Clinical Data Management Associate II

• Review study documentation and project requirements to assess impacts on Clinical Data Management processes, standards, and deliverables.
• Collaborate with cross-functional teams to support study setup, data collection strategies, and evolving project requirements.
• Support the implementation and execution of data management plans for assigned imaging studies.
• Define, execute, review, and maintain edit checks to identify discrepancies and ensure high-quality clinical data.
• Review clinical and imaging-related data to identify inconsistencies, trends, and data quality issues.
• Develop and maintain study data specifications, including data transfer specifications, system configuration specifications, and data validation requirements.
• Create, review, and maintain transmittal forms and study documentation while ensuring compliance with established standards.
• Collaborate with project teams to investigate and resolve data discrepancies and outstanding issues.
• Track data-related issues through resolution and ensure timely follow-up with relevant stakeholders.
• Prepare, validate, and deliver ad hoc data listings and study reports as required.
• Identify system enhancements, bugs, or process improvement opportunities and coordinate communication with appropriate Product Management teams.
• Maintain complete, accurate, and audit-ready study documentation throughout the study lifecycle.
• Communicate project status, risks, and data quality concerns to supervisors and project stakeholders.
• Contribute to departmental process improvement initiatives, SOP updates, and quality enhancement activities.
• Support compliance with company procedures, Good Clinical Practice requirements, and applicable regulatory expectations.

What We Look For

• Bachelor's degree in Computer Science, Life Sciences, Healthcare, Clinical Research, Data Science, or a related field preferred, or equivalent professional experience.
• Minimum 3 or 3+ years of experience in Clinical Data Management, clinical research, biotechnology, pharmaceutical, CRO, or related healthcare environments.
• Understanding of clinical trial processes, data review methodologies, and clinical database management principles.
• Working knowledge of relational database concepts, data validation techniques, and quality control processes.
• Experience developing or maintaining data specifications, edit checks, data transfer requirements, or study configuration documentation preferred.
• Familiarity with clinical trial terminology and regulated research environments.
• Proficiency with Microsoft Office applications, including Word, Excel, Access, Outlook, and PowerPoint.
• Strong analytical and problem-solving skills with the ability to identify and resolve data quality issues.
• Excellent attention to detail and commitment to data accuracy and quality.
• Strong organizational, documentation, and time-management skills.
• Excellent verbal and written communication skills with the ability to communicate effectively in English.
• Ability to work independently while collaborating effectively within cross-functional and global teams.
• Professional, proactive, and customer-focused approach with a commitment to continuous improvement.
• At Clario, a part of Thermo Fisher Scientific, our purpose is to transform lives by unlocking better evidence.
• It’s a cause that unites and inspires us.
• It’s why we come to work and how we empower our people to make a positive impact every day.
• Whether you're advancing clinical science, building innovative technology, or supporting our global teams, your work helps bring life-changing therapies to patients faster.