Jyoti D.
About Jyoti D.
Jyoti D. is a Clinical Trial Associate at Bristol-Myers Squibb in Mulgrave, Victoria, Australia, with extensive experience in clinical operations and research.
Current Professional Roles
Jyoti D. currently holds several positions at Syneos Health in Australia, including Clinical Trial Manager for Bristol-Myers Squibb, Senior Clinical Operations Specialist, and Clinical Operations Specialist. Additionally, she serves as a Clinical Trial Associate at Bristol-Myers Squibb in Mulgrave, Victoria.
Previous Professional Experience
Jyoti D. has a diverse range of prior work experience. She worked at Nucleus Network as a Clinical Unit Assistant from 2017 to 2019 in Melbourne. Before that, she was a Receptionist/Dental Assistant at Williamstown Road Dental Surgery from 2016 to 2017. She has also served as a Database Administrator at The Lost Dogs' Home in North Melbourne from 2013 to 2016 and as a Clinical Research Assistant at Evolvus in Pune from 2010 to 2013. Earlier in her career, she was Faculty / Administration Incharge at Suryadatta Group of Institute from 2008 to 2010 in Pune, India.
Educational Background
Jyoti D. has pursued extensive education in various fields. She achieved ARCS Australia – Professional Development in Therapeutics with a Clinical Trials Certification in 2017. In 2016, she completed a Certificate 3 in Pathology Collection and First Aid from All Health Training. She holds a Master of Science degree in Bioinformatics from Sikkim Manipal University - Distance Education, completed between 2005 and 2007. Jyoti also has a Bachelor's of Science degree in Botany/Plant Biology from Fergusson College, earned between 2003 and 2005.
Skills and Proficiencies
Jyoti D. is fluent in both English and Indian languages and is skilled in multiple operating systems, including Windows XP, Windows 7, and Windows 8. She is proficient in Microsoft Office Suite (Excel, Word, PowerPoint, Outlook) and adept at using custom database tools and software. Jyoti quickly learns and adapts to new systems, processes, and procedures, and she works well under pressure while maintaining a positive attitude. She possesses substantial knowledge of ICH-GCP Guidelines, CRF designing, protocol design, regulatory aspects, and clinical trials.