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A global clinical research organization is seeking a dedicated individual to manage the Trial Master File. Responsibilities include maintaining and archiving documents, ensuring compliance with procedures, and reporting TMF completeness. Candidates should have a Bachelor’s degree, prior administrative experience, and proficiency in both English and Portuguese. Great organizational and time-management skills are a must.
Company Description
We are the company that cares – for our staff, for our clients, for our partners and for the quality of work we do. A dynamic, global company founded in 1995, we bring together more than 2,700 driven, dedicated and passionate individuals. We work on the frontline of medical science, changing lives, and bringing new medicines to those who need them.
Only CVs in English will be considered.
Our mission is to be the best CRO in the world as measured by our employees, clients, sites, and vendors. Our recruitment process is easy and straightforward, and we’ll be there with you every step of the way.