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Clinical Trial Assistant

Beijing
Permanent
Reference: JR065746
This vacancy has now expired.
Description

This is an exciting opportunity to join ICON.

ICON, a leading Clinical Research Organization, is seeking passionate, resilient and inspiring professional to join our team as a Clinical Trial Assistant. This opportunity offers an entry-level permanent position to highly skilled individuals interested in a career in clinical research based in Beijing, China.

This is an exciting opportunity to work within a fast paced, busy environment for a leading global provider of outsourced development services to the pharmaceutical, biotechnology and medical device industries. As a Clinical Trial Assistant (CTA) you have 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.



JOB FUNCTIONS/RESPONSIBILITIES:
* To provide general administrative support to the Clinical Operations Department

* To assist the Clinical Operations teams in completion of all required tasks to meet departmental and project goals.
* To support the Clinical Operations teams with ongoing conduct of studies.
* To be familiar with ICH GCP, appropriate regulations, relevant ICON SOP's and ICON internal tracking systems.
* To be familiar with the roles of the Clinical Research Associates (CRA)

* To assist project teams with study specific documentation and guidelines as appropriate.
* To set up, organize and maintain clinical study documentation including preparation for internal/external audits, final reconciliation and archival.
* To process Data Collection Forms i.e. log in, tracking, quality control as appropriate for the study.
* To assist in quality control audits of clinical study documentation

* To co-ordinate ordering/dispatch and tracking of trial as appropriate.
* To assist project teams with trial progress tracking by updating the Clinical Trial Management systems.
* To copy and route incoming correspondence, internal documentation, CRFs, etc., as appropriate.
* To assist in co-ordination of Investigator payments, if applicable.
* To contact clinical sites for specific requests

* To assist in the tracking and distribution of safety reports.
* To co-ordinate document translation, if required.
* To attend project team meetings and generate meeting minutes.
* To assist the Project Manager and project team with Investigator Meeting coordination, activities preparation and generate meeting minutes.
* To assist in the production of slides, overheads, etc., as needed for project, departmental, sponsor and/or business development presentations.
* To assist with the coordination of team member tracking.



QUALIFICATIONS/EXPERIENCE REQUIRED:

* Either relevant work experience or bachelor's degree holder

* Clinical research or health care related academic or work experience preferable.
* Good organizational skills, ability to manage multiple tasks and meticulous attention to detail.
* Good written and verbal communication skills.
* Good written and spoken English.
* Computer literacy: e.g. Microsoft Word, Excel, PowerPoint, Outlook.

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, including disability/veteran, and committed to providing a workplace free of discrimination and harassment.

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