Piya Das
Clinical Research Coordinator @Respirology & Rheumatology Associates
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WORK HISTORY
Clinical Research Coordinator @Respirology & Rheumatology Associates
Windsor, ON, CA
1.Supported 25+ clinical trials in Respirology and 6+ in Rheumatology across Phases II, and IV, ensuring high standards of regulatory and protocol compliance.2.Led screening, enrollment, and monitoring of study participants, maintaining close follow-up and consistent subject engagement throughout the trial lifecycle.3.Performed direct patient care activities including assessments, study drug administration, ECGs, spirometry, and collection of biological samples with accuracy and care.4.Oversaw accurate and timely documentation, including case report forms (CRFs), source data, and adverse event (AE/SAE) reporting in alignment with GCP guidelines.5.Managed electronic data entry and tracking using EDC systems, ensuring completeness, accuracy, and data integrity.6.Facilitated IRB submissions and maintained regulatory documents to meet study timelines and institutional requirements.7.Conducted study initiation processes, eligibility reviews, and informed consent discussions per protocol criteria.8.Maintained organized study files, temperature logs, and investigational product accountability records.9.Liaised with sponsors and monitors, addressed site visit findings, and implemented PI-approved recommendations.10.Trained and mentored new research staff on study protocols, documentation standards, and regulatory best practices.
EDUCATION
University of Windsor
Master's degree, Biotechnology
University of Dhaka
Bachelor of Medicine, Bachelor of Surgery - MBBS, Medicine
ABOUT PIYA DAS
I am a passionate Clinical Research Professional with over 5 years of experience in patient management and clinical trial coordination. With a foundation in medicine and biotechnology, I bring a unique blend of scientific knowledge and hands-on medical practice to the field of clinical research.My experience includes working in hospital settings as a Clinical Research Coordinator, where I honed my skills in patient engagement and protocol adherence, and transitioning into client-focused roles within the CRO industry.I thrive in collaborative environments and am committed to supporting clinical trials that advance new therapies and improve patient outcomes. I am eager to expand my expertise in all facets of clinical research and contribute to innovative, patient-centered studies.Let’s connect if you’re looking to collaborate or share insights on advancing clinical research and improving healthcare through rigorous trials
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