Clinical research professional with expertise in regulatory compliance, patient recruitment, and accurate study documentation. Coordinates clinical trials and manages patient data to support study timelines and quality standards.
Overview
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Language
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Certification
Work History
Clinical Research Coordinator
Victoria hosiptal Bengaluru
Bengaluru, India
06.2025 - 08.2025
Coordinated clinical trials by overseeing patient recruitment, screening, and enrolment, ensuring streamlined research operations.
Monitored patient health and safety during trials, promptly addressing adverse events to ensure participant well-being.
Managed patient follow-up to enhance engagement and adherence to study protocols, contributing to overall trial integrity.
Scheduled and conducted follow-up visits with participants, ensuring continued engagement and protocol adherence.
Collected, processed, and analysed biological samples as per study protocols, contributing to research findings.
Organised and maintained patient records and research data under confidentiality rules.
Liaised with project teams to establish timelines and systems to monitor recruitment and protocol compliance.
Designed and implemented clinical research protocols to meet study objectives, adhering to ethical standards.
Assisted in the development and revision of research study materials, including patient information sheets and consent forms.
Coordinated logistics for clinical trial supplies, including storage, inventory, and distribution to trial sites.
Developed training materials and delivered sessions for research staff, ensuring high standards of practice.
Monitored use of supplies, equipment and services to identify and correct overspend.
Supported the study coordinator in day-to-day clinical study management across all participating sites.
Education
MSc - BIOTECHNOLOGY
Bangalore University
Bengaluru
12-2023
BSc - BIOTECHNOLOGY
Bangalore Citi University
Bengaluru
10-2021
Skills
Clinical trial management
Clinical data management
Patient recruitment and scheduling
Informed consent process
Adverse event monitoring
Safety reporting and compliance
Regulatory compliance awareness
Pharmacovigilance expertise
ICH-GCP guidelines knowledge
Good clinical practice (GCP)
Protocol development and case report form (CRF) expertise
Data analysis and statistical evaluation
Electronic trial master file (eTMF) management
Laboratory stock control and sample processing
Record keeping and accountability in compliance monitoring
Multitasking efficiency
Verbal and written communication skills
Patient advocacy and communication
Statistical analysis
Electronic trial master file (eTMF)
Sample processing
Laboratory stock control
Record keeping
Accountability in compliance monitoring
Multitasking efficiency
Multitasking efficiency
Verbal and written communication
Patient communication
Critical analysis
Microsoft Office proficiency
Clinical trial regulations
Patient advocacy
Critical analysis
Protocol development
Microsoft Office proficiency
Clinical trial regulations
Patient advocacy
Additional Information
Languages: English, Kannada, Telugu.
Certification
NIDA Clinical Trials Network Certificate of Completion. Completed Advance DiplomaClinical Research course by CLRI,in Bengaluru. Completed Poornayu ResearchLabs in Analytical
SAS Program from Linkedin
Analytical Instruments by Dr. Arun Kumar. S, in Bengaluru
Websites, Portfolios, Profiles
https://www.linkedin.com/in/sreelekhasr
PROJECT
Extraction and Characterization of Bioactive Secondary Metabolites from Fusarium fujikuroi for Antimicrobial Activity Evaluation
Conducted microbiological research and laboratory experiments Recorded, analyzed and interpreted experimental observations Prepared scientific reports and maintained
laboratory documentation Developed analytical, documentation and data interpretation skills
Clinical Research Coordinator at UCI Chao Family Comprehensive Cancer CenterClinical Research Coordinator at UCI Chao Family Comprehensive Cancer Center
Clinical Research Coordinator at Centre Hospitalier de l’Université de Montréal (CHUM)Clinical Research Coordinator at Centre Hospitalier de l’Université de Montréal (CHUM)