临床试验助理 CTA_Beijing

This is a CPA/CTA role in a TOP global pharma base******** Beijing.

Responsibilities an******** ******** but are not limite******** thefollowing:
1. Responsible for study documents f******** tracking an********an******** these activities performe******** compliance with GCP/SOPsan******** regulation.
2. Responsible for study administrative supports in compliance withaccording company policy an******** regulation.
3. Providing general administrative supports to CRAs an******** manager.
4. Establish an******** soun******** relationships with external(suppl******** agency) an******** customers (f******** IT) to providerequire******** to clinical trials.
5. This role shoul******** company's compliance an******** pol********an******** manage the daily activity to align with these accordingly.

Requiremen********
1. Diploma or Bachelor Degree or above. Overseas experience is a plus.
2. Majore******** Medical/pharmacological/Nursing/Science.
3. Understan******** or has GCP certificate.
4. 1.5-2 years working as a******** previous CTA/CPA/CTC/CRC experienceis preferred.
5. Clinical Research experience on multinational pharma or CROs is aplus.
6. Fluent English in rea******** writing an********.
7. Goo******** sk******** teamwork sp******** able to learn an********to IT system an******** equipment.
8. High motivation for the position an******** clear picture of whatthis position will do.