Gulam Mohammed
@gulammohammed
Senior clinical data management leader delivering end-to-end DM excellence for global, complex trials.
What I'm looking for
I’m a Senior Lead Clinical Data Manager with 10+ years of progressive clinical data management experience, including 5+ years leading large, complex global clinical studies and multi-program portfolios. I’m recognized as a trusted client partner and strategic contributor who elevates quality, operational rigor, and proactive risk mitigation across cross-functional and vendor-partner environments.
In my current role at Merck, I lead end-to-end Clinical Data Management activities across global Phase II–III and late-phase programs, serving as Program Lead/DTL/SME and primary client liaison for DM deliverables. I own governance and close-out frameworks, lead Data Management Plan development, oversee eCRF/database build and validation strategies, and drive quality governance through real-time monitoring, deviation assessments, RCA, and CAPA—supporting audit readiness and inspection outcomes.
I’ve also built strong delivery capabilities across the full DM lifecycle at LABCORP and PPD, including database design/build oversight, UAT coordination, production release approvals, interim deliverables, and final database lock readiness. From earlier roles at TCS and Cognizant, I developed foundational proficiency in DM systems, workflows, and GCP/regulatory expectations, and I now mentor junior and mid-level DM professionals to strengthen organizational capability.
Experience
Work history, roles, and key accomplishments
Leads end-to-end clinical data management across multiple global Phase II–III and late-phase programs, ensuring delivery excellence, regulatory alignment, and quality governance. Serves as primary client liaison and program lead, overseeing DMPs, eCRF/database build activities, vendor integrations (including SAE reconciliation), audit readiness, and financial governance (SOW/change orders and invo
Provides full life-cycle clinical data management leadership for multiple global Phase I–IV trials, ensuring compliant execution, quality governance, and stakeholder alignment. Manages DMPs and study documentation, oversees database build and UAT coordination through database lock planning, and supports inspection/audit readiness and CAPA management.
Clinical Data Manager
PPD
Nov 2018 - Feb 2020 (1 year 3 months)
Supports operational execution of clinical data management across multiple trials, including structured workflows for data capture and compliance. Performs data review and query oversight, supports SAE reconciliation and external vendor data integration, and contributes to database lock readiness through interim deliverables, listings review, and UAT participation.
Assists senior clinical data managers with executing clinical trial data management workflows to support accurate data capture and timely delivery. Supports CRF review cycles, discrepancy resolution, vendor data reconciliation, and UAT execution for eCRF environments while maintaining SOP/GCP compliance and audit documentation readiness.
Begins career in clinical data management by supporting foundational operational tasks such as data review verification, query support, and documentation maintenance. Maintains CRF tracking logs and operational files, supports vendor coordination and reporting, and develops baseline knowledge of GCP and CDM lifecycle processes.
Education
Degrees, certifications, and relevant coursework
Jawaharlal Nehru Technological University
Master's Degree, Pharmaceutical Sciences
2012 - 2014
Master’s degree in Pharmaceutical Sciences from Jawaharlal Nehru Technological University (2012–2014).
RJPV
Bachelor's Degree, Pharmaceutical Sciences
2008 - 2012
Bachelor’s degree in Pharmaceutical Sciences from RJPV (2008–2012).
Tech stack
Software and tools used professionally
Availability
Location
Authorized to work in
Job categories
Skills
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