Contract Senior Study Specialist

  • London
  • Contract

Contract Senior Study Specialist - Rare Disease - Biopharma

i-Pharm Consulting are currently working with biopharmaceutical company specialised in rare diseases who are seeking a Contract Senior Study Specialist to support the registration and approval of clinical development assets. This is an initial 12-month contract which offers a hybrid working model.


You will be involved in:

  • Supporting the country oversight, site feasibility assessment and site selection.
  • CRO oversight of EC related submission and approval activities
  • Oversight of essential documents for study life-cycle management
  • Oversight and management of essential documents in the Trial Master File (TMF)
  • Facilitating Screening Authorization Forms sign off and oversee tracking.


  • BA/BSc obtained in nursing, life /health sciences.
  • Rare Disease experience is highly sought after.
  • Strong experience within study management and execution
  • Drug Development and Study Design 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.


i-Pharm Consulting is a specialist Recruitment Company servicing the Pharmaceutical industry in the UK and Europe. We provide both permanent and contract staff to a wide range of Pharmaceutical, Medical Device, Biotechnology and Contract Research Organisations (CROs). i-Pharm has specific expertise in Clinical Research, Medical Affairs, Regulatory Affairs, Pharmacovigilance, Quality Assurance and Bioinformatics.

Aleksandra Brujic Recruitment Consultant

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