Clinical Trial Specialist

1 day left

Location
England
Salary
Negotiable
Posted
04 May 2021
Closes
18 May 2021
Ref
2608ZL20
Contact
Zara Linehan
Hours
Full Time
Contract Type
Contract
Experience Level
Experienced (non-manager)

i-Pharm Consulting are seeking on behalf of a Top 10 Biotech a Clinical Trial Specialist to takes on the key role of Study Specialist. This includes contributing to supporting study matters that impact study timelines, quality and budget.

THE ROLE

  • Site pre-qualification and country specific feasibility
  • Organise translations
  • Assess and approve site/country specific documents and essential regulatory documents
  • Prepare Institutional Review Board (IRB) and Institutional Etichs Committee (IRC) applications and track until approved
  • Complete internal administrative tasks
  • Good knowledge of ICH-GCP Guidelines, international and local regulations
  • Update all Clinical Trial Management systems and submit all relevant documents to central files
  • Work well with team members and give support to more junior staff
  • Manage protocols and sites independently
  • Require Minimal Supervision by Manager
  • Manage activities related to Startup
  • Develop study specific documentation

LOCATION

  • London, UK

RATE

  • Excellent daily rate

EDUCATION REQUIREMENTS AND QUALIFICATIONS:

  • Educated to degree level (life sciences or nursing)
  • Previous experience in start-up activities for clinical trials
  • Ability to manage multiple and varied tasks
  • Strong computer skills including CTMS and Microsoft Office
  • Excellent verbal and oral English

ABOUT i-PHARM CONSULTING

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.

www.i-pharmconsulting.com

TO APPLY
If you would like to discuss this vacancy further, please call Recruitment Consultant Zara Linehan on +44 (0)20 3189 0470, or email lmcquade@i-pharmconsulting.com. If this role is not suitable, Zara is also available to discuss other possible positions or answer any general questions regarding your career and the current market.

KEYWORDS

Clinical Trial Specialist / CTS / Trial Specialist / Contract Research Organisation / CRO / Clinical / CTMS / Ethics / Submissions / EDMS / Pharmaceutical industry / Pharma / West London / London / Uxbridge / West Drayton / Hayes / Ickenham / Hillingdon / Contract / Freelance / Freelancing / Contracting

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