Regional Monitor

Overview

• Serve as a Clinical Research Monitor overseeing clinical trials and ensuring compliance with protocols and regulatory requirements.
• Collaborate with investigators, research organizations, and institutions to expedite clinical studies and maintain effective communication.
• Review adverse event cases, monitor timelines, budgets, and schedules, and prepare detailed study documentation.
• Provide training to investigators and site personnel on clinical trial protocols and procedures.
• Implement clinical development strategies and contribute to the design and monitoring of evaluation projects.
• Ensure patient recruitment and retention for clinical trials, maintaining adherence to Good Clinical Practices (GCP).
• Work remotely with occasional travel to support clinical trial sites and stakeholders.

Key Responsibilities & Duties

• Monitor clinical trial progress at site and headquarters levels, ensuring adherence to protocols and regulatory standards.
• Develop and maintain relationships with clinical investigators, CROs, and affiliated institutions.
• Review adverse events, monitor project timelines and budgets, and issue detailed status reports.
• Train site personnel and investigators on clinical trial protocols and procedures.
• Assist in the design, development, and monitoring of clinical evaluation projects.
• Implement clinical strategies and recommend qualified investigators for clinical trials.
• Ensure patient recruitment and retention, maintaining compliance with GCP and SOPs.
• Collaborate with stakeholders to achieve project milestones and improve processes.

Job Requirements

• Bachelor of Science (BS) degree required, preferably in a related field.
• Minimum of 4 years of experience in clinical research monitoring; 6 years preferred.
• Proficiency in Microsoft Systems, RAVE, and CTMS platforms.
• Ability to travel extensively by plane, train, or automobile as required.
• Strong knowledge of Good Clinical Practices (GCP) and regulatory requirements.
• Experience in training investigators and site personnel on clinical protocols.
• Capability to manage project timelines, budgets, and deliverables effectively.
• Excellent communication skills for collaboration with internal and external stakeholders.