Location
buenos aires
Job Type
Full-time
Posted
June 17, 2026
Job Description
The Role
- Working independently and actively to coordinate activities to set up and monitor a study, completing accurate study status reports and maintaining study documentation
- Submission of protocol, consent documents for ethics/IRB approval and assist in preparing regulatory submissions as requested
- Participate in preparing and reviewing study documentation and feasibility studies for new proposals as required
- Balancing sponsor generated queries efficiently and responsible for study cost-effectiveness
- Dependent on level of experience you may assist in training and mentoring less expert CRA’s and/or lead CRA’s working on international projects
What you need
- 18months+ of monitoring experience in phaseI‑III trials as a CRA
- Knowledge of ICG GCP guidelines and expertise to review and evaluate medical data
- Excellent written and verbal communication skills in English
- Ability to pro...