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Fortrea

Global CRO providing Phase I-IV trials

Medical Data Review Associate Manager

Clinical Research OperationsConfirmed live in the last 24 hours
Full-timeBengaluru, Karnataka, IndiaNo salary listed

About the Job

Requirements

  • Medical doctors, allied medical degrees, postgraduate study in life sciences, or other applicable qualifications are required; relevant and equivalent experience may be considered in lieu of educational requirements.
  • Minimal travel is required.

Responsibilities

  • Collaborate within a matrix environment and communicate proactively with internal and external stakeholders across functions to ensure Central Monitoring and Central Medical Review Plans are effectively executed to meet client expectations.
  • Prepare and conduct Central Medical Review tasks across sponsor projects, from launch of the Xcellerate Medical Review tool through the study report.
  • Conduct Central Medical Reviews under guidance of a Central Medical Review Plan and communicate findings at the site and patient level, with oversight by the Project Physician, who acts as an escalation point for the Medical Reviewer-Central Monitoring.
  • Provide Central Medical Review support to the study team and client.
  • Collaborate in developing Central Monitoring proposal text and reviewing costing, and contribute to proposal strategy and development when Central Medical Review is included.
  • Support sponsor presentations and bid defenses.
  • Ensure tracking and status reporting are performed accurately and on time.
  • Apply data to recommend actions for patient safety concerns.
  • Identify and evaluate safety signals using individual cases, cumulative data assessments, and other signal detection systems.
  • Contribute to the Risk Assessment and Categorization Tool for medical-review topics and consider risks when planning Xcellerate Medical Review configuration.
  • Support the Data Expert with Critical Data and Process Definition and EDC design implementation.
  • Support development of medical review requirements, including visualization design and consideration of study data feeds such as EDC and laboratory data.
  • Draft and finalize the Central Medical Review Configuration Plan and maintain it throughout the study, including re-versioning as required.
  • Draft Central Monitoring and Central Medical Review Plans with the Central Monitoring Manager, when applicable, and Project Physician; update the plans throughout the study, including refinement of visualizations and changes to data.
  • Manage configuration of the Xcellerate Medical Review tool, program study-specific visualizations in the tool, and perform user acceptance testing.
  • Perform ongoing Central Medical Review, discuss findings with the Project Physician internally and/or with the client, ensure identified issues are followed to resolution, and write reports when required.
  • Act as a subject matter expert based on education and experience when applicable.
  • Make data-driven decisions and communicate findings proactively and effectively to key stakeholders.
  • Take responsibility for inspection readiness for medical assessment activities and support regulatory authority inspections when needed.
  • Collaborate with other Central Monitoring activities to ensure consistency and effectiveness.
  • Evaluate and collate process-improvement suggestions and submit them to leadership.
  • Evaluate and submit ideas and justifications for improved systems and tools to leadership.
  • Provide project and process training to new team members and mentor new team members.
  • Perform other duties as needed or assigned.
  • If acting as line manager, manage direct reports to ensure staff training records are current and utilization targets are met or exceeded according to job grade.
  • If acting as line manager, cascade relevant information from internal and external meetings to direct reports and appropriate colleagues.
  • If acting as line manager, assist with recruiting new staff.
  • If acting as line manager, ensure tools and machinery function properly and are maintained.
  • If acting as line manager, convey organizational problems to senior managers to inform their decisions.
  • If acting as line manager, manage performance reviews and issues for direct reports.
  • If acting as line manager, ensure the Central Monitoring department functions smoothly.

About the Company

Fortrea

Global CRO providing Phase I-IV trials

Fortrea is a global contract research organization that provides clinical development services for the life sciences industry. It offers full service, functional service, and hybrid outsourcing models across Phase I–IV trials, clinical pharmacology, and consulting, serving biotech, biopharma, medical devices, and diagnostics. Its work is delivered through a network of investigators and specialized teams in approximately 100 countries, supporting trial design, execution, data management, and regulatory compliance. Fortrea’s approach combines its legacy experience from Covance and Labcorp with a pureplay CRO model to deliver fit-for-purpose solutions and agile project delivery. This positions it to manage trials across more than 20 therapeutic areas with scientific rigor and operational excellence. The company aims to bring predictability to clinical trial execution and help clients turn research ideas into real-world outcomes.

Company size
10,001+
Company stage
IPO
Headquarters
Winston-Salem, NC
Founded
2023

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