Contract Study Specialist

  • London
  • Contract

Contract Study Specialist

i-Pharm Consulting are currently working with biopharmaceutical company specialised in rare diseases who are seeking a Contract Senior Study Specialist to support the feasibility, design, and execution Phase 1-4 and post approval studies. This is an initial 12-month which offers hybrid working.

The role:

You will be involved in:

  • Developing and reviewing the study specific documentation
  • Supporting the management of regulatory document collection and the tracking for sites.
  • Ensuring the investigator payment e.g site set-up, pass-through processing, visit payment processing and funding processing
  • Manage and resolve site related issue
  • Contributing to Global Study Operations risks identification and mitigation's.


  • BS or higher in nursing, life/ health sciences is preferred
  • Experience in oversight of external vendors
  • Previous experience with Compliance and Quality
  • Rare Disease experience


  • Length: 12 months
  • Start date: ASAP.
  • Location: London (2 days in-office)
  • Hours: 37.5 p/w


If you would like to discuss this vacancy further, please call Aleksandra Brujic on +35312645159 or email If this role is not suitable, Aleks is also available to discuss other possible positions or answer any general questions regarding your career and the current market.

Aleksandra Brujic Recruitment Consultant

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