Dancing
Sreyasee Banerjee
Senior Research Associate III
Bengaluru,KA
Summary
Dynamic Senior Research Associate III with a proven track record at Advarra, enhancing productivity through innovative data management tools. Expert in clinical trial management and budgeting, I excel in cross-functional teamwork and critical thinking, ensuring compliance and patient safety while mentoring junior researchers to achieve project success. Also, specializes in establishing project objectives, developing experimental plan and effectively prioritizing tasks to meet time sensitive delivery goals. Serves as point person for executing clinical research projects and disseminating findings to leadership. Displays strong written and oral communication skills to present complex analyses effectively.
Overview
6
6
years of professional experience
9
9
Certifications
4
4
Languages
Work History
Senior Research Associate III
Advarra
04.2021 - Current
- Increased overall productivity by implementing new software tools for data management and analysis.
- Evaluated emerging technologies for potential integration into ongoing research efforts.
- Established productive relationships with external partners for collaboration on joint research initiatives.
- Developing clinical trial financial contracts and budget negotiations.
- Mentored junior researchers, contributing to their professional growth and development.
- Clinical Trial protocol interpretation and comprehension ensuring protocol compliance, data integrity and patient safety throughout trial process.
- Mentored team members by sharing suggestions and encouraging ideas to deliver successful studies.
- Conducting kick-off meetings and regular project meetings until the study goes live.
- Serving as the head for clinical projects for Yale University, Fox Chase Cancer Center, Oregon Health and Science University, Emory University, and Weill Cornell Medical College, to name a few.
- Expertise in CTMS, Zendesk, Longboat, OKTA, Outlook, Medidata, and RAVE.
- Conducted clinical trial in accordance with protocol and recorded and monitored progress.
- Coordinated and scheduled protocol-related visits and required testing to demonstrate vigilance in patient safety, protocol compliance and data quality.
- Collaborated with clinical study site and sponsor to troubleshoot and provide solutions to study-related issues.
- Gathered and organized clinical trial documentation to meet rigorous standards for site approval.
- Reviewed data queries and listings and worked with study centers to resolve data discrepancies.
- Conducted initiation, monitoring and closeout visits to verify study procedures, regulatory documents and data completion.
- Collaborated with cross-functional teams to successfully meet project timelines and deliverables.
- Liaised with clinical project leader to effectively resolve study-related issues.
- Interfaced with clinical investigators and site staff to foster ethical research consistent with research plans.
- Reviewed clinical data, source documentation, case report forms and investigative site regulatory files to verify accuracy and completion.
- Liaised with clinical investigator to identify, assess and resolve site performance, quality and compliance issues.
- Oversaw project developments to provide quality deliverables while maintaining optimal efficiency.
SME - Biology
Dimentics Pvt Ltd
08.2020 - 04.2021
- Enhanced the quality of subject matter content, resulting in an improvement in user engagement and satisfaction.
- Worked on the SME-Biology project to ensure high-quality results for biology-related content.
- Implemented comprehensive research and analysis for the best quality content.
Education
Master of Science - Biochemistry
REVA University
Bengaluru, India 04.2001 -
Bachelor of Science - Life Science- Biochemistry, Genetics And Biotech
Bangalore University (Garden City College)
Bengaluru 04.2001 -
Skills
Works Well Under Pressure
MS office
Critical thinking
Team collaboration
Budgeting and finance
Protocol development
Attention to detail
Effective multitasking
Cross-functional teamwork
CTMS
Clinical data management
Quality control
Study design
Case report forms
Electronic data capture
Action planning
Site monitoring
Patient safety
Clinical study reports
ICH guidelines
Clinical trial management
Informed consent process
Adverse event reporting
Good clinical practice
Accomplishments
- High Achiever Award from Advarra for outstanding performance multiple times.
- Excellence Award from Advarra
- Standing Ovation Award from Advarra.
- Customer Champion Award from Advarra.
- Consistently exceeded expectations and delivered exceptional results.
- Recognized for consistently going above and beyond in all projects and initiatives.
Certification
Clinical SAS Programming - UDEMY
Interests
Writing short stories/poems
Photography
Adventure bike riding
Timeline
Senior Research Associate III
Advarra
04.2021 - Current
SME - Biology
Dimentics Pvt Ltd
08.2020 - 04.2021
Master of Science - Biochemistry
REVA University
04.2001 -
Bachelor of Science - Life Science- Biochemistry, Genetics And Biotech
Bangalore University (Garden City College)
04.2001 -