Clinical Research Associate

Qualifications 

• Bachelor's degree in life science/related field, advanced degree preferred.
• Minimum of 4+ years in the clinical research industry.
• Proven track record in managing clinical trials and site monitoring.
• In-depth knowledge of clinical trial processes, GCP, and regulatory requirements.
• Strong organizational, leadership, and time-management skills.
• Excellent communication, problem-solving, and interpersonal abilities.
• Ability to handle complex issues and provide effective solutions.
• Capacity to work with and review large volumes of documentation and data.
• Ability to travel to and from clinical sites and manage site visit requirements.
• Combination of office work and travel to clinical sites, which may include healthcare environments and other clinical settings.

Responsibilities 

• Plan and conduct routine monitoring visits to evaluate site performance and compliance with study protocols, GCP, and regulatory standards.
• Oversee and support site staff in the execution of the study, including resolving complex issues and ensuring adherence to timelines.
• Perform site initiation, interim monitoring, and closeout visits.
• Review and verify source data against case report forms (CRFs) and other study documentation for accuracy and completeness.
• Identify, address, and resolve data discrepancies and issues.
• Ensure that data collection processes are efficient and compliant with protocol requirements.
• Ensure that clinical trials are conducted in accordance with regulatory requirements, including FDA guidelines, ICH GCP, and local regulations.
• Prepare and review essential documents and study records, ensuring compliance with regulatory standards.
• Assist in preparing for and managing audits and inspections.
• Provide training and support to junior CRAs and site staff on study protocols, procedures, and regulatory requirements.
• Mentor and guide less experienced team members, fostering professional development and ensuring high-quality performance.
• Act as a primary point of contact for study sites, addressing complex issues and facilitating communication between site staff and the study team.
• Collaborate with the study team to provide updates on site performance, study progress, and any issues or risks.
• Coordinate with cross-functional teams to ensure that study milestones and deliverables are met.
• Prepare detailed monitoring visit reports and ensure timely submission of site documentation.
• Assist in the preparation of study documentation, including protocols, amendments, and study reports.
• Maintain organized and accurate records of monitoring activities and site communications.