Manoj Kumar

verified-iconManoj Kumar

Senior Clinical Trials Lead / Medical Reviewer

Accomplished Clinical Research and Medical Review professional with 12+ years of global experience across Phase I–IV clinical trials. Proven expertise in clinical trial leadership, medical and data review, protocol evaluation, and regulatory submissions. Skilled in data accuracy assurance, patient safety evaluation, and GCP/ICH compliance. Adept at cross-functional collaboration, risk-based monitoring, and audit readiness, ensuring high-quality outcomes and scientific excellence across multiple therapeutic domains including Oncology, Cardiology, Neurology, and Autoimmune Disorders.

FORMERLY AT

Biogen Idec

LOCATION

Banglore,India

AVAILABILITY

Full Time

Skills

Argus Safety

CTMS

eCRF

eTMF

Excel Audit Logs

Medidata Rave

MS Excel (data tracking)

Oracle Clinical

Oracle CTMS

SAS Listings Viewer

TrialMaster

Work Experience

Senior Clinical Trials Lead / Medical Reviewer

Biogen Idec

Apr 2011 – Present

  • Lead global Phase II–III clinical programs across multiple therapeutic areas.

  • Perform clinical and medical data review of AE/SAE narratives, listings, and outputs for accuracy, logic, and consistency with study protocols.

  • Review and approve core clinical documents (Protocols, IBs, CRFs, ICFs, Clinical Study Reports).

  • Collaborate with data management and safety teams on signal detection, reconciliation, and medical escalations.

  • Conduct investigator meetings and protocol trainings to maintain quality and compliance.

  • Ensure audit readiness, GCP adherence, and execution of studies within timelines and budgets.

  • Support statistical review for outlier detection, data trends, and risk-based monitoring.

TECHNOLOGIES

Medidata Rave, Oracle Clinical, eTMF, CTMS, Argus Safety, MS Excel (data tracking), SAS Listings Viewer

Project Manager – Clinical Operations & Medical Review

PFC Pharma Focus AG

Apr 2010 – Apr 2011

  • Oversaw global Phase II/III studies ensuring alignment between clinical, medical, and regulatory teams.

  • Managed cross-functional project timelines, data integrity, and safety consistency across submissions.

  • Provided medical review inputs to PV and QA teams to ensure regulatory compliance and readiness.

  • Led risk management and data quality improvement initiatives within operational frameworks.

TECHNOLOGIES

Oracle Clinical, CTMS, eTMF, Medidata, Clinical Portal

Associate Program Manager – Clinical Data & Safety Review

University of New South Wales

Aug 2009 – Jan 2010

  • Conducted medical review and QC of clinical data for signal detection and reporting accuracy.

  • Supported regulatory documentation preparation and submission compilation.

  • Collaborated with investigators and data management to resolve data inconsistencies.

  • Ensured data accuracy aligned with ICH-GCP and local regulatory standards.

TECHNOLOGIES

Medidata Rave, MS Access, Safety Database Systems, Excel Trackers

Clinical Site Manager / Lead CRA (Medical Oversight)

PPD Inc.

Jan 2009 – Jul 2009

  • Oversaw site-level data quality, SAE reconciliation, and ensured regulatory adherence.

  • Reviewed clinical data for medical plausibility and protocol adherence.

  • Acted as liaison between medical monitors, safety teams, and investigative sites.

  • Supported audit preparation and data verification for inspection readiness.

TECHNOLOGIES

Oracle CTMS, eCRF, Medidata Rave, TrialMaster, Excel Audit Logs

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