# Clinical Research Coordinator at Axle

> United States · Unspecified · Other · open. Source: https://alderhq.app/jobs/greenhouse%3Aaxle%3A5283252007 (read 2026-11-06).

## Facts (observed)

- Company: [Axle](https://alderhq.app/companies/axle)
- Location text: Bethesda, MD; Axle Informatics LLC
- Where it can be done from (inferred): United States (evidence: "Location: Bethesda, MD; Axle Informatics LLC")
- Posted: 2026-11-03 (3 days ago)
- First seen by alder: 2026-11-03 · last verified: 2026-11-04
- Reposted: 0 times · edited: 0 times
- Apply on the employer's site: https://job-boards.greenhouse.io/axle/jobs/5283252007

## Pay and sponsorship

- Posted pay: $145k–$155k per year (from the listing's pay field)
- Market band for similar posted roles (Washington DC, n 682): p25 $80k, median $113k, p75 $162k
- H-1B filings at this company for similar roles, FY25: 1 ([US DOL OFLC LCA disclosure data](https://www.dol.gov/agencies/eta/foreign-labor/performance))

## Description (the employer's text)

(ID: 2026-3938)

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

The Clinical Research Coordinator will support oncology and cancer-related clinical trials within the NCI Intramural Research Program. The role includes coordinating studies from startup through closeout, supporting participant recruitment and follow-up, managing research data and regulatory records, coordinating specimens and assessments, and supporting participant safety and protocol compliance.

Responsibilities

• Coordinate multiple clinical studies, supporting protocol activation, implementation, amendments, study conduct, and closeout in collaboration with investigators and study teams.

• Screen, recruit, assess eligibility, and schedule participants according to protocol criteria; support informed consent activities as authorized by the principal investigator (PI).

• Serve as a primary contact for participants and families, explain study procedures and investigational therapies, monitor adherence, and conduct study and survival follow-up.

• Coordinate visits, procedures, laboratory testing, imaging, and ancillary services within protocol-defined visit windows.

• Coordinate pharmacokinetic (PK), pharmacodynamic (PD), biomarker, quality-of-life (QoL), and patient-reported outcome (PRO) assessments, including questionnaires and interviews.

• Collaborate with clinical staff on blood specimens, electrocardiograms (ECGs), vital signs, measurements, wearable device data, and other protocol-required assessments.

• Maintain accurate source documentation and electronic medical record (EMR) entries; obtain and review outside medical records, pathology materials, imaging studies, and reports.

• Coordinate research specimen collection, processing, tracking, storage, and shipment; maintain chain-of-custody documentation and specimen accountability.

• Collect, validate, and enter research data; verify case report forms (CRFs), resolve queries, and perform quality control with data management staff.

• Maintain databases, trackers, and study metrics; prepare enrollment, workload, and study reports and support interim analyses and final reporting.

• Prepare regulatory submissions, continuing reviews, amendments, and closure documentation; maintain regulatory binders, delegation-of-authority logs, signatures, approvals, and submission deadlines.

• Assist with adverse event reporting and protocol deviation documentation, and maintain records ready for audits and inspections.

• Coordinate monitoring visits, prepare source and regulatory records, respond to findings, and track corrective actions.

• Support participant safety, help investigators evaluate responses to investigational therapies, and participate in multidisciplinary rounds and study meetings.

• Develop and maintain study tools, calendars, worksheets, and workflow documents; identify and resolve implementation issues and support documentation quality improvements.

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Data: alder (https://alderhq.app). Cite https://alderhq.app/jobs/greenhouse%3Aaxle%3A5283252007 and the date you read it. Observed facts come from the employer's own listing; location reach, level, family and skills are inferences.