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Clinical Trials Administrator / Clinical Site Specialist

Job Title: Clinical Trials Administrator / Clinical Site Specialist

Location: South East England (London, Hertfordshire, Buckinghamshire)

A new opportunity has arisen for a CTA / CSS at Opiant Pharmaceuticals a specialty pharmaceutical company developing products for substance use, addictive and eating disorders.

We are looking for a CTA / CSS to join our clinical trials team to assist in the development of our clinical trial programme. Opiant is a small but rapidly growing company offering progression opportunities as the pipeline grows.

Key Roles & Responsibilities:

  • Support the management and oversight of global clinical trials
  • Set-up and management of electronic trial master files
  • Review and control of clinical trial documentation
  • Oversight and tracking of trial progress
  • Resolve queries with trial sites
  • Tracking of invoices and payments for trials
  • Tracking contracts and site agreements
  • Assist with regulatory and ethics submissions and commitments
  • Assist with study start-up and investigator site identification
  • Develops and maintains strong working knowledge of regulatory guidelines and ICH-GCP

Job Requirements:

  • Educated to degree level or equivalent
  • Previous clinical research experience
  • Computer literacy
  • Excellent verbal and written communication skills with the ability to work well autonomously and within a multi-disciplinary team.
  • Willingness to work in a matrix and virtual team environment
  • Effective time management