Clinical Research Specialist Hematologic Malignancies Trials

University of Maryland, Baltimore

Baltimore (MD)

On-site

USD 70,000 - 100,000

Full time

4 days ago
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Job summary

The University of Maryland, Baltimore (UMB) Marlene & Stewart Greenebaum Comprehensive Cancer Center (UMGCCC) seeks a full-time Clinical Research Specialist for the Hematologic Malignancies program. You will screen, consent, and enroll patients, guide them through visits, and support data collection and analysis in cutting-edge therapeutic trials.

Collaborating with Principal Investigators and care teams, you will manage protocol development, HIPAA compliance, and study workflows, with some

Qualifications

  • Bachelor's degree in a scientific field related to clinical settings.
  • Three (3) years of clinical research experience including two (2) years in relevant specialization.
  • Substitution options: other education/experience with specified equivalencies.

Responsibilities

  • Screen, consent, and enroll subjects per protocol.
  • Coordinate IRB/HIPAA protocol development and compliance.
  • Interact with participants, collect medical histories, and obtain samples as needed.
  • Maintain databases and run data quality checks using Excel/Access.
  • Perform data analysis with SAS, SPSS, and R; manage data collection and interpretation.
  • Communicate protocol information with participants and team members.
  • Oversee daily clinical research operations and budgets; liaise with IRB and sponsors.
  • Assist in grants, publications, and research study design.

Skills

Clinical research
IRB/HIPAA
Data management
SAS/SPSS/R
Patient recruitment

Education

Bachelor's degree in a scientific field

Tools

SAS
SPSS
R
Excel/Access

Job description

The University of Maryland, Baltimore (UMB) Marlene & Stewart Greenebaum Comprehensive Cancer Center (UMGCCC) seeks a full-time Clinical Research Specialist for the Hematologic Malignancies program. You will screen, consent, and enroll patients, guide them through visits, and support data collection and analysis in cutting-edge therapeutic trials.

Collaborating with Principal Investigators and care teams, you will manage protocol development, HIPAA compliance, and study workflows, with some

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