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A leading global contract research organization in Veracruz, Mexico, is looking for a dedicated candidate to support medical review processes. Responsibilities include ensuring regulatory compliance, managing Medical Review tools, and collaborating with stakeholders to drive process improvements. The ideal candidate should excel in data analysis and communication, with a commitment to fostering diversity and inclusion in the workplace. Candidates from all backgrounds are encouraged to apply.
As a leading global contract research organization (CRO) with a passion for scientific rigor and decades of clinical development experience, Fortrea provides pharmaceutical, biotechnology, and medical device customers a wide range of clinical development, patient access and technology solutions across more than 20 therapeutic areas.
With over 19,000 staff conducting operations in more than 90 countries, Fortrea is transforming drug and device development for partners and patients across the globe.
Collaborates in the development of Central Monitoring proposal text and review of costing, contributes to proposal strategy and development when Central Medical Review is included.
Fortrea is proud to be an Equal Opportunity Employer :
As an EOE / AA employer, Fortrea strives for diversity and inclusion in the workforce and does not tolerate harassment or discrimination of any kind.
We make employment decisions based on the needs of our business and the qualifications of the individual and do not discriminate based upon race, religion, color, national origin, gender (including pregnancy or other medical conditions / needs), family or parental status, marital, civil union or domestic partnership status, sexual orientation, gender identity, gender expression, personal appearance, age, veteran status, disability, genetic information, or any other legally protected characteristic.
We encourage all to apply.
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