Sign upLog in

Oncology CTMS Analyst

CAREERXCHANGE, Inc.

Miami, FL

Apply
JOB DETAILS
SALARY
$25–$33 Per Hour
SKILLS
Analysis Skills, Clinical Data, Clinical Information, Clinical Information Systems, Clinical Research, Clinical Support, Clinical Trial, Clinical Trial Management, Communication Skills, Customer Support/Service, Data Quality, Detail Oriented, FDA Requirements, Financial Regulations, GCP (Good Clinical Practices), Health Science, Leadership, Maintain Compliance, Microsoft Excel, Microsoft Office, Oncology, Operational Support, Operations Research, Organizational Skills, Problem Solving Skills, Process Improvement, Quality Monitoring, Reconciliation, Reporting Dashboards, Reporting Skills, Team Player, Time Management
LOCATION
Miami, FL
POSTED
4 days ago
Location: Miami, FL
Job Type: 15-Week Contract
Schedule: Monday – Friday | 8:30 AM – 5:00 PM
Pay: $25.00 – $33.00 per hour


Job Summary
We are seeking a detail-oriented Oncology CTMS Analyst to support a busy oncology research program during a 15-week contract assignment. The ideal candidate will have experience working with Clinical Trial Management Systems (CTMS) and oncology clinical research operations. This role is responsible for maintaining accurate study data, supporting clinical trial workflows, generating reports, and ensuring data integrity across multiple oncology research studies.


Responsibilities
  • Maintain and update clinical trial information within the Clinical Trial Management System (CTMS).
  • Ensure accurate tracking of study milestones, participant enrollment, and protocol activities.
  • Review, validate, and reconcile clinical research data for accuracy and completeness.
  • Generate reports and dashboards to support research operations and leadership.
  • Collaborate with investigators, research coordinators, finance, and regulatory teams.
  • Support study activation, maintenance, and closeout activities within the CTMS.
  • Monitor data quality and resolve discrepancies in a timely manner.
  • Ensure compliance with institutional policies, sponsor requirements, FDA regulations, and Good Clinical Practice (GCP) guidelines.
  • Assist with process improvement initiatives and CTMS optimization projects.
  • Provide user support and training related to CTMS functionality as needed.

Qualifications
  • Bachelor's degree in Health Sciences, Information Systems, Clinical Research, or a related field preferred.
  • Minimum of 2 years of experience working with a Clinical Trial Management System (CTMS).
  • Previous experience supporting oncology clinical research strongly preferred.
  • Knowledge of FDA regulations, Good Clinical Practice (GCP), and clinical research processes.
  • Strong analytical, organizational, and problem-solving skills.
  • Advanced proficiency in Microsoft Excel and Microsoft Office.
  • Excellent communication skills and ability to work collaboratively in a fast-paced environment.

CAREERXCHANGE, INC is an EOE.  Visit our website at www.careerxchange.com to view other job opportunities. 

About the Company

C

CAREERXCHANGE, Inc.