Regulatory Affairs Associate

Our client, a global pharmaceutical company, is currently looking for a Regulatory Affairs Associate to join their team in Uxbridge.

This is a great opportunity to work for a pharmaceutical company who have created a centre of excellence and constantly focus on driving innovation and using cutting edge techniques in their science.

Key Responsibilities

• Contribute to the creation and submission of regulatory documents, particularly to those associated with clinical trials, and ensure these are presented in a timely manner to the regulatory agencies
• Assist with post approval activities, pre-MAA submissions and with the preparation of regulatory authority meetings
• Gather all regulatory documents needed for applications and ensure that a record of it is kept
• Guarantee that all procedures adhere to Regulatory guidelines

Requirements

• Previous experience in centralised Regulatory Affairs and Clinical Trials particularly within the pharmaceutical industry
• Great knowledge of drug development process
• Excellent communication and interpersonal skills

Park Street People Ltd is an Equal Opportunities Employer. We do not discriminate on the grounds of age, race, gender, disability, creed or sexual orientation and comply with all relevant UK legislation. We are acting as an Employment Business in relation to this role.