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Vacancy details
Vacancy description:
Job Code:
J476724
Job Title:
Clinical Trial Administrator CTA
Job Category:
Clinical Research
Contract:
Locum/Temporary
Discipline:
Clinical Study Coordinator, Clinical Trial Administrator
Country:
United Kingdom
Location:
London - Central, Oxfordshire, London - North, London - East
Min experience:
N/A
Annual salary:
Negotiable
Apply by:
16 May 2008
We are looking for a flexible, pro-active CTA to work within our Global Clinical Operations team based at our High Wycombe site. We would like the ideal candidate to have at least 18 months CTA experience across a range of therapeutic areas (if possible). We would like the candidates to be familiar with GCP and we will provide training on our company SOPs and in-house systems.
Clinical Trials Assistant
Job Description
• Provide trial-related support to one or more Site Managers and Local Trial Managers working on J&J PRD Phase 1-3 global clinical trials programmes
• Perform all duties and activities according to the current list of Roles and Responsibilities
• Prepare and maintain accurate, up to date in-house trial-related files according to Company SOPs and local regulatory requirements
• Know and adhere to Company SOPs, ICH GCP and national regulatory requirements and local productivity targets
• Office-based, reporting to functional manager
• Assist in training of Company staff as required
Job Requirements
• Education - Secretarial or administrative qualification with at least two years experience of working in a medical, para-medical or pharmaceutical environment
• Clinical Drug Development – basic knowledge of clinical drug development and regulatory processes and procedures within J&J PRD Clinical Trials
• Teamworking – proactive contribution to and support of local Clinical Trial team activities
• Computer literacy – advanced keyboard skills and detailed knowledge of a variety of software packages (e.g. Excel, PowerPoint, Word). Use a range of computer based systems (e.g. Beacon, CTMS, ERPM) to track and monitor trial and investigational site-related activities
• Managing workloads – ability to organise multiple priorities and projects and work independently within area of responsibility
• Interpersonal skills - good command of spoken and written English, pleasant and positive telephone manner, ability to communicate effectively with investigational site staff, team members and functional manager
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