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A clinical research organization in Porto Alegre is seeking a detail-oriented Clinical Research Associate to manage Phase 2 seizure study clinical trials. This role involves collaborating with investigators, site personnel, and cross-functional teams to ensure participant safety and regulatory compliance. A Bachelor's degree in Life Sciences or Nursing and 2-4 years of relevant experience in oncology trials are required. The position offers an opportunity to work in a dynamic environment centered on trial integrity and compliance.
Contract Clinical Research AssociateWe seek a detail-oriented CRA to monitor and manage Phase 2 Seizure study clinical trials.
This position involves collaborating with investigators, site personnel, and cross-functional teams to ensure the safety and well-being of participants. Site Management and Monitoring: Conduct site qualification, initiation, interim monitoring, and close-out visits. The primary objective of this role is to ensure compliance with regulatory standards and Good Clinical Practice (GCP) guidelines, while ensuring the integrity of the trial data. Key Responsibilities include:
A Bachelor's degree in Life Sciences, Nursing, or a related field, along with at least 2-4 years of experience as a Clinical Research Associate in oncology trials, are required for this position.