IKIqram Khan
@iqramkhan
Clinical research professional experienced in Phase I–IV trials and regulatory compliance.
IndiaWhat I'm looking for
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.
Experience
Work history, roles, and key accomplishments
Clinical Research Coordinator
Clicebo Solutions Pvt. Ltd.
May 2025 - Jun 2025 (1 month)
Coordinated a multi-site retrospective medical device study across 3 hospitals, abstracting 500+ records into eCRFs and conducting structured patient follow-ups that improved follow-up compliance while maintaining full ICH-GCP and DCGI adherence with zero audit findings.
Clinical Research Trainee
Sun Pharma
Contributed to BA/BE studies by screening and consenting healthy volunteers, performing supervised venipuncture and PK sample handling, and ensuring investigational product dispensing with 100% protocol compliance per DCGI and ICH-GCP.
Clinical Research Trainee
Max Super Speciality Hospital
Managed patient randomizations via IWRS, supported SAE documentation and deviation reporting, and assisted monitoring activities and regulatory binder maintenance to uphold trial integrity.
Clinical Research Trainee
Batra Hospital & Medical Research Centre
Supported Phase III cardiology trial operations including CRF/eCRF documentation, ICF/TMF management, and use of EDC and IWRS for randomization, aiding query resolution and timely database lock in compliance with ICH-GCP.
Education
Degrees, certifications, and relevant coursework
JUJamia Hamdard University
Master of Science, Clinical Research
Activities and societies: Involved in clinical trial operations, site monitoring support, and trainee roles in hospital and industry settings.
Completed an M.Sc. in Clinical Research with practical experience in Phase I–IV trials, regulatory compliance, and electronic data capture systems.
JUJamia Hamdard University
Bachelor of Science, Medical Laboratory Technology
Activities and societies: Participated in clinical traineeships, sample handling, and trial support activities including venipuncture and IP dispensing.
Completed a B.Sc. in Medical Laboratory Technology with hands-on laboratory and clinical study support experience.
Tech stack
Software and tools used professionally
Availability
Location
IndiaAuthorized to work in
Job categories
Skills
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