Clinical Data Management Lead | Remote & Impactful

eResearch Technology Inc; United States; Remote; USD 120,000 - 170,000; Full time

Benefits offered by this job

Competitive compensation

Benefits focused on health, well-being

Flexible work arrangements

Employee development and recognition

Remote collaboration resources

Job summary

Clario, a part of Thermo Fisher Scientific, is seeking a Manager, Data Management to lead data management operations and ensure timely, high-quality clinical trial services. You will mentor staff, collaborate with sponsors and cross-functional teams, and drive process improvements in a global remote environment.

You will develop staff, monitor metrics, and ensure adherence to SOPs and regulatory requirements while advancing data integrity and patient safety across studies.

Qualifications

• Bachelor's degree in Life Sciences or a related field preferred.
• Minimum of four years of Clinical Data Management experience or equivalent industry experience.
• Prior people management experience, including leadership of direct reports and performance management responsibilities.
• Experience partnering directly with pharmaceutical, biotechnology, or clinical research sponsors.
• Strong knowledge of clinical trial processes, clinical data management practices, and regulatory requirements.
• Demonstrated ability to manage multiple priorities and balance operational, client, and people leadership responsibilities.
• Strong organizational, analytical, and problem-solving skills.
• Excellent written and verbal communication skills with the ability to influence stakeholders at all organizational levels.
• Experience developing and tracking operational metrics and performance indicators.
• Proficiency with Microsoft Office applications, including Outlook, Word, and Excel.
• Ability to build collaborative relationships across global teams and functions.
• Experience supporting process improvement initiatives and driving operational consistency across teams.
• Ability to work remotely and successfully lead distributed teams across multiple locations.

Responsibilities

• Lead and oversee Data Management operations to ensure timely, high-quality delivery of clinical trial services.
• Partner with sponsors and internal stakeholders to ensure study requirements, timelines, and quality expectations are achieved.
• Coordinate activities with Data Management leadership and cross-functional operational teams.
• Develop, implement, and maintain department procedures and process improvements to drive operational excellence.
• Monitor, analyze, and report departmental metrics and performance indicators.
• Determine staffing strategies and hiring projections to support business objectives.
• Manage, mentor, and develop Data Management staff, including performance evaluations, goal setting, and career development activities.
• Conduct regular department and team meetings to communicate priorities, performance, and organizational updates.
• Support the development and delivery of training programs and continuing education initiatives.
• Ensure adherence to global SOPs, working practice guides, and regulatory requirements.
• Oversee preparation for client audits, inspections, and internal quality reviews.
• Collaborate with Project Management and Operations teams to ensure consistent and effective data collection processes.
• Meet with clients to discuss protocol requirements, study strategy, and data management solutions.
• Support implementation of new systems, technologies, and operational processes.
• Promote collaboration across departments to optimize resource utilization and customer satisfaction.

Skills

People management

Data management

Cross-functional collaboration

Communication

Regulatory knowledge

Education

Bachelor's degree in Life Sciences or related field

Tools

Microsoft Office

Job description

Clario, a part of Thermo Fisher Scientific, is seeking a Manager, Data Management to lead data management operations and ensure timely, high-quality clinical trial services. You will mentor staff, collaborate with sponsors and cross-functional teams, and drive process improvements in a global remote environment.

You will develop staff, monitor metrics, and ensure adherence to SOPs and regulatory requirements while advancing data integrity and patient safety across studies.