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Nadeem Akhtar

@nadeemakhtar1

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Clinical Research Coordinator at IQVIA who coordinated three concurrent cardio-metabolic and oncology trials.

Canada

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At IQVIA, I coordinated three concurrent clinical trials across cardio-metabolic and oncology indications under Principal Investigator delegation. I maintained Health Canada and ICH-GCP compliance and ongoing inspection readiness.

At Fresno Clinical Research Center, I implemented risk-based monitoring plans across nine trials and built Key Risk Indicator dashboards to flag data anomalies and missing entries. I also reduced protocol deviations through staff training and electronic informed consent workflows.

Experience

Work history, roles, and key accomplishments

Clinical Research Site Coordinator

IQVIA

Sep 2025 - Jul 2026 (10 months)

Led day-to-day coordination of 3 concurrent clinical trials in cardio-metabolic and oncology, maintaining 100% compliance with Health Canada and ICH-GCP standards. Directed cross-functional teams and prioritized budget allocation to protect study timelines.

Clinical Trials ICH GCP Health Canada Regulations Risk Based Monitoring Cross functional Leadership Budget Management Audit Readiness

Clinical Research Coordinator III

Fresno Clinical Research Center

Aug 2020 - Jul 2025 (4 years 11 months)

Implemented risk-based monitoring plans across 9 trials in cardio-metabolic, GI/MASH, and nephrology, reducing protocol deviations by 90% and improving patient retention by 88%. Built KRI dashboards that reduced data queries by 90%.

Risk Based Monitoring ICH GCP Electronic Informed Consent Patient Retention Data Management KRI Dashboards Corporate Trainer

Clinical Research Coordinator II

North America Research Institute Inc.

May 2014 - May 2019 (5 years)

Designed and implemented safety monitoring plans for oncology and nephrology protocols, ensuring timely adverse event reporting. Co-established a cross-functional Data and Safety Monitoring Board and standardized regulatory submissions achieving 100% ICH-GCP compliance.

Safety Monitoring Adverse Event Reporting DSMB Regulatory Submissions IRB ICH GCP