Supriya T

Location: Bengaluru

Summary

Aspiring Clinical Data Management professional currently pursuing certification, with hands-on exposure to Medidata Rave, Oracle Clinical, and CTMS tools. Seeking an entry-level CDM role to apply skills in CRF design, regulatory compliance, and data quality management.

Technical Skills

• Clinical Trial Protocol Interpretation
• Case Report Form (CRF) Design
• Medidata Rave, Oracle Clinical
• Electronic Data Capture (EDC) Systems
• Clinical Trial Management System (CTMS)
• ICH-GCP Guidelines
• Data Cleaning & Query Management
• Clinical Document Management (eTMF, Veeva Vault)

Soft Skills

• Attention to Detail
• Problem-Solving
• Communication & Teamwork
• Documentation & Reporting
• Time Management

Education

• Master of Science (Pursuing) – Reva University, Bengaluru (2023–2025) – CGPA: 8.0
• Bachelor of Science – Jyoti Nivas College (Autonomous), Bengaluru (2020–2023) – CGPA: 6.2

Certification

• Clinical Data Management Certification – Biotecnika (In Progress: March 2025 – July 2025)
• – Medidata Rave, Oracle Clinical
• – GCP & ICH Guidelines
• – CRF Design & Validation
• – Query Management
• – Data Cleaning
• – EDC Tools & Clinical Trial Processes

Experience

• Food and Water Analyst Intern – Fogiene Sciences (NABL Accredited)
• Jan 2025 – April 2025
• – Performed chemical and microbiological analysis of food and water samples
• – Maintained documentation according to NABL standards
• – Generated and reviewed reports using MS Excel
• – Gained experience in compliance and documentation accuracy

Projects

• Clinical Trial Document Management using Veeva Vault eTMF (Ongoing)
• – Uploaded, classified, and tracked documents in Veeva Vault eTMF
• – Maintained audit trails and version control
• – Structured TMF filing for Phase I–III trials
• – Understood CDM system integration with eTMF
• Skills Gained: Veeva Vault, TMF Management, Regulatory Compliance, Document Workflow, Audit Trails

Languages

• English, Hindi, Kannada, Telugu, Tamil

Skills

Keywords: Clinical Trial Protocol Interpretation, CRF Design, Medidata Rave, Oracle Clinical, Electronic Data Capture, CTMS, ICH-GCP Guidelines, Data Cleaning, Clinical Document Management, Attention to Detail, Problem-Solving, Communication, Documentation, Time Management

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Cover Letter:

Supriya
Bengaluru-560037

Hiring Manager
Panacea Medical Technologies Pvt. Ltd.
Mulur, kolar

Dear Hiring Manager,

I am writing to express my interest in the Clinical Research Associate (CRA) position at Panacea Medical Technologies. With a solid academic foundation in life sciences, hands-on analytical experience, and ongoing training in Clinical Data Management, I am eager to contribute to your clinical research team and advance innovative medical technologies.

I am currently pursuing my Master of Science at Reva University, building upon a B.Sc. in Life Sciences from Jyoti Nivas College. My recent internship at Fogiene Sciences provided practical experience in food and water quality analysis, NABL-compliant documentation, and laboratory procedures, sharpening my attention to detail and data accuracy. Additionally, I am undergoing certification in Clinical Data Management at Biotecnika, where I’ve gained exposure to tools like Medidata Rave and Oracle Clinical, alongside training in CRF design and GCP guidelines.

Your CRA role aligns perfectly with my career goals in clinical research and drug safety. I am particularly drawn to your emphasis on GCP compliance, data integrity, and collaboration with investigative sites—areas where I am confident my skills and training will be an asset. I bring strong communication skills, a commitment to ethical research practices, and a genuine passion for improving patient outcomes through high-quality clinical trials.

I would welcome the opportunity to contribute to Panacea’s mission and grow within your esteemed organization. Thank you for considering my application. I look forward to the possibility of discussing how I can support your clinical research initiatives.

Sincerely,
Supriya