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Clinical Data Management Associate II

Clario -
Remote

Apply Now

Job details

Full-time

Qualifications

Microsoft Word
Microsoft Excel
Microsoft Access
Computer Science
Relational databases
Bachelor's degree
Organisational skills
Communication skills

Full job description

Clario, a part of Thermo Fisher Scientific, is seeking a Clinical Data Management Associate II to support the review and evaluation of clinical data generated from the imaging components of sponsor clinical trials across multiple therapeutic areas. This role is responsible for delivering accurate, timely, and consistent clinical data to internal teams and client organizations in support of project and business objectives. The Associate II helps define and execute data management workflows for assigned projects, ensuring appropriate data quality control measures are applied throughout the study lifecycle.

What We Offer

Competitive compensation and benefits
The opportunity to work remotely within the United Kingdom
A collaborative, global environment supporting professional growth and development

What You’ll Be Doing

Review project documentation and requirements for new studies and anticipate impacts to Data Management (DM) standards and processes
Collaborate with cross‑functional project teams to stay informed of changes affecting data collection, cleaning, and data transfers
Support study implementation and data collection activities in alignment with project requirements
Define, run, and review edit checks; identify and resolve data discrepancies
Maintain organized, complete, and current study documentation
Create and/or review study Transmittal Forms, ensuring alignment with established standards
Keep the supervisor informed of project status, risks, and milestones
Review clinical data to identify errors and inconsistencies
Develop study data specifications, including data transfer specifications, system configuration specifications, and data validation rules
Partner with project teams to resolve data issues and track outstanding actions through to resolution
Prepare and validate ad hoc data listings as required
Ensure system bugs and enhancement needs are reported to the appropriate Product Manager and that any interim programming solutions are approved
Adhere to departmental processes, standards, and applicable Standard Operating Procedures (SOPs)
Participate in the review and updating of SOPs related to Data Management
Collaborate with internal colleagues to resolve issues and support team objectives
Contribute ideas to improve processes and add value to the organization
Support team success by assisting others as needed
Participate in relevant company‑sponsored training to maintain technical and industry knowledge
Perform other duties as assigned

What We Look For

Bachelor’s degree in Computer Science, Life Sciences, or a related field preferred, or equivalent relevant experience
Approximately one year of experience in a comparable role within the pharmaceutical, biotechnology, or CRO industry
Working knowledge of relational database organization and data validation principles
Experience with office productivity tools such as Microsoft Word, Excel, and Access preferred
Understanding of clinical trial terminology
Demonstrated problem‑solving ability
Ability to work independently while contributing effectively within a team environment
Strong attention to detail and organizational skills
Effective interpersonal and communication skills, both written and verbal
Professional, positive approach with the ability to adapt to changing priorities

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 starting your clinical data career or building long‑term expertise, your work helps bring life‑changing therapies to patients faster.

Apply Now

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