My client, an independent Pharma business, has an exciting opportunity for a Regulatory Affairs Officer to join their team in Petersfield.
As Regulatory Affairs Officer, you will:
Assisting the RA department with Regulatory Affairs and Clinical Trial activities
Supporting on Technical Files and Dossiers
Controlling documents and ensuring compliance with GCP, EU GMP and any relevant regulatory body
Managing relationships with companies partnering CRO's and stakeholders
To be considered for the role of Regulatory Affairs Officer, you will:
Educated to degree level in a Science related discipline
Experience working with Good Clinical Practice is essential
Demonstrable experience with clinical trials of medicinal products or medical DevicesRandstad CPE values diversity and promotes equality. No terminology in this advert is intended to discriminate against any of the protected characteristics that fall under the Equality Act 2010. We encourage and welcome applications from all sections of society and are more than happy to discuss reasonable adjustments and/or additional arrangements as required to support your application.
Candidates must be eligible to live and work in the UK.
For the purposes of the Conduct Regulations 2003, when advertising permanent vacancies we are acting as an Employment Agency, and when advertising temporary/contract vacancies we are acting as an Employment Business
- Clinical Trials
- Good Clinical Practices (Gcp)
- Regulatory Compliance
- Stakeholder Management