Clinical Trial Administrator-FSP
3 weeks ago
Clinical Study Support
At Parexel, we strive to achieve excellence in our clinical trials. As a Clinical Trial Administrator-FSP, you will play a crucial role in ensuring the successful and timely completion of all clinical trial milestones.
Your Responsibilities:
- Assist the CO team with in-house activities and documentation associated with the set up and management of trial activities.
- Coordinate translations of documents after review/translation and submit for TMF filing.
- Support the CRA to prepare the safety information submission per site-specific requirement.
- Create and update the ISF, including paper ISF and binders.
- Support study routine supplies purchase, distribution, calibration validity of loaned equipment.
- Assist in organization and execution of investigator meeting.
- Maintain study information in CTMS on behalf of the Clinical Trial Manager.
Central Administrative Support
As a Clinical Trial Administrator-FSP, you will also provide logistic support, organization to CO internal and external meetings, trainings.
Requirements:
- Bachelor's degree in a related field.
- Good organizational and communication skills.
- Well-understood Good Clinical Practice, ICH-GCP.
- Command of Microsoft Office applications.
- Ability to work as a team and backup team members.
- Minimum 1 year of working experience in the pharma industry or related industry.
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