Clinical Trials Administrator

Recruiter
Clinical Professionals Ltd
Location
East Horsley
Posted
31 Jan 2018
Closes
18 Feb 2018
Sector
Healthcare
Contract Type
Permanent
Hours
Full Time
Clinical Trials Administrator Our client, a large CRO with Offices across the EU and America, are seeking a CTA's from all levels. Due to continued expansion they have created a new position for a CTA / Clinical Trial Administrator to work from their UK office in Cambridge. Job title: CTA / Clinical Trial Administrator Location: Cambridge - suitable for someone residing in Cambridge, Colchester, Peterborough, Bedford, Thetford, Northampton, Harlow, Bury St Edmonds, Luton, Milton Keynes, Salary: To be discussed via telephone conversation Job role: The CTA will be involved in most activities in preparation for study set up, conduct and completing a clinical trial. The successful CTA will also administer, co-ordinate and maintain the logistical aspects of clinical trials. Experience required: - Set up and maintenance of the Trial Master File (TMF), Electronic Trial Master File (eTMF) & Investigator Site File (ISF) - Assist with Ethics/Regulatory Submissions - Quality check study documents - Develop and maintain study tracking tools - Process and track invoices Summary: This is an excellent opportunity to join a market leading Biotech company with a strong pipeline of products. They offer stable and progressive careers, excellent training and support. Clinical Professionals is the leading pharmaceutical staffing consultancy in Europe. Our dedicated Clinical Team has over 10 years' experience of placing clinical research professionals into positions within Pharmaceutical, Biotech, CRO, Charity and Academia organisations. We work with global market leaders as well as partnering with SME's and Start-up's. If you are on the market for a new challenge, please contact the team today. CTA, Clinical Trial Administrator, TMF, Trial Master File, Cambridge, Colchester, Peterborough, Bedford, Thetford, Northampton, Harlow, Bury St Edmonds, Luton, Milton Keynes, Electronic Trial Master File (eTMF), Ethics/Regulatory Submissions, CRO, Clinical

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