Swapna Dodla
St. Catharines,ON
Summary
Skilled clinical research coordinator with background in managing and overseeing clinical trials. Experience includes coordinating with research teams, ensuring compliance with protocols, and managing participant recruitment and data collection processes. Possess strong organizational skills, ability to manage multiple tasks efficiently, and capability to ensure accuracy in documentation and reporting. Contributed to improving trial procedures and enhancing data integrity in previous roles.
Overview
10
10
years of professional experience
Work History
Remote Intership
ICRA
MONTREAL, Quebec
12.2024 - Current
Clinical Research Coordinator
SMART (SUNSHINE MEDICAL ACADEMY FOR RESEARCH AND TRAINING)
Secunderabad, INDIA
08.2022 - 07.2024
- Coordinated investigator meetings, conference calls, and site initiation visits as needed.
- Collaborated with sponsors and investigators to carry out efficient and fully compliant research trials.
- Conducted routine visits to research sites to ensure compliance with protocol requirements.
- Performed patient assessments, collected and analyzed data, and prepared reports.
- Reviewed medical records for accuracy of source documentation prior to database lock.
- Monitored patient safety during clinical trials according to established guidelines.
- Gathered and reviewed study data.
- Developed case report forms for data collection at investigational sites.
- Organized investigator meetings; developed meeting agendas; created presentations; tracked action items from meetings; coordinated follow-up communications after meetings.
- Provided guidance on Good Clinical Practice regulations and other applicable regulatory standards.
- Reviewed CRFs for completeness and accuracy before database entry.
- Prioritized and organized tasks to efficiently accomplish service goals.
PHARM.D INTERN
APOLLO HOSPITAL
JUBILEE HILLS, INDIA
10.2014 - 09.2015
- Worked as a clinical pharmacist in cardiology, gynecology, endocrinology, orthopedics, psychiatry, and infectious diseases departments.
- Experienced and skilled in clinical pharmacy services, such as prescription audits, drug indenting, drug interactions, patient counseling, and IV admixtures.
- Assess patient information and prescriptions to identify drug treatment needs.
- Address therapeutic endpoints and outcomes for individual patients.
- Worked with pharmacy technicians to expedite urgent requests.
- Detected and reported therapeutic incompatibilities.
- Investigated discrepancies between verbal and written orders and actual product dispensed.
- Answered patient questions and data requests.
- Advised patients on potential drug interactions and side effects, proper dose timing and medication storage.
- Analyzed clinical data associated with medication orders received from providers.
- Delivered pharmacological education to patients by responding to and answering questions and explaining medication side effects.
- Conducted medication reviews to identify potential problems or adverse reactions with drugs prescribed.
- Reviewed prescription orders for completeness, accuracy, appropriateness of therapy, drug interactions, allergies.
- Supported timely and proper processing of prescriptions in collaboration with healthcare professionals.
- Collaborated with physicians and other healthcare professionals to ensure optimal patient care outcomes.
- Assessed patient needs based on medical history review prior to providing recommendations or advice on medication usage.
- Coordinated with pharmacists regarding changes in drug therapies or dosages due to new information or research findings.
- Participated in quality improvement projects to enhance pharmacy services and patient care.
- Participated in professional development activities such as attending conferences and seminars related to pharmacy practice.
- Checked medications for content, accuracy and completeness of drug packaging and labeling.
- Conducted comprehensive research and data analysis to support strategic planning and informed decision-making.
Education
Master of Science - Pharmaceutical Sciences
Sri Venkateshwara College of Pharmacy
India12-2015
Skills
- Case report management
- Research experience
- Documentation requirements
- Adverse event tracking
- Database organization
- Informed consent process
- Good clinical practice
- Clinical research ethics
- Research sops understanding
- Data analysis
- Study monitoring
- Clinical trial management
- Patient recruitment
- Study protocols
Languages
English
Native/ Bilingual
Hindi
Native/ Bilingual
Telugu
Native/ Bilingual
References
References available upon request.
Timeline
Remote Intership
ICRA
12.2024 - Current
Clinical Research Coordinator
SMART (SUNSHINE MEDICAL ACADEMY FOR RESEARCH AND TRAINING)
08.2022 - 07.2024
PHARM.D INTERN
APOLLO HOSPITAL
10.2014 - 09.2015
Master of Science - Pharmaceutical Sciences
Sri Venkateshwara College of Pharmacy
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