Clinical Research Associate

Responsibilities

• Conduct site selection, initiation, routine monitoring, and close-out visits in accordance with GCP, ICH, and study requirements.
• Partner with clinical sites to develop and manage patient recruitment and enrollment strategies.
• Provide protocol training, ongoing support, and regular communication to investigators and site staff.
• Monitor study progress, regulatory submissions, data quality, and site performance while identifying and escalating risks.
• Maintain essential study documentation, including Trial Master Files (TMF) and Investigator Site Files (ISF), and support site financial management activities.

Requirements

• 3+ years of clinical research monitoring experience with a focus on oncology studies.
• Strong knowledge of Good Clinical Practice (GCP), ICH guidelines, clinical trial regulations, and oncology protocols.
• Excellent communication, organization, problem-solving, and relationship management skills with proficiency in Microsoft Office Suite.
• Bachelor’s degree in a scientific discipline, life sciences, healthcare, or a related field preferred.

Compensation

Salary Range: $90,000 - $130,000 depending on experience
Full Benefits Package: PTO, Paid Holidays, Medical, Dental, Vision, 401K, Tuition Reimbursement, Sick Leave as required by law

Keywords

• Clinical Research Associate
• CRA
• Oncology Research
• Clinical Trials
• GCP
• ICH Guidelines
• Site Monitoring
• TMF
• ISF
• Patient Recruitment
• Clinical Operations
• Regulatory Compliance
• Oncology Studies
• Monitoring Visits
• Pharmaceutical Research
• Biotechnology
• Clinical Development
• Remote Clinical Research Jobs
• Trial Management
• Investigator Site Management