Data Manager, Clinical Research - 252252

Benefits

Qualifications

• •The ideal candidate is detail-oriented, adaptable, and skilled at navigating diverse personalities while maintaining a high standard of operational excellence
• •Minimum of 5 years of clinical research experience, preferably within an academic or high-volume research setting
• •Hands-on data entry and data management experience within clinical trials
• •Strong understanding of clinical trial processes, including working with sponsors and monitors
• •Proven ability to problem-solve and manage competing priorities in a fast-paced environment
• •Experience working directly with physicians and cross-functional clinical teams
• •Exceptional interpersonal and communication skills
• •Strong attention to detail and commitment to data integrity
• •Proactive, solutions-oriented mindset with the ability to anticipate needs and resolve issues independently
• •Highly organized with the ability to manage multiple studies and team priorities simultaneously
• •Collaborative leadership style with a focus on team development and support
• •8 more items(s)

Responsibilities

• •An oncology research site is seeking a highly organized and people-focused Data Core Manager to lead a team of data coordinators supporting complex oncology clinical trials
• •This individual will play a critical role in overseeing day-to-day data operations, ensuring high-quality data management practices, and serving as a central point of collaboration across clinical research teams
• •This role is heavily focused on team leadership and cross-functional coordination
• •Provide direct oversight and leadership to a team of data coordinators, including training, mentorship, workload distribution, and performance management
• •Serve as the primary resource for data-related questions, troubleshooting issues and ensuring timely resolution across studies
• •Collaborate closely with study coordinators, project managers, investigators, sponsors, and clinical research associates (monitors)
• •Oversee data entry, validation, and quality control processes to ensure accuracy and compliance with study protocols and regulatory requirements
• •Partner with internal teams to support study start-up, conduct, and closeout activities from a data perspective
• •Coordinate with sponsors and monitors during site visits, audits, and ongoing study communications
• •Identify process improvement opportunities and implement best practices to enhance data workflow efficiency and team productivity
• •Balance and allocate workload across the data team to support a high-volume, complex clinical trial portfolio
• •8 more items(s)