Graduate CRA, Shanghai
About the role
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- Identifying investigators.
- Help, when requested, in preparation of regulatory submissions.
- Design patient information sheets and consent forms.
- Coordinate documents translation, verification and back translations where required.
- Ensure timely submission of protocol/consent documents/safety reports for Ethics/IRB approval according to local requirements.
- Pre-study/placement and initiation visits.
- Conduct regular monitoring visits in accordance with the ICON site monitoring SOP/Sponsor site monitoring SOP/WP, as appropriate
- Maintain all files and documentation pertaining to studies.
- Motivate investigators in order to achieve recruitment targets.
- Complete accurate study status reports.
- Deal with sponsor generated queries in a timely manner.
- Ensure the satisfactory close-out of investigator sites.
- Ensure correct archiving of files on completion of a study.
- Co-operate with sponsor and/or ICON QA personnel in the conduct of QA audits.
- Participate in feasibility studies for new proposals, as required
Requirements
- Ability to review and evaluate clinical data.
- Computer literacy
- Good oral and written communication skills.
- Bachelors degree, or local equivalent, in medicine, science or related discipline.
Impactful work. Meaningful careers. Quality rewards.
At ICON, our employees are our greatest strength. That’s why we are committed to empowering you to live your best life, both inside and outside of work. Whether your ambition is lead a global team, become a deep scientific or technical expert, work in-house with our customers or gain experience in a variety of different ICON functions, we will support you in realising your full potential. See all locations Learn more about Our Culture at ICON
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