Clinical Research Associate

Equilab International; Indonesia; On-site; IDR 100,440,000 - 167,400,000; Full time

Job summary

Equilab International in Indonesia is seeking a Clinical Research Associate to ensure GCP-compliant trial quality, manage study documentation, and support site activities from start-up to close-out.

You will prepare protocol and CRFs, assist Ethics Committee submissions, handle regulatory filings, perform site feasibility and monitoring, and act as the liaison between investigators and sponsors. Travel flexibility is required, and you should communicate clearly with diverse teams.

Qualifications

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

Responsibilities

• 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

Skills

Good communication

Project management

Negotiation skills

English proficiency

Willing to travel

Education

Bachelor degree (Pharmacy or Science)

Job description

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.

Responsibilities

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

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

Required Skills

• Having Good Communication
• Project Management and Negotiation Skills