Clinical Research Associate position with a biotechnology firm focusing on clinical research and pharmaceutical products development. Highlights of Qualifications: In-depth knowledge of Clinical Research including ICH GCP guidelines, Clinical Trial Monitoring and Research Site Coordination Excellent skills in communication (both oral and written), collaboration and software applications and flent in English language Result-oriented and decisive Relevant Skills : Study Planning Activities, Identify potential investigators, Design CRFs and send draft CRFs for review; Plan Investigator meeting; Collect and submit regulatory-/company-required documents; IRB approval(s); Conduct site initiation visits; Monitor site visits reports for any required action; Assure all adverse events are reported according to regulations and company policy; Review protocol compliance, focusing on inclusion/exclusion requirements; Assure required corrections are made; Review drug accounting, storage, dispensing; Check for new adverse events; Prepare final study reports; Ensure study file is complete and ready for audit.