Jobs and Careers

Clinical Research Coordinator

United Statesfull_timeVerifiedPosted 23 Jul 2026

💰 $155,000/yr($145,000/yr – $155,000/yr)

About the role

(ID: 2026-2879)

Axle is a bioscience and information technology company that offers advancements in translational research, biomedical informatics, and data science applications to research centers and healthcare organizations nationally and abroad. With experts in biomedical science, software engineering, and program management, we focus on developing and applying research tools and techniques to empower decision-making and accelerate research discoveries. We work with some of the top research organizations and facilities in the country including multiple institutes at the National Institutes of Health (NIH).

Axle is seeking a Clinical Research Coordinator to join our vibrant team at the National Institutes of Health (NIH) supporting the National Cancer Institute (NCI) located in Bethesda, MD.

Benefits We Offer:

100% Medical, Dental & Vision Coverage for Employees
Paid Time Off and Paid Holidays
401K match up to 5%
Educational Benefits for Career Growth
Employee Referral Bonus
Flexible Spending Accounts:
- Healthcare (FSA)
- Parking Reimbursement Account (PRK)
- Dependent Care Assistant Program (DCAP)
- Transportation Reimbursement Account (TRN)

Position Overview

Clinical Research Coordinator, NCI: The National Cancer Institute (NCI), Office of the Clinical Director (OCD), supports the conduct of intramural clinical research focused on cancer and related diseases. The OCD provides the infrastructure required to conduct high-quality clinical research in a safe patient care environment, including protocol review, regulatory oversight, clinical informatics, data management, quality assurance, and clinical operations support. The Government requires contractor support to provide comprehensive clinical research coordination services for oncology and cancer-related clinical trials conducted within the NCI Intramural Research Program. Requires a Bachelor's degree in Nursing, Biological Sciences, Public Health, Health Sciences, Clinical Research, or a related field.

Additional Qualifications

Certifications & Licenses

Bachelor's degree in Nursing, Biological Sciences, Public Health, Health Sciences, Clinical Research, or related field

Field of Study

Nursing
Biology
Community and Public Health

Software

Experience with electronic medical records, clinical trial management systems, and electronic data capture platforms

Skills

Experience supporting oncology clinical trials and clinical research operations
Knowledge of FDA regulations, ICH-GCP, human subjects protections, and clinical trial methodology
Strong organizational, communication, and project coordination skills
Demonstrated experience supporting clinical trials from startup through closeout

Deliverables

Enrollment and Accrual Reports — Monthly
Protocol Activity Status Reports — Monthly
Regulatory Tracking Reports — Monthly
Data Quality and Query Resolution Reports — Monthly
Monitoring Visit Support Documentation — Ad-Hoc
Specimen Tracking Logs — Daily
Study Supply Inventory Reports — Quarterly
Study Closeout Documentation — Ad-Hoc
Final Technical Summary Report — Ad-Hoc

Statement of Work Details

Provide guidance and operational training to junior staff, trainees, students, and temporary personnel as requested by the Government — 1
Assist with onboarding activities related to protocol operations and study procedures — 2
Support continuity of operations and knowledge transfer efforts — 3
Collect, review, validate, and enter research data into approved electronic systems — 4
Collaborate with data management personnel to ensure data quality and completeness — 5
Maintain inventories of study supplies, kits, equipment, and research materials
Verify case report forms (CRFs) and source documentation
Resolve sponsor, monitor, and data management queries
Perform routine data quality control activities
Generate study reports, workload reports, enrollment reports, and data