My client is a global Pharmaceutical company who are urgently looking for a Clinical Study Start Up Specialist to join their team on a 12 month, fixed term contract. Ideally you will have a proven track record as a CTA / Project Administrator, with experience in study start up activity (ethics submissions, feasibilities, contract negotiation etc). Please note this is a 5 day week full-time position and you will be based onsite at our client's HQ. This is an ideal opportunity for an experienced CTA who is looking to take on a more senior role outside of monitoring.
ROLE
- Assist in the management of site start-up activities for clinical studies
- You'll be the primary contact with investigative sites during start-up activities
- You'll work with investigative sites to collect required regulatory documents
Essential Requirements
- UK experience (essential)
- Other European experience (desired)
- Experience in contract negotiations, ethic submissions and be familiar with the green light package
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 Principal Consultant Andy Yaxley on +44 (0)20 3189 2296, or email ayaxley@i-pharmconsulting.com. If this role is not suitable, Andy is also available to discuss other possible positions or answer any general questions regarding your career and the current market.
KEY WORDS:
Lead CRA / Senior CRA / Study Associate / Clinical Project Leader / Clinical Research Associate / CRA / Clinical Research / Clinical Research Scientist / Clinical Project Director / Clinical Study Manager / CTA / Clinical Trial Administrator / Study Start Up / Ethic Submissions / Pharma / CRO / Senior CPM / Lead CPM / UK / England / Scotland / Wales / M4 / South-East / Middlesex / Berkshire / Surrey / Buckinghamshire