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Clario

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

Clinical Data Manager

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

Location

United States

Posted

93 days ago

Salary

0

Seniority

Junior

Bachelor Degree1 yr expExperience acceptedEnglish

Job Description

Clinical Data Manager

Clario

• Performing all data management deliverables for assigned studies • Attending and participating in client meetings as requested • Understanding study requirements for implementation and data collection • Collaborating with project teams to develop study-specific edit check criteria • Defining, running, and reviewing edit checks and resolving discrepant data • Maintaining organized, complete, and up-to-date study documentation • Performing study setup activities, including database structure, specifications, and approvals • Coordinating and documenting the receipt and processing of electronic or ancillary data received from external sources such as central laboratories, CROs, or sponsors • Keeping supervisors informed of project status and potential issues • Ensure the accuracy and consistency of clinical databases by: • Reviewing clinical data and identifying errors or inconsistencies • Collaborating with project teams to resolve data issues • Tracking outstanding issues and following up until resolution • Ensuring that clinical data management activities comply with regulatory guidelines and study protocols • Additional responsibilities: • Adhere to Clinical Data Management procedures, policies, and work instructions • Read, understand, and follow applicable Standard Operating Procedures (SOPs) • Assist in establishing and maintaining departmental standards • Participate in the review and update of company SOPs related to Data Management services • Work with internal teams to resolve issues and support operational goals • Contribute to team success by supporting colleagues and sharing knowledge • Participate in company-sponsored training and maintain awareness of industry best practices • Perform additional tasks and responsibilities as assigned

Job Requirements

  • Bachelor’s Degree in Computer Science, Life Sciences, or a related field preferred, or equivalent experience
  • At least 1+ year of experience in a similar role within the pharmaceutical, biotech, or CRO industry
  • Working knowledge of relational database organization and validation
  • Familiarity with SAS is desirable
  • Experience with Microsoft Office tools including Word, Excel, and Access
  • Understanding of clinical trial terminology and processes
  • Strong problem-solving skills and analytical thinking
  • Excellent attention to detail and data accuracy
  • Strong interpersonal, written, and verbal communication skills
  • Strong documentation and organizational abilities
  • Ability to work independently while collaborating effectively within a team
  • Ability to manage changing priorities in a fast-paced environment
  • Ability to maintain a professional and positive attitude

Benefits

  • Competitive compensation
  • Private health insurance
  • Engaging employee programs
  • Flexible work schedules
  • Attractive PTO plan
  • Flex workspace

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