Clinical Data Management Associate II

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.

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

What You’ll Be Doing:

• 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

Ensure the accuracy and consistency of clinical databases by:

• 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

Additional responsibilities:

• 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

What We Look For:

• 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
• Familiarity with SAS is desirable
• 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

Working Conditions:

• Travel: 0–15%
• Lifting: 0–25 lbs
• Other: Computer-based work for extended periods of time

At Clario, 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.

Clario is an equal opportunity employer. Clario evaluates qualified applicants without regard to race, color, religion, gender, national origin, age, sexual orientation, gender identity or expression, protected veteran status, disability/handicap status, or any other legally protected characteristic.