Description
Professional Summary My experience of 10 years' in Health care Domain - 3 years. in Clinical Research and 7 yrs. in Clinical practice makes me an expertise in both Therapeutic & Research Industries A certified professional Clinical Research Coordinator with 3 years of experience in Clinical Research coordination. Demonstrated ability to support the management and coordinate the tasks of multiple clinical research studies. Expert in liaising between different departments. Special talent for creating and maintaining databases and reports. Areas of Expertise : * Project Planning * Pharmacovigilance * Clinical Monitoring * Direct communications with CRO & IEC * Designing recording & maintaining various clinical study documents like AE SAE CRF, ICF Source documentation, Study Protocol etc * Medical ICD 10 coding ( WHO guidelines) MEDRA * Phase II - IV Clinical trials * Device trials * Genetic study of neonates * Internal IEC/ IRB communications * Clinical Data Collection Skill Highlights: Curriculum Vitae * Research and Analysis * Pharmacovigilance * Safety Standards * Medical Coding - MEDRA, ICD- 10 * Data Compilation & Data QC Record Accuracy * Staff Training Team Collaboration * Critical Thinking Time Management * Written/Verbal Communication * Effective Multitasking * Extensive Organizational Skills * Strong clinical judgment * Extensive medical terminology knowledge * Microsoft Office Accomplishments * Compliance - Maintained compliance with regulatory standards * Patient Care - Delivered compassionate care that exceeded hospital requirements. Successfully provided quality care to patients coming for Clinical Trials in KEM Hospital research Center * Documentation - Ensured data accuracy through precise documentation * Gold medalist in Graduate College at all University level Examination * First in the subject of Clinical Medicine in Final year of Bachelor Examination. * Second in University Merit List in First year of Bachelor Examination * Played a key role in conducting Device trial research and experiments that concluded in FDA submission.
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