Overview

Reference Number: JO-2102-463601
Clinical Study Start Up Specialist
Rate: £40,000 – 43,000
Job Type: Permanent
Location: Central London / West End

Clinical Study Start Up Specialist
Suitable Locations: London, Berkshire,
Surrey
Permanent
Salary: Up to 43,000 + Benefits

Remote working: Due to the current Covid19 situation, this role will be on-boarded remotely and will be home-based for the foreseeable future.

My client (a global Clinical Research Organisation) is looking for an experienced Study Start Up Specialist to join on a permanent basis. Reporting directly into a Senior Clinical Operations Manager, you will be joining a team of up to 20 Start Up Specialists dedicated to various Start Up activities on UK studies.

Experience Required:
– Minimum 18 months study start up experience working in the CRO environment
– Must have strong EC submission experience
– Advanced level knowledge and use or IRAS system/Amendment tool
– Strong written and communication skills
– Ability to multi-task with good time management skills
– Client focused approach

Key Responsibilities:
– Customize and review, site specific Informed Consent Forms (ICF) and customize and negotiate any amendments.
– Develop strategy to manage quality country specific and/or site specific documents or essential regulatory documents and amended regulatory documentation.
– Main point of contact for the generation of country/site plans and the Study Start Up queries
– Build relationships with investigators and site staff for the management of Qualification follow-up/ site issues, site training, supplies and investigator site file set up.
– Occasional attendance on Site Initiation Visits

If you are interested in this role then feel free to apply or email directly at ed.taylor@cpl.com

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