Certified CRA along with master degree in Clinical pharmacology with more than a decade of hands on experience working in health related institutions and industry, proficient in QA/QC, & documentation, with knowledge of GMP, ICH & GCP guidelines and exceptional technical skills. A self-starter, with the ability to achieve results and balance multiple work assignments under minimum supervision. Clinical Trial Conduct & Monitoring Data collection/Data Management, Query Resolution • Enthusiastic, hardworking and meticulous• Excellent sense of planning and organization • Excellent ability to manage various responsibilities simultaneously and under pressure