Clinical Research Associate

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
- Bachelors degree from Pharmacy (preferably Apothecary graduates)
- 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 preferred
- Open & flexible to travel

Keuntungan
- Salary Package
- Health Insurance
- Working Culture & Career Growth

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