 12+ years of overall experience.
 9+ years of experience in pharmacovigilance and drug safety.
 8+ years of experience in clinical Research.
 Proficiency in ARISg, Opticon, RAVE, Oracle Clinical data bases.
 Actively involved in all phases of Clinical Trials
 Easily adaptable to newer tools and technologies
 Having experience in clinical data analysis: analyzing clinical trial data, Narrative writing, SAE processing.
 Export the SAE report packets into a sponsor by using CIOMS, Med Watch, Appendix.11 format as desired by client
 Excellent understanding of SAE form, CRF, Lab report, MedDRA and ECG report
 Have Generated Reports using Data base.
 Flexible to changing prioriti...