Clinical Data Management Associate II

🕒 May 26

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Clario

WebsiteLinkedInAll Job Openings

5001 - 10000 employees

Founded 1973

⚕️ Healthcare Insurance

🧬 Biotechnology

🤖 Artificial Intelligence

💰 Private Equity Round on 2019-10

Healthcare Insurance • Biotechnology • Artificial Intelligence

Clario is a company specializing in accelerating clinical trials from initiation to implementation through advanced technologies and services. Since 2018, Clario has revolutionized endpoint analyses in clinical trials by integrating over 30 artificial intelligence-enabled solutions across more than 600 active trials, enhancing data quality and patient privacy while expediting data collection processes. Clario provides a comprehensive clinical trial management platform, offering solutions such as eCOA, cardiac safety, medical imaging, precision motion, and respiratory services in various therapeutic areas including oncology, cardiology, and neurology. Known for its global reach, Clario supports clinical trials in over 100 countries with a strong focus on decentralized and hybrid trial models. The company's commitment to patient safety and innovation is reflected in their over 26,000 trials and involvement in numerous new drug approvals.

📋 Description

• 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

🎯 Requirements

• 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.

🏖️ Benefits

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