Senior Clinical Research Associate (Fully Remote)

Senior Clinical Research Associate overseeing complex clinical studies. Responsible for training, mentoring, and coordinating junior CRAs. Key liaison between investigators, site staff, and project teams. Key Responsibilities: Prepare, conduct, and report site selection, initiation, monitoring, and closeout visits. Perform CRF reviews, source document verification, and clinical data query resolution. Support audit preparation and assist Regulatory Affairs teams with documentation. Requirements: College or university degree in Life Sciences or equivalent experience. At least 3 years of independent, on-site clinical monitoring experience. Full professional proficiency in Spanish and English. Tailored training courses and professional mentoring for career development. Opportunity to develop skills in training, mentoring, and leadership. Exposure to complex clinical studies and potential progression to Lead Monitor. Not Disclosed The partner company is a clinical research organization specializing in complex clinical studies. It fosters a people-focused culture with opportunities for professional growth and mentoring. #J-18808-Ljbffr Not Disclosed