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Clinical Trial Associate required for initial 12 month contract role in Hampshire.

Our Global Pharma client is looking for a CTA/CPA with at least 12 months clinical research experience working as a clinical trial administrator within a pharma, biotech or CRO.

Main Duties:
Provide efficient clinical trials administrative support across Phase II - IV
Assist with accurate Clinical Trials Management System data entry and reporting
Assist with clinical document generation, review and revisions.
Attend study team meetings, responsible for production of internal meeting Agendas and Minutes in accordance with department best practices, under the supervision of the Study Manager
Creation and maintenance of tracking systems for deliverables not tracked in CTMS
Assist with clinical compliance to SOPs, procedures and regulatory requirements by actively requesting and accurately completing required forms and documents.
May accompany Study Manager on site visits and/or CRO meetings as^necessary (excluding review of study files).
Assist in co-ordinating effective communication between functions and with external vendors and investigational sites.
Prepare electronic documents to meet company standards, as required for regulatory^submissions and Clinical Study Report publishing.

Minimum Requirements:
Previous experience within a CTA role
Ideally a life sciences degree or equivalent (Not Mandatory)

Unfortunately we are unable to assist if you do not have the work experience stated above, and we will require candidates who can legally work and reside in the UK.

Please apply online or contact Michela on 01932 219 320 or email Michela@cslrecruitment.com