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Clario logo
Clario

Transforming Lives by Unlocking Better Evidence | Decentralized clinical trials | Broadest endpoint technology

Clinical Data Manager

Data ScientistData ScientistFull TimeRemoteJuniorTeam 5,001-10,000Since 1973H1B SponsorCompany SiteLinkedIn

Location

Hungary

Posted

119 days ago

Salary

0

Seniority

Junior

Bachelor Degree1 yr expEnglish

Job Description

Clinical Data Manager

Clario

• Review and evaluate clinical data generated from the imaging portion of sponsor clinical trials across various therapeutic areas. • Perform all data management deliverables for assigned studies, ensuring timelines and quality standards are met. • Support study setup activities, including eCRF/TF design, database structure, and specifications, obtaining and providing necessary approvals. • Understand study implementation and data collection requirements and translate these into robust data management plans. • Collaborate with project teams to develop and maintain study-specific edit check criteria. • Define, run, and review edit checks, identify discrepant data, and drive timely data query resolution. • Coordinate, document, and oversee the receipt and processing of electronic or ancillary data from external sources (e.g., central labs, CROs, sponsors). • Maintain organized, complete, and up-to-date study documentation in accordance with internal and regulatory standards. • Track outstanding data issues, follow up with stakeholders, and ensure discrepancies are resolved and documented. • Ensure accuracy and consistency in the manipulation, review, and validation of clinical data, adhering to relevant regulatory guidelines. • Adhere to Clinical Data Management procedures, policies, and SOPs, and contribute to the review and improvement of departmental standards and processes. • Collaborate with internal teams to resolve operational issues, share knowledge, and support others in achieving project goals. • Participate in company-sponsored training to maintain and enhance technical and industry knowledge.

Job Requirements

  • Bachelor’s degree in Computer Science, Life Sciences, or a related field, or equivalent relevant experience.
  • Approximately 1+ years of experience in a similar role within the pharmaceutical, biotechnology, or CRO industry.
  • Working knowledge of relational database organization and data validation.
  • Familiarity with SAS is desirable.
  • Experience with office productivity tools such as Word, Excel, and Access.
  • Understanding of clinical trial terminology is an advantage.
  • Demonstrated problem-solving skills and a proactive, solution-oriented mindset.
  • Ability to work independently within a team environment and to adapt to changing priorities.
  • Excellent attention to detail with strong documentation and organizational skills.
  • Strong interpersonal and communication skills, both verbal and written.
  • Ability to project and maintain a professional, positive attitude while working with diverse stakeholders.

Benefits

  • Competitive compensation
  • Attractive benefits (security, flexibility, support and well-being)
  • Engaging employee programs
  • Remote working and home office allowance
  • OTP Szép Card

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