Clinical Data Management Associate II

Clinical Data Management Associate II 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 OfferCompetitive compensation and benefitsThe opportunity to work remotely within the United KingdomA collaborative, global environment supporting professional growth and developmentWhat You'll Be DoingReview project documentation and requirements for new studies and anticipate impacts to Data Management (DM) standards and processesCollaborate with cross-functional project teams to stay informed of changes affecting data collection, cleaning, and data transfersSupport study implementation and data collection activities in alignment with project requirementsDefine, run, and review edit checks; identify and resolve data discrepanciesMaintain organized, complete, and current study documentationCreate and/or review study Transmittal Forms, ensuring alignment with established standardsKeep the supervisor informed of project status, risks, and milestonesReview clinical data to identify errors and inconsistenciesDevelop study data specifications, including data transfer specifications, system configuration specifications, and data validation rulesPartner with project teams to resolve data issues and track outstanding actions through to resolutionPrepare and validate ad hoc data listings as requiredEnsure system bugs and enhancement needs are reported to the appropriate Product Manager and that any interim programming solutions are approvedAdhere to departmental processes, standards, and applicable Standard Operating Procedures (SOPs)Participate in the review and updating of SOPs related to Data ManagementCollaborate with internal colleagues to resolve issues and support team objectivesContribute ideas to improve processes and add value to the organizationSupport team success by assisting others as neededParticipate in relevant company-sponsored training to maintain technical and industry knowledgePerform other duties as assignedWhat We Look ForBachelor's degree in Computer Science, Life Sciences, or a related field preferred, or equivalent relevant experienceApproximately one year of experience in a comparable role within the pharmaceutical, biotechnology, or CRO industryWorking knowledge of relational database organization and data validation principlesExperience with office productivity tools such as Microsoft Word, Excel, and Access preferredUnderstanding of clinical trial terminologyDemonstrated problem-solving abilityAbility to work independently while contributing effectively within a team environmentStrong attention to detail and organizational skillsEffective interpersonal and communication skills, both written and verbalProfessional, positive approach with the ability to adapt to changing prioritiesAt 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.