Sr Clinical Research Associate (Sr CRA) - Ophthalmology-Remote

Responsibilities: The role is accountable for performance and compliance for assigned protocols and sites, ensuring adherence to regulations and quality standards. The Sr CRA acts as the primary site contact and manager throughout all phases of a clinical research study.

Requirements: Candidates must have at least 7 years of relevant experience in healthcare, including 4 years of direct site management experience, and 5 years of ophthalmology experience. A degree in a scientific or healthcare discipline is required, with a preference for those with a bachelor's degree or higher.

Key skills: Adverse Event Report, Clinical Data Management, Clinical Development, Clinical Research, Clinical Research Organizations Management, Clinical Study Management, Clinical Trial Compliance, Clinical Trial Documentation, Clinical Trial Management, Clinical Trial Planning, Clinical Trials Monitoring, Regulatory Affairs Compliance, Site Management, Preventive Action

Keywords: Clinical Research, Ophthalmology, Site Management, Monitoring, ICH/GCP, Regulatory Compliance, Clinical Trials, Data Management, Patient Recruitment, Quality Control, Adverse Events, Clinical Development, SOPs, CTMS, eTMF, Pharmacovigilance