Responsibilities:
Understand GCP and SOP of clinical research

Assist CRM/PM/ CRA to prepare and maintain study document

Review in-house documents, track and review Investigational Product and other materials

Assist to resolve all outstanding DCFs as applicable

Assist site payment and tracking

Actively implement quality control procedures. Maintain high quality standards, through accuracy and quality of work

Generate regular assigned reports and prepare presentation slides

Responsible for filing and archiving of clinical documents

Qualifications:
College degree. Pharmacology or biology preferred.

Good communication, coordination and organization skills

Good analytical and problem solving skill

Prefer to have good command of English in speaking, listening, reading and writing

Familiar with IT software e.g. Microsoft Word, Excel,