Clinical Research Associate (CRA) - Oncology (Remote)

Responsibilities: The Clinical Research Associate (CRA) is responsible for ensuring compliance with study protocols and managing site relationships throughout all phases of clinical research. This includes monitoring site performance, conducting visits, and collaborating with various stakeholders to support assigned sites.

Requirements: Candidates must have at least 5 years of relevant experience in healthcare, including 2 years of direct site management experience, or a bachelor's degree with 2 years of experience. An associate's degree or equivalent in a scientific or healthcare discipline is also acceptable.

Key skills: Clinical Research, Site Management, Monitoring, Good Clinical Practice, Data Analysis, Regulatory Compliance, Oncology, Pharmacovigilance, Problem Solving, Communication, Time Management, Organizational Skills, Adaptability, Accountability, Conflict Management, Documentation Practices

Keywords: Clinical Research, Oncology, Site Management, Monitoring, Good Clinical Practice, Data Analysis, Regulatory Compliance, Pharmacovigilance, Clinical Trials, Adverse Event Reporting, Clinical Study Management, Clinical Trial Planning, Documentation Practices, IT Applications, Patient Recruitment, Quality Standards