Clinical Data Management Associate II (Life Sciences)

TL;DR

Clinical Data Management Associate II (MedTech): Supporting the review and evaluation of clinical imaging data for sponsor clinical trials with an accent on data quality control, validation rules, and workflow execution. Focus on identifying data discrepancies, developing data transfer specifications, and ensuring alignment with clinical trial standards.

Location: Remote within the United Kingdom

Company

hirify.global, a part of Thermo Fisher Scientific, focuses on transforming lives by unlocking better evidence through clinical trial imaging and data solutions.

What you will do

• Review project documentation and define data management workflows for new clinical studies.
• Execute and review edit checks to identify and resolve data discrepancies.
• Develop study data specifications, including data transfer and system configuration rules.
• Collaborate with cross-functional project teams to ensure data quality throughout the study lifecycle.
• Maintain study documentation and prepare ad hoc data listings as required.
• Report system bugs and enhancement needs to Product Managers.

Requirements

• Bachelor’s degree in Computer Science, Life Sciences, or a related field (preferred).
• Approximately one year of experience in pharmaceutical, biotechnology, or CRO industry.
• Working knowledge of relational database organization and data validation principles.
• Proficiency in office productivity tools such as Microsoft Word, Excel, and Access.
• Must be based in the United Kingdom to work remotely.
• Strong attention to detail and effective interpersonal communication skills.

Culture & Benefits

• Competitive compensation and benefits package.
• Opportunity to work remotely within the UK.
• Collaborative, global environment supporting professional growth and development.