulatory authorities on behalf of Bionical Emas and... clients as
    required
  • Line management of regulatory associate(s)

Key things we are looking for

  • Bachelor’s degree in a healthcare/science related subject
  • Extensive experience within a Regulatory Affairs function
    in the Pharmaceutical Industry
  • Knowledge of Early Access Program regulations an advantage
  • In-depth understanding of the drug development process
  • Excellent verbal and written communication skills

Make a difference

At Bionical Emas, we are committed to supporting our clients and our staff, so that they can bring life-changing medicines to patients around the world. Join Bionical Emas on our mission to make a difference

See something wrong with this listing?

Contact support