Senior Clinical Trial Associate (FSP)
BEIJING, China 求人ID R0000034309 Category Clinical TrialsAbout this Role
Key Accountabilities:
Study Team Supporting
TMF: Set up and maintain the site level TF/eTMF, coordinate on document collection, uploading into SharePoint (SP)/eTMF, check the document completeness, and provide TMF/eTMF quality control (QC) if required.
EC Submission: Coordinate on EC submission dossier, site start-up preparation, and EC fee application and tracking.
Process protocol amendments; may include IF updates.
Tracker/Metrics Report: Collect and update study trackers/metrics report for site level if needed.
Site Contract and Payment: Assist in contract signature process; assist in site level payment initiative and payment and invoice tracking.
Site Materials and Equipment: Distribute site materials and equipment, document printing, shipment, and other administrative work.
Administrative: Business and department office administration support if required.
To undertake other reasonably related duties as may be assigned from time to time, as appropriate for level of experience.
Compliance with Parexel standards
Comply withrequired training curriculum.
Complete timesheets accurately as required.
Submit expense reports as required.
Update CV as required.
Maintain a working knowledge of and comply with Parexel processes, ICH-GCPs and other applicable requirements
Skills:
- Proven organizational and presentation skills.
Ability to manage multiple tasks and meticulous attention to detail.
Agile & quick learner, good team player
Willingness and ability to train others on study administration procedures.
Excellent written and verbal communication skills.
Good written and spoken English.
Computer Proficiency: ability to handle daily work via Microsoft Word, Excel, PowerPoint, and Outlook, etc.
Knowledge and Experience:
0.5 years of clinical trial experience in the pharmaceutical of CRO industry. Exceptions may be considered based on level of training and mentoring available.
Read, write, and speak fluent English; fluent in host country language may be required.
Excellent organizational skills and ability to prioritize and multitask.
2 or more years of clinical trial experience in the pharmaceutical or CRO industry.
Education:
Bachelor's degree or above in life sciences, English, and management.
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