Essential Functions:

• TMF: Set up and maintain the site level TMF/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 ICF 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

Job Requirements:

• Bachelors Degree in Pharmaceutical or related field

• Min. 1 - 2 years of clinical trial experience in the pharmaceutical or CRO industry.

• Basic knowledge of applicable clinical research regulatory requirements; i.e., Good Clinical Practice (GCP) and International Conference on Harmonization (ICH) guidelines

• Broad knowledge of applicable protocol requirements as provided in company training

• Computer skills including working knowledge of Microsoft Word, Excel and PowerPoint

• Good written and verbal communication skills including good command of English language

IQVIA is a leading global provider of clinical research services, commercial insights and healthcare intelligence to the life sciences and healthcare industries. We create intelligent connections to accelerate the development and commercialization of innovative medical treatments to help improve patient outcomes and population health worldwide. Learn more at https://jobs.iqvia.com