Graduate CRA, Chengdu / Wuhan
About the role
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"At ICON, it's our People that set us Apart"
ICON plc is a global provider of drug development solutions and services to the pharmaceutical, biotechnology and medical device industries. The company specialises in the strategic development, management and analysis of programs that support clinical development - from compound selection to Phase I-IV clinical studies. With headquarters in Dublin, Ireland, ICON currently, operates from 83 locations in 38 countries and has approximately 12,600 employees. Further information is available atwww.iconplc.com
Graduate CRA
The Graduate CRA will be trained for the role of Clinical Research Associate within ICON. Clinical Research Associates identify, select, initiate and close-out appropriate investigational sites for clinical studies. They are responsible for monitoring those sites in order to ensure that studies are carried out according to the study protocol and in accordance with ICON SOPs/WPs, applicable regulations and the principles of ICH GCP. You will assisting with coordinating all the necessary activities required to set up and monitor a study, including the following:
- 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.
This is an excellent opportunity to receive structured and supportive formal training and on the job training to ensure that you are set up for success.
Benefits of Working in ICON
Other than working with a great team of smart and energetic people, we also offer a very competitive benefits package. This varies from country to country so a dedicated recruiter will discuss this with you at interview stage.
We care about our people as they are the key to our success. We provide an open and friendly work environment where we empower people and provide them with opportunities to develop their long term career.
ICON is an equal opportunity employer - M/F/D/V and committed to providing a workplace free of any discrimination or harassment.
At ICON, it's our People that set us Apart"
A better career. A better world. A better you.
Our people are our greatest strength, are the core of our culture and the driving force behind our success. Throughout all levels of the company, our people have a drive to succeed and a passion that ensures what we do, we do well. We help you build exciting and rewarding careers, deliver results to help bring life-changing medicine and devices to market and maintain ICON’s success as an industry leader. See all locations Read more
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