
Personable and organized individual with strong multitasking abilities and excellent communication skills. Familiar with office software and data entry .Committed to supporting team efficiency and ensuring smooth operations.
• Operated the weighbridge system to weigh and record vehicle and load weights accurately.
· Assisted in the coordination and execution of clinical trials in accordance with GCP (Good Clinical Practice) and study protocols.
· Collected, recorded, and entered clinical data from participant files and case report forms (CRFs) into relevant databases.
· Supported participant recruitment, screening, and informed consent processes under supervision.
· Maintained accurate and confidential participant records and ensured secure handling of sensitive data.
· Helped prepare study-related documentation, including regulatory binders and ethics submissions.
· Collaborated with study nurses, investigators, and coordinators to ensure smooth day-to-day operations.
· Participated in monitoring visits, quality control checks, and internal audits.
· Ensured study supplies and samples were correctly labeled, stored, and transported.
Time Management
Attention to Detail
Confidentiality & Professionalism
Strong Communication (written & verbal)
Team Collaboration
Multitasking Under Pressure
Problem Solving
Adaptability
Critical Thinking
Organizational Skills
Work Ethic & Reliability
Ability to Follow Protocols & Procedures
Database Administration (eg REDCap, Medidata, or internal systems)