Clinical Research Associate

Responsible for clinical trial preparation, clinical trial implementation quality control, and clinical site closure. A Clinical Research Associate is responsible to ensure that results and data are of high quality standard in accordance with GCP requirements.

Job Description :

• Prepare clinical study documents (protocol, CRF, informed consent form, etc.)
• Assist Principal Investigator for Ethics Committee submission
• Responsible for Regulatory Affairs submission
• Perform site feasibility, investigator selection, and site set up
• Perform clinical trial monitoring, follow up and discussion with study site team
• Responsible for maintaining trial documentation
• Acting as a communication line between investigator and sponsor

Qualifications:

• Bachelor Degree from Pharmacy or Science
• At least 1 year experience as the CRA, Regulatory/Registration in Pharmaceutical Companies, Clinical Research Industry or Hospital
• Independent, detail and high compliance
• Having good communication and negotiation skills
• English proficiency is preferably
• Open & flexible to travel