Psicro is seeking a detail-oriented Clinical Data Monitor to remotely review study data, identify errors and systemic issues, and generate data queries to ensure data integrity and participant safety. You will support risk-based and central monitoring activities, contribute to inspection readiness, and collaborate with a general team to maintain study quality.
Ideal candidates hold a Bachelor's degree with at least 1 year in Clinical Research; CEFR B2 English or higher and strong MS Office skills