Fortrea is a leading global contract research organization (CRO) dedicated to scientific rigor and clinical development excellence. We provide a comprehensive range of clinical development, patient access, and technology solutions for pharmaceutical, biotechnology, and medical device customers across more than 20 therapeutic areas. Operating in over 90 countries, Fortrea is committed to transforming drug and device development for partners and patients worldwide.
The Medical Review Specialist will undertake primary and secondary medical reviews of cases, ensuring the highest standards of quality and compliance. This role involves assessing the seriousness, causality, and adverse event coding of cases, as well as providing training and support to the case processing team.
Primary Medical Review: Conduct thorough medical assessments of cases, including evaluating seriousness, labeling, causality, adverse event coding, and narrative reviews.
Data Management: Update and document daily case data and feedback in appropriate trackers and tools to facilitate effective tracking and workflow management.
Deliverable Accountability: Assume complete responsibility for all assigned deliverables, ensuring adherence to quality, compliance, and productivity SLAs and KPIs.
Training and Guidance: Provide training and guidance to the case processing team on medical aspects of case processing.
Quality Control: Perform secondary medical reviews (QC role) and retrospective reviews of cases (QA role) to measure quality, identify error trends, and determine training needs and areas for improvement.
Aggregate Review and Analysis: Conduct aggregate medical reviews and signal detection/analysis activities as required.
Client Relationship Management: Enhance existing client relationships and foster a culture of high customer service.
Process Improvement: Participate in process improvement initiatives across the organization.
Fortrea is actively seeking motivated problem-solvers and creative thinkers who share our passion for overcoming barriers in clinical trials. Our commitment to revolutionizing the development process ensures the swift delivery of life-changing therapies to patients in need. Join our exceptional team and thrive in a collaborative environment that nurtures personal growth and enables you to make a meaningful global impact.
Fortrea is proud to be an Equal Opportunity Employer. We strive for diversity and inclusion in our workforce and do not tolerate harassment or discrimination of any kind. Employment decisions are based on business needs and individual qualifications, without regard to race, religion, gender, sexual orientation, age, or any other legally protected characteristic. We encourage all to apply.
For more information about how we collect and store your personal data, please see our Privacy Statement.
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