Clinical Research Data Manager I

• →Works on trials directly assigned. Works on industry sponsored trials which provide consistent monitoring/oversight.
• →Assist senior staff maintain high enrolling studies.
• →Accountable for all data management tasks in support of low complexity clinical research studies under direct supervision.
• →In collaboration with the principal investigator (PI), assists with collecting and reviewing documents such as medical records, while maintaining a high degree of confidentiality.
• →Participates in quality assurance reviews conducted by study sponsors, federal agencies, or specially designated internal review groups.
• →Prepares study-related documentation for analysis, such as protocol worksheets, adverse event reports, institutional review board documents, or progress reports.
• →Performs other related work as needed.

• Bachelors degree.

• Minimal medical/science related education or position.

• Absorb large amounts of information quickly.
• Adaptability to changing working situations and work assignments.
• Attention to detail.
• Interact and communicate (verbal and written) with clarity, tact, and courtesy with patrons, sponsors, staff, faculty, students, and others.
• Organizational skills.
• Read and understand complex documents.
• Time management.
• Ability to work independently and as part of a team.

• Resume/CV (required)
• Cover Letter (required)

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FLSA Status

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Pay Range

The included pay rate or range represents the University’s good faith estimate of the possible compensation offer for this role at the time of posting.

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