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Vacancy details
Vacancy description:
Job Code:
MILANCTA
Job Title:
Clinical Trial Assistant - MILAN
Job Category:
Clinical Research
Contract:
Permanent
Discipline:
Clinical Trial Administrator
Country:
Italy
Location:
Any Location
Min experience:
1 years
Annual salary:
Negotiable
Apply by:
31 Jan 2009
**CANDIDATES ELIGIBLE TO WORK IN ITALY ONLY PLEASE** ICON is a global provider of outsourced development services to the pharmaceutical, biotechnology and medical device industries. We specialise in the strategic development, management and analysis of programs that support clinical development. ICON currently has over 4000 employees, operating from 52 locations in 30 countries. As part of our continuing expansion programme and organic growth we invite suitably qualified and experienced candidates for the following position in our MILAN offices.
• To assist the clinical research teams in ensuring the most effective and efficient conduct of clinical research studies by providing administration and project tracking support.
2. JOB FUNCTIONS/RESPONSIBILITIES:
• To support the clinical research teams with ongoing conduct of studies.
• To assist project teams with study specific documentation as appropriate;
- preparing study-specific procedures
- drug accountability records
- completion of status reports
- study newsletters and merge letters, etc.
• To become familiar with ICH GCP, appropriate regulations and relevant ICON SOP’s.
• To become familiar with the roles of the Clinical Research Associate (CRA) including site visits, if appropriate.
• To assist in the preparation, handling and tracking of Ethics/Regulatory submissions.
• To process Case Record Forms i.e. log in, tracking, quality control as appropriate for the study.
• To assist in co-ordination of Investigator payments.
• To maintain the study files for the project.
• To co-ordinate ordering/dispatch and tracking of trial materials e.g. CRFs, diary cards, lab supplies, drug supplies as appropriate.
• To assist project teams with trial progress tracking by updating the Clinical Trial Management systems.
• To be familiar with ICON internal tracking systems, as required.
• To assist in the tracking and distribution of safety reports.
• To organise project team meetings and investigator meetings and take minutes, as required.
• To co-ordinate document translation.
• To assist in the preparation of presentations.
3. QUALIFICATIONS/EXPERIENCE REQUIRED:
• Relevant work experience.
• Demonstrated organizational skills
• Computer literacy eg MS Word, Excel and Powerpoint.
• Good communication skills.
ICON is an equal opportunities employer and offers all employees competitive salary and benefits.
You must be logged in to apply for this position. Log in using the form on the right, at the top of the page beneath the logo, or click here to register.
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