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Clinical Research Coordinator/ Patient Coordinator

AXLE INFORMATICS · Baltimore, MD · posted 10 days ago

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30
Certified filings · by AXLE INFORMATICS, FY2026 Q2
$126,152
Median filed wage · across all this employer’s sponsored roles

Source: US DOL Office of Foreign Labor Certification, LCA disclosure data, FY2026 Q2. Government data is published roughly one quarter in arrears.

No single filed job title matched this advert closely enough, so the figure above is AXLE INFORMATICS’s median across every role it sponsored.

The figure above is not this job’s salary. It is what AXLE INFORMATICS reported to the US Department of Labor for the closest role it has sponsored. A filing history means this employer has sponsored before — it is not a promise that this opening carries sponsorship, and not an offer of pay. Check the advert and ask the employer.

See every role AXLE INFORMATICS has sponsored, and what it paid →

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The role, as AXLE INFORMATICS describes it

(ID: 2026-3812)

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 Institute on Drug Abuse (NIDA) located in Baltimore, 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 NIDA's clinical research operations. The role involves screening and scheduling study participants, obtaining informed consent, and administering mental health assessments and diagnostic interviews. The coordinator will also collect and manage research data, maintain regulatory documentation, and serve as a liaison between participants and investigators. The role involves extensive participant contact, including the collection and handling of biological specimens. The work schedule may include weekends and nights. Candidates must have a Master's degree in psychology, social work, biological sciences, or a related discipline. They also need a minimum of three years of experience in a research-related field and a minimum of one year of experience in behavioral counseling, preferably in drug, smoking, or alcohol treatment. Basic Life Support (BLS) certification is required, and training will be provided.

Additional Qualifications

Certifications & Licenses

  • Basic Life Support (BLS) certification (training will be provided)

Field of Study

  • Masters Degree in Psychology, Social Work, or Social Sciences - Required
  • LMSW - Preferred

Software

  • Microsoft Office
  • Electronic medical records system
  • REDCap

Skills

  • Minimum of one year of experience in behavioral counseling, preferably in drug, smoking, or alcohol treatment - Required
  • Minimum of three years of experience in a research-related field
  • Previous experience interacting with human subjects in a clinical or research setting
  • Previous clinical trial work
  • Excellent analytical, organizational, and time management skills
  • Strong oral and written communication skills
  • Exceptional interpersonal skills, with a customer service-oriented and client-focused approach due to extensive participant contact
  • Ability to complete all NIH/NIDA mandatory trainings and other required trainings by the deadlines set

Deliverables

  • Work products and documents related to administering mental health assessments and diagnostic interviews — Ad-Hoc
  • Work products and documents related to obtaining participant medical and drug use information according to protocol criteria — Ad-Hoc
  • Work products and documents related to obtaining informed consent documentation from participants in the screening protocol — Ad-Hoc
  • Work products and documents related to follow-up correspondence with study candidates on recruiting status — Ad-Hoc
  • Work products and documents related to arranging travel and distributing remuneration for study candidates — Ad-Hoc
  • Work products and documents related to phone screen scripts, in-person screening appointment

Read the full advert and apply on AXLE INFORMATICS’s site →

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