Medical Data Review Associate Manager
Fortrea
Medical Data Review Associate Manager
Fortrea
Global CRO providing Phase I-IV trials
Job Overview:
The Associate Medical Data Review Manager is an important member of the Global Medical Review Team with responsibility for execution of key Central Medical Review activities within the Central Monitoring strategy, such as: Collaborate within a matrix environment, communicate proactively internally and externally and across functions with key stakeholders to ensure Central Monitoring/Central Medical Review Plans is proactively and effectively executed to meet client expectations. Responsible for the preparation and conduct of Central Medical Review tasks across a series of sponsor projects commencing with Xcellerate® Medical Review tool launch up to and including the study report. Conduct reviews of Central Medical Review under guidance of a Central Medical Review Plan and communicates findings at the site, patient level. This review is performed with oversight by the Project Physician who also acts as an escalation point for the Medical Reviewer-Central Monitoring. Provide Central Medical Review support to the study team and to the client.
Summary of Responsibilities:
Qualifications (Minimum Required):
Experience (Minimum Required):
Physical Demands/Work Environment:
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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.
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