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Clinical Research QC Team Supervisor with a proven track record at Alliance Clinical Network, showcasing expertise in regulatory compliance (GCP, ICH Guidelines) and team leadership. Excelled in enhancing data quality assurance and streamlining processes, achieving a significant improvement in project timelines. Skilled in cross-functional collaboration and strategic planning, adept in Microsoft Office Suite. Seasoned Product Trainer with background in developing and delivering comprehensive product training programs. Strengths lie in ability to create engaging content, facilitate interactive sessions, and provide ongoing coaching for continuous improvement. Previously improved product understanding among teams leading to increased customer satisfaction and sales growth.

Highly skilled clinical research professional with a strong track record in coordinating and managing oncology clinical research studies. Proven ability to successfully oversee multiple trials from start to finish, ensuring strict adherence to regulatory guidelines. Exceptional communication skills, enabling effective collaboration with cross-functional teams.

Detail oriented professional experienced in clinical research with extensive experience in managing clinical trials, site monitoring, ensuring adherence to protocols, maintaining regulatory compliance and managing clinical trials from initiation to close out. Excellent organization and time management skills with demonstrated metrics and exceptional KPI's. Demonstrates methodical and results-driven approach to ensure high-quality data collection and reporting, resulting in successful project outcomes.

Senior Clinical Research Associate with 10+ years of independent monitoring experience across pharmaceutical, CRO, and academic research environments. Deep expertise in Phase I–IV trials, including early-phase, high-complexity, and safety-intensive studies. Extensive therapeutic exposure in immuno-oncology, ophthalmology, dermatology, CNS, cardiovascular, respiratory, infectious diseases, metabolic disorders, and rare diseases. Known for inspection-ready documentation, strong site relationship management, and the ability to resolve complex operational issues. Highly proficient in ICH GCP, risk-based monitoring, early-phase oversight, and cross-functional collaboration. Adept in EDC, CTMS, eTMF, and clinical quality systems with a consistent record of supporting high-enrolling, high-performing sites.
Knowledgeable Clinical Research Associate with several years of experience in documenting and assisting in clinical trials research. Clear, concise and effective written communication abilities. Thorough knowledge of FDA and GCP principles and regulations. Committed to providing support to the project team and executing responsibilities as instructed.
Motivated and methodical clinical research professional arranging sites, operations and regulatory functions. Proficient in data capture procedures and action planning. Seeking a dynamic, growth-oriented position.
Original Clinical Research Associate with exceptional analytical and communication skills. Profound knowledge of FDA regulatory requirements. Superior organizational, record retention and time management skills. Talented at designing clinical research projects and project plans.
Demonstrated skills in conducting clinical site visits and resolving issues related to participant eligibility, database protocols, or study procedures. Experience includes various types of clinical trials and studies.
Dedicated senior clinical research associate successful at evaluating sites, initiating trials and managing closeouts. Experienced with trials and successful at adapting to new processes. Bringing excellent organizational, planning and interpersonal skills gained during several-year career.

Supriya Chandranbavani

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Research Analyst

Associate Analyst

Intern

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B.Tech - Biotechnology

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Research Analyst

Associate Analyst

Intern

B.Tech - Biotechnology

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