Medical Research Data Manager - Transplant Compliance

200 UM Corp (Enterprise)

United States

On-site

USD 65,000 - 90,000

Full time

4 days ago
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Benefits offered by this job

Medical benefits
Tuition remission

Job summary

University of Miami is seeking a Research Data Manager (Medical) to support the Adult Transplantation and Cellular Therapy Program. The role focuses on collecting, validating, and submitting data to NMDP and CIBMTR, maintaining data quality, and coordinating with external partners.

The position requires independent work, strong organization, and attention to detail to ensure compliance with regulatory standards and study protocols.

Qualifications

  • Three years of relevant work experience in hematology/oncology, research compliance, or study coordination and auditing.
  • CITI Certification within 30 days of hire is required.
  • Strong communication and computer skills are required.
  • Professional certification/licensure in nursing, clinical research, or related fields is preferred.
  • High-level interpersonal skills are required.

Responsibilities

  • Gathers, abstracts and submits patient data per NMDP/CIBMTR requirements.
  • Maintains data integrity across TCTP databases and audit files.
  • Performs data validation, audits, and prepares reports for regulatory audits.
  • Coordinates with NMDP, CIBMTR and data coordinators from other institutions.
  • Trains other Data Managers and supports policy/SOP development.

Skills

Excellent communication
Interpersonal skills
Computer skills
English fluency

Education

AS or Bachelor's degree in nursing/healthcare/science
CITI Certification within 30 days
Professional certification/licensure preferred

Job description

University of Miami is seeking a Research Data Manager (Medical) to support the Adult Transplantation and Cellular Therapy Program. The role focuses on collecting, validating, and submitting data to NMDP and CIBMTR, maintaining data quality, and coordinating with external partners.

The position requires independent work, strong organization, and attention to detail to ensure compliance with regulatory standards and study protocols.

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