Senior Clinical Research Professional

Há 10 horas


Belo Horizonte, Brasil beBeeClinicalResearch Tempo inteiro

Job Title: Contract Clinical Research Associate About the Role We are seeking a detail-oriented and experienced clinical research professional to monitor and manage phase 2 seizure study clinical trials. The successful candidate will ensure the trial is conducted in compliance with regulatory standards, Good Clinical Practice (GCP), and the study protocol. Key Responsibilities Conduct site qualification, initiation, interim monitoring, and close-out visits. Evaluate site performance and provide corrective actions as necessary. Maintain accurate and up-to-date records of trial data and progress. Qualifications Bachelor's degree in Life Sciences, Nursing, or a related field. At least 2-4 years of experience as a Clinical Research Associate in oncology trials, with preference for Phase 2 experience. Strong knowledge of GCP, FDA regulations, and ICH guidelines. Experience with electronic data capture (EDC) systems and clinical trial management systems (CTMS). Preferred Qualifications Previous experience in early-phase oncology trials (e.g., dose escalation studies, first-in-human trials). Strong understanding of pharmacokinetics (PK) and pharmacodynamics (PD) assessments. About Us Our organization is dedicated to advancing medical research and improving patient outcomes. We offer a collaborative and dynamic work environment, with opportunities for professional growth and development.



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