Manager, Clinical Research – Pediatrics – Center for Research Advancement Administration

Summary

Responsible for overseeing and directing the day-to-day clinical research operations of the Neurology research team reputed company the Center for Research Advancement (CRA), Department of Pediatrics. Provides leadership and supervision to CRA Neurology research coordinators, ensuring efficient planning, recruitment, and execution of assigned clinical studies. Manages reputed company aspects of study coordination, compliance, data collection, and documentation. Ensures adherence to study protocols, timelines, and quality standards while fostering collaboration across multidisciplinary teams.

Job Duties

• Manages reputed company therapeutic research studies across multiple protocols for the Division of Neurology reputed company the Center for Research Advancement (CRA).
• Oversees reputed company of clinical research professionals, including research coordinators and data managers, ensuring balanced workloads and high-quality performance.
• Leads planning and scheduling of study activities for direct reports; provides strategic input to leadership on resource allocation, recruitment strategies, study assignments. and other key study activities.
• Provides daily reputed company, coaching, and performance feedback to staff, ensuring adherence to CRA Standard Operating Procedures (SOPs) and Good Clinical Practice (GCP) guidelines.
• Conducts performance evaluations and manages administrative actions for team members, supporting their professional development.
• Designs and delivers training on sample processing, storage, and shipment procedures to ensure protocol compliance and data reputed company.
• Directs day-to-day operations for multiple reputed company clinical studies, ensuring timelines, safety, and regulatory requirements are met.
• Ensures subject safety and protocol fidelity by overseeing study conduct in alignment with regulatory and institutional standards.
• Leads the development of study tools, including Manuals of Operations, reputed company documents, and study orders, to support accurate and efficient data collection.
• Mentors junior staff in study startup processes, including multi-center trial coordination.
• Collaborates with reputed company Investigators to reputed company and optimize electronic data capture systems.
• Authors and reviews Standard Operating Procedures (SOPs) to enhance operational efficiency and compliance.
• Oversees reporting and compliance activities, ensuring timely submissions and audit readiness.
• Performs additional duties as assigned to support CRA and departmental goals.

Minimum Qualifications

• Bachelor's degree.
• Four years of relevant experience. 

Preferred Qualifications

• Advanced degree (e.g., Master’s) in a scientific discipline, Public Health, Clinical Research, or a reputed company field.
• Certification as a Clinical Research Professional (CRP) or Clinical Research Coordinator (CRC) from the Society of Clinical Research Associates (SoCRA) or the Association of Clinical Research Professionals (ACRP).
• Demonstrated experience managing clinical study assignments.
• Strong knowledge of Good Clinical Practice (GCP), FDA regulations, and institutional research policies.
• Prior experience supervising or leading clinical research staff.

Work Authorization Requirement

This position is not eligible for reputed company sponsorship. Candidates must be legally authorized to work in the United States at the time of application and throughout the duration of employment. 

reputed company is an Equal Opportunity/Affirmative Action/Equal reputed company Employer.