Aurosmita Awain

Dedicated Clinical Research Coordinator with a proven track record at Curaclin, excelling in electronic data capture and fostering team growth. Demonstrated expertise in enhancing patient safety and ensuring compliance with ICH/GCP and FDA regulations. Skilled in streamlining processes for efficient study completion, with a focus on meticulous documentation and adverse event reporting.

Developed robust understanding of clinical research in fast-paced healthcare environment, managing multiple projects with precision. Demonstrated expertise in regulatory compliance and patient interaction, ensuring seamless project execution. Seeking to transition these transferable skills to new field, leveraging solid foundation in research and data analysis.

Personable and reliable, with strong foundation in clinical practices and patient care. Well-versed in regulatory compliance and data management, with solid grasp of clinical trial protocols. Dedicated to ensuring integrity and efficiency of clinical research projects and contributing to meaningful advancements in healthcare.

• Collaborated with team of [Number] in the development of [Project name].
• Achieved [Result] by introducing [Software] for [Type] tasks.
• Achieved [Result] by completing [Task] with accuracy and efficiency.
• Achieved [Result] through effectively helping with [Task].
• Documented and resolved [Issue] which led to [Results].
• Supervised team of [Number] staff members.

• Medical Device Regulatory Affairs Certification – RAPS or TOPRA.
• HIPAA Compliance Training Certificate – Various Accredited Providers.
• Certificate in Patient Recruitment – ACRP or SoCRA Specific Courses.
• Advanced Grant Writing Certificate–Various Universities and Organizations.