Open to opportunities

Iqram Khan

@iqramkhan

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Clinical research professional experienced in Phase I–IV trials and regulatory compliance.

India

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What I'm looking for

I seek clinical operations roles where I can apply GCP-compliant trial coordination, patient recruitment, EDC/CTMS expertise, and grow into larger monitoring or project management responsibilities in a collaborative research environment.

I am a clinical research professional with an M.Sc. in Clinical Research and hands-on experience across Phase I–IV trials, BA/BE studies, and multi-site investigations. I emphasize rigorous adherence to ICH-GCP, DCGI, and institutional ethics standards.

During internships and traineeships I coordinated site activities, performed source data verification, and abstracted clinical records into eCRFs, supporting timely database lock and maintaining trial integrity. I am proficient with Medidata Rave, Inform, IWRS, and CTMS for electronic data capture and patient randomization.

I have direct experience in patient recruitment, informed consent processes, SAE/SUSAR documentation, IP accountability, and TMF maintenance, and I have supported monitoring, query resolution, and regulatory submissions with zero audit findings in documented assignments.

I bring strong organizational and leadership skills demonstrated by coordinating large events and captaining a championship volleyball team, and I seek opportunities where I can contribute to high-quality clinical operations and continuous process improvement.