Clinical Trial Associate required for initial 12 month contract role in Hampshire. CSL 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…
View full details of this job online at: http://www.cslrecruitment.com/Clinical_Trial_Associate/jid-1062.aspx
To apply for this job, visit: http://www.cslrecruitment.com/jobseekers/apply/?jid=1062
Or email your CV directly to me, Michela Nardini, at: michela@cslrecruitment.com
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