Clinical Research Associate I

To support clinical operations, the full-time remote In-House Clinical Research Associate I will manage trial monitoring, assist with compliance reporting, and collaborate with cross-functional teams throughout all phases of clinical studies. Key responsibilities Partner with study sites and cross-functional teams to support various trial elements Conduct remote monitoring of clinical trials and serve as a secondary contact for sites Ensure proper reporting and follow-up of serious adverse events (SAEs) and address non-compliance issues Required qualifications Experience in Neurology or Psychiatry, particularly with Schedule I controlled substances, is preferred Bachelor's degree in a clinical, biological, scientific, or health-related field, or equivalent experience 3 to 5 years of practical experience in clinical trials or proven experience in primary job functions Participation in study-specific meetings and training as needed Excellent English verbal and written communication skills