Senior Clinical Research Professional

4 semanas atrás

Curitiba, Brasil beBeeClinicalResearch Tempo inteiro

Clinical Research Associate Role Conduct site visits, qualify sites, initiate trials, manage study files and provide instructions to personnel. Verify participant protection by confirming informed consent procedures and protocol adherence. Evaluate data integrity and compliance with approved protocols, GCP and SOPs. Duties: Coordinate investigative site staff to achieve trial deliverables. Verify proper management and accountability of investigational product. Write and submit reports on investigational site findings and update tracking systems. Qualifications: Bachelor's degree in a clinical or scientific field from an accredited institution. Healthcare professional licensure, e.g. registered nurse. Previous experience supporting clinical trials with solid onsite monitoring experience in CROs or pharmaceutical companies. Benefits and Perks: A competitive compensation package. A range of benefits focused on employee well-being and work-life balance opportunities.

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