Microsoft Office
Rishi Rawal
Analyst
New Delhi
Summary
Data Analyst with 3+ years of experience in healthcare research and analytics. Proven ability to collect, clean, analyze, and interpret large datasets to identify trends, patterns, and insights. Expertise in using statistical software and data visualization tools to communicate findings to stakeholders.
- Developed and implemented a data-driven approach to improve clinical trial recruitment and retention rates.
- Led a team of analysts in the development of a predictive model to identify patients at risk for adverse events.
- Presented findings to senior management and stakeholders to inform decision-making.
Overview
5
5
years of professional experience
8
8
years of post-secondary education
3
3
Languages
Work History
Analyst
CI Scientists
Bengaluru, Karnataka
02.2024 - Current
- Covered AACR & ASH conference
- Dedicatedly working on Neuroscience & Oncology portfolio with hands on exposure in (MDD, Schizophrenia, Bipolar disorder, Generalized Anxiety disorder & Solid tumors)
- Worked on generating Daily newsletter, Quarterly/monthly reports, Clinical Trial attributes, Competitive Landscapes, Company profiles, Product profiles, CI insights and recommendations
- Monitoring and analysis of Commercials, Regulatory updates, Clinical activities, Conference results, Annual Reports and Investor presentation & Interpreting complex data to generate meaningful insights
- Enhanced team collaboration by providing clear communication of complex findings through visualizations and reports.
- Increased efficiency by streamlining data analysis processes and implementing automation tools.
Analyst
STEM Healthcare (INIZIO Advisory)
Gurgaon
02.2023 - 10.2023
- Handled 14 Projects by:
- Creating various Excel documents to assist with pulling metrics data and presenting information to stakeholders for concise explanations of best placement for needed resources.
- Producing monthly reports using advanced Excel spreadsheet functions.
- Extracting and interpreting data patterns to translate findings into actionable outcomes.
- Developing required policies and procedures that reflected actual goals, tasks and workflows, while meeting all regulatory compliance requirements.
- Documenting effective and replicable methods for extracting data and organizing data sources.
Freelance Clinical Research Associate
Drugs For Neglected Disease Initiative | Shodh Clinical
New Delhi
03.2022 - 01.2023
- Handled Drug repurposing (phase III) clinical Trials (Adaptive Platform) on COVID & MDR-TB.
- Conducted clinical trial in accordance with protocol and recorded and monitored progress.
- Collaborated with clinical study site and sponsor to troubleshoot and provide solutions to study-related issues.
- Coordinated and scheduled protocol-related visits and required testing to demonstrate vigilance in patient safety, protocol compliance and data quality.
- Maintained site monitoring schedules to facilitate effective communication with members of clinical team.
- Facilitated quality of clinical trials by establishing project schedules and monitoring support to encourage accuracy and efficiency.
- Monitored safety of human subjects and oversaw consent procedures to comply with local and National regulations.
- Oversaw project developments to provide quality deliverables while maintaining optimal efficiency.
- Gathered and organized clinical trial documentation to meet rigorous standards for site approval.
- Assisted in investigator selection and qualification process to provide capable investigators with adequate resources to properly conduct trials.
- Reviewed participant eligibility and consent documentation to help researchers achieve accurate and meaningful results.
- Interfaced with clinical investigators and site staff to foster ethical research consistent with research plans.
- Liaised with ICMR, HMSC department for project development.
- Traveled to investigative sites to conduct site qualification, initiation, interim monitoring and close-out visits to maintain and enforce regulatory compliance.
- Submitted routine Site feasibility, Site Initiation & Monitoring reports and follow-up letters to facilitate internal and external communication.
- Reviewed data queries and listings and worked with study centers to resolve data discrepancies.
- Created and maintained database and records filing system to document data on specimen collection, processing and storage.
- Reviewed clinical data, source documentation, case report forms and investigative site regulatory files to verify accuracy and completion.
- Checked compliance with drug storage procedures to comply with protocols and SOP requirements.
- Conducted meetings with sponsor representatives to discuss clinical study developments.
- Liaised with clinical investigator to identify, assess and resolve site performance, quality and compliance issues.
- Liaised with clinical project leader to effectively resolve study-related issues.
- Implemented electronic data capturing systems to adhere with clinical research guidelines.
- Leveraged knowledge of excel, expertise and problem-solving techniques to resolve investigative site issues.
Lead Research Officer
ESIC Medical College and Hospital, COVID Vaccine
Faridabad
07.2021 - 03.2022
- Handled Vaccine trial (Phase III), Drug Repurposing (Phase III), Pediatric (Observational Study)
- Conducted research, gathered information from multiple sources and presented results.
- Coordinated with advanced practitioners and physicians during pre-study visits, staff orientation, study startup to close out, drug accountability, patient screening, enrollment and follow up, study reimbursement and data collection, sustaining GCP requirements at all times.
- Organized and facilitated investigator and coordinator meetings, conferences and events associated with research activities.
- Established connections with liaisons to industrial and commercial stakeholders, allowing industry trends to inform research and vice versa.
- Developed team communications and information for meetings.
- Actively listened to Patient requests, confirming full understanding before addressing concerns.
- Used critical thinking to break down problems, evaluate solutions and make decisions.
- Improved operations through consistent hard work and dedication.
- Created spreadsheets using Microsoft Excel for daily, weekly and monthly reporting.
- Collaborated with team members to achieve target results.
Clinical Trial Assistant
IQVIA
New Delhi
09.2020 - 07.2021
- Handled device trial (neurology domain) (Phase III), Vaccine trial (Phase III) , Drug Trial (diabetes and oncology indication) (Phase IV).
- To manage various projects including Device trial (neurology domain), Vaccine trial, Drug Trial (diabetes and oncology indication)
- Collaborated with medical and administrative personnel to maintain patient-focused, engaging and compassionate environment.
- Collaborated with clinical study site and sponsor to troubleshoot and provide solutions to study-related issues.
- Coordinated and scheduled protocol-related visits and required testing to demonstrate vigilance in patient safety, protocol compliance and data quality.
- Maintained site monitoring schedules to facilitate effective communication with members of clinical team.
- Facilitated quality of clinical trials by establishing project schedules and monitoring support to encourage accuracy and efficiency.
- Monitored safety of human subjects and oversaw consent procedures to comply with local and National regulations.
- Reviewed data queries and listings and worked with study centers to resolve data discrepancies.
- Created and maintained database and records filing system to document data on specimen collection, processing and storage.
- Conducted initiation, monitoring and closeout visits to verify study procedures, regulatory documents and data completion.
- Mentored team New CTAs by sharing suggestions and encouraging ideas to deliver successful studies.
Clinical Research Coordinator
Cytespace
New Delhi
06.2020 - 09.2020
- Handled 2 Hospitals in DDRD | CSIR | DRDO | Sponsored- Phase III (Device Trial)
- Screened patient records, databases and physician referrals to identify prospective candidates for research studies.
- Collected data and followed research protocols, operations manuals and case report form requirements.
- Followed informed consent processes and maintained records.
- Gathered, processed and shipped lab specimens.
- Collected, evaluated and modeled collected data.
- Maintained compliance with protocols covering patient care and clinical trial operations.
- Participated in initiation visits and investigator meetings, implementing trials in accordance with study timelines and budgets.
- Worked with principal investigator and sponsors to facilitate daily trial activities and comply with research protocols.
- Learned new skills and applied to daily tasks to improve efficiency and productivity.
- Resolved problems, improved operations and provided exceptional service.
- Worked flexible hours across night, weekend and holiday shifts.
- Led projects and analyzed data to identify opportunities for improvement.
- Used coordination and planning skills to achieve results according to schedule.
- Created spreadsheets using Microsoft Excel for daily, weekly and monthly reporting.
Education
Master of Science - Pharmacology
Jamia Hamdard University
New Delhi, India 07.2018 - 07.2020
Bachelor of Science - B.Pharmacy
Lovely Professional University
New Delhi, India 06.2014 - 06.2018
XII - PCB
S.C.D. Govt. College
Punjab, India 06.2013 - 06.2014
Xth -
Sacred Heart Convent School
Punjab, India 06.2011 - 06.2012
Skills
Technical skills
undefinedAccomplishments
- ICH GCP E6(R2) Trained And Certified, The global health network (2020)
- Qualified GPAT 4 Times (2015,2017-19)
- N.C.C “B-Certificate” Holder from 3-PUNJAB Battalion (2012)
- Attended Safety Reporting Workshop, By Shodh Clinicals
- ICH GCP E6 (R2) Training & Certification, By SWISS TPH, Geneva(2022)
Workshops & Conferences
Software
Power Automate
Clini-ops, Nuckleus, Veeva Vault, Wingspan, Infolink-2, Open-Bots, MS Office, DD solver, Endnote, Mendeley, Adobe Photoshop
Timeline
Analyst
CI Scientists
02.2024 - Current
Analyst
STEM Healthcare (INIZIO Advisory)
02.2023 - 10.2023
Freelance Clinical Research Associate
Drugs For Neglected Disease Initiative | Shodh Clinical
03.2022 - 01.2023
Lead Research Officer
ESIC Medical College and Hospital, COVID Vaccine
07.2021 - 03.2022
Clinical Trial Assistant
IQVIA
09.2020 - 07.2021
Clinical Research Coordinator
Cytespace
06.2020 - 09.2020
Master of Science - Pharmacology
Jamia Hamdard University
07.2018 - 07.2020
Bachelor of Science - B.Pharmacy
Lovely Professional University
06.2014 - 06.2018
XII - PCB
S.C.D. Govt. College
06.2013 - 06.2014
Xth -
Sacred Heart Convent School
06.2011 - 06.2012
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