Clinical Data Manager

Clario

1d

About The Position

The Clinical Data Manager is responsible for reviewing and evaluating clinical data generated from the imaging portion of sponsor clinical trials conducted across various therapeutic areas. This role supports the accuracy, integrity, and completeness of clinical trial databases by managing study data, performing edit checks, and collaborating with cross-functional project teams to resolve discrepancies. The Clinical Data Manager plays a key role in ensuring clinical data is collected, validated, and maintained in compliance with regulatory standards and study requirements. Through strong attention to detail, analytical thinking, and effective collaboration, this role contributes to the successful delivery of high-quality clinical trial data that supports critical research and development decisions.

Requirements

• Bachelor’s Degree in Computer Science, Life Sciences, or a related field preferred, or equivalent experience
• At least 1+ year of experience in a similar role within the pharmaceutical, biotech, or CRO industry
• Working knowledge of relational database organization and validation
• Experience with Microsoft Office tools including Word, Excel, and Access
• Understanding of clinical trial terminology and processes
• Strong problem-solving skills and analytical thinking
• Excellent attention to detail and data accuracy
• Strong interpersonal, written, and verbal communication skills
• Strong documentation and organizational abilities
• Ability to work independently while collaborating effectively within a team
• Ability to manage changing priorities in a fast-paced environment
• Ability to maintain a professional and positive attitude

Nice To Haves

• Familiarity with SAS is desirable

Responsibilities

• Performing all data management deliverables for assigned studies
• Attending and participating in client meetings as requested
• Understanding study requirements for implementation and data collection
• Collaborating with project teams to develop study-specific edit check criteria
• Defining, running, and reviewing edit checks and resolving discrepant data
• Maintaining organized, complete, and up-to-date study documentation
• Performing study setup activities, including database structure, specifications, and approvals
• Coordinating and documenting the receipt and processing of electronic or ancillary data received from external sources such as central laboratories, CROs, or sponsors
• Keeping supervisors informed of project status and potential issues
• Reviewing clinical data and identifying errors or inconsistencies
• Collaborating with project teams to resolve data issues
• Tracking outstanding issues and following up until resolution
• Ensuring that clinical data management activities comply with regulatory guidelines and study protocols
• Adhere to Clinical Data Management procedures, policies, and work instructions
• Read, understand, and follow applicable Standard Operating Procedures (SOPs)
• Assist in establishing and maintaining departmental standards
• Participate in the review and update of company SOPs related to Data Management services
• Work with internal teams to resolve issues and support operational goals
• Contribute to team success by supporting colleagues and sharing knowledge
• Participate in company-sponsored training and maintain awareness of industry best practices
• Perform additional tasks and responsibilities as assigned

Benefits

• Competitive compensation
• Private health insurance
• Engaging employee programs
• Flexible work schedules
• Attractive PTO plan
• Flex workspace

What This Job Offers

• Job Type: Full-time
• Career Level: Entry Level