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My professional strengths lie in my extensive experience as a Clinical Research Associate, particularly in managing global clinical trials across Phases I–IV. With over six years in sponsor-dedicated roles, I’ve honed my expertise in site management, risk-based monitoring, and ensuring adherence to Good Clinical Practice (GCP) guidelines. My proactive approach and analytical thinking enable me to consistently deliver high-quality results in clinical research.

I excel in project management, having coordinated global teams to ensure timely site activations, monitoring, and smooth trial progression. My skills in regulatory and quality compliance are vital in resolving protocol deviations efficiently while safeguarding patient safety and data quality. Technical proficiency is another strong suit—I’m adept at using platforms like Medidata Rave, Oracle InForm, and Veeva Vault eTMF, alongside tools like CTMS and laboratory portals for trial management.

Training and mentorship are areas I’m passionate about. I’ve successfully mentored Clinical Research Associates and conducted structured training for site staff, ensuring clarity in study protocols. I also have extensive experience in pharmacy monitoring, investigational product accountability, and documentation review for audit readiness.

With a diverse background in therapeutic areas, strong collaboration skills, and a proven ability to anticipate challenges, I am confident in my ability to drive operational success and contribute meaningfully to the advancement of clinical trials