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CTS II: An award-winning CRO is looking for a clinical trials specialist with experience in clinical site initiation. This is a challenging and varied role that will require a talented start-up specialist to carry out a range of activities including trial submissions, ethics and inform consent whilst liaising with global clinical divisions. Ideal for an enthusiastic start-up specialist who is looking to further their career at an outstanding CRO.
The client is one of the top five CROs in the pharmaceutical and healthcare industry. They have an impressive global presence with offices in 50 countries and on-going clinical studies in over 100 countries. You will be given the chance to cover a broad spectrum of therapeutic areas from Phase I studies through to Phase IV, with extensive support, training and development given to staff at all stages of their career.
As a CTS I your role will include:
· Full clinical submissions – ethics, inform consent
· Driving forward site activities
· Ensuring investigators/site contacts are happy
· Coordination with CRAs and clinical division
This role will require:
· CTA or Trials Coordinator – 1+yrs experience
· Life Sciences degree
· CRO or Pharma employment
· Excellent communication, organisation skills
Commutable locations: Office based – Middlesex, London, Berkshire, Buckinghamshire
Salary: £25k - £27k + benefits
Full job description and company details are available upon application, apply below. This position is being dealt with by Yasmin Dyer at meet, call on + 44 203 178 7488 or email directly at email@example.com to discuss in confidence.
Find out more about us at www.peoplewithchemistry.com
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