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Amulya Sampagadde

Clinical Research Coordinator at Red Maple Trials Inc

Based in Ottawa, Canada

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Seniority

Staff

Department

Healthcare & Human Services

Location

Ottawa

Industry

Research Services

Company size

13

Contact information

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Email

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a•••••••@redmapletrials.com

Phone

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Background

About Amulya Sampagadde

Highly qualified in medical research professional with more than 6 years of experience in research methodologies, protocols, regulatory requirements, database management and study coordination. Over the course of multiple research projects, I collaborated closely with the patient engagement manager, successfully establishing database query reviews for study candidacy and conducting outbound calls for interested patients. My responsibilities also included identifying suitable study candidates based on my knowledge of sites' recruiting and upcoming studies. Proficient in databases such as EDC, CTMS and ACCURO, I prioritize problem-solving and teamwork, with meticulous attention to detail and accuracy. As a research scholar in India for three years, I have a proven track record in designing research studies, meticulously crafting study protocols, and securing informed consent forms (ICFs). My commitment to detail extends to the management of case report forms (CRFs), ensuring accuracy and completeness in data collection. A key aspect of my role involved conducting data analysis using fundamental statistical techniques, providing actionable insights that enhanced decision-making processes. I actively contributed to the strategic planning of pilot studies under the guidance of the Qualified Investigator/Principal Investigator, offering vital information for assessing study feasibility, including considerations such as study costs, timeframes, resource allocation, data quality, and data capture efficiency. My proficiency in public presentation development was showcased through my role in creating engaging and persuasive presentations using various media and technologies. I successfully facilitated the presentation of study protocols to the Research Ethics Board (REB) for approval at Rajiv Gandhi University of Health Sciences (RGUHS). In addition to my strategic contributions, I monitored study progress and provided regular updates to the REB. My commitment to disseminating research findings is reflected in my preparation of manuscripts and successful publication in a peer-reviewed journal. With a collective experience of 2 years in Canada and 3 years in India, I possess a solid foundation of knowledge and skills in clinical research.

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