Travel Sub-Investigator

CARE

Sub-Investigator responsible for travel and tele-medicine support in clinical research for Care Access. Engaging in trial execution and patient management responsibilities.

Posted 6/29/2026full-time🇺🇸 United StatesMid-LevelSenior💰 $130,000 - $165,000 per yearWebsite

Core Competencies

Role fit

Core Competencies

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Demonstrates expertise in clinical research protocols, including the administration of investigational products and monitoring of adverse events. Holds a Master's Level Science Degree and possesses strong clinical experience as a Nurse Practitioner or Physician Assistant.

Highest-signal resume keywords

Clinical Research ExperienceInfusion SkillsetSub-Investigator ExperienceLicensure in Good StandingPatient Assessment

ATS Keywords

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Applicant Tracking System Keywords

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Hard Skills

Administration of Investigational ProductsIntravenous Line MaintenancePhysical ExaminationsAdverse Event ReportingClinical Protocol Compliance

Certifications & Qualifications

Master’s Level Science DegreeNurse Practitioner LicensePhysician Assistant License

Industry Keywords

Clinical ResearchStudy ProtocolsRegulatory CompliancePatient MonitoringClinical Practice

About the role

Key responsibilities & impact

Work closely with the Principal Investigator to oversee the execution of study protocols.
Delegating study related duties to site staff, as appropriate, and ensuring site compliance with study protocols.
Complies with regulatory requirements, policies, procedures, and standards of practice.
Be available to see subjects virtually or in-person as dictated by project design.
Administration of Investigational Products (via subcutaneous, transdermal, intramuscular, intravenous, or oral routes).
Proficiency in starting, monitoring, and maintaining intravenous lines.
Provide ongoing assessment of the study subject/patient to identify Adverse Events.
Ensure that serious and unexpected adverse events are reported promptly to the Pl.
Perform physical examinations as part of screening evaluation and active study conduct.
Other duties as assigned.

Requirements

What you’ll need

At least Master’s Level Science Degree. Nurse Practitioner or Physician Assistant with 5+ years of clinical experience.
Clinical practice experience desired with infusion skillset.
Currently licensed in good standing in one or more states.
A minimum of 1 year of relevant work experience as Sub-Investigator (preferred) in a Clinical Research setting.
Preferred at least one (1) year of experience as a Clinical Research Coordinator or willingness to learn.
You must have the authorization to work in the US for any employer.
You must not need visa sponsorship, either now or in the future.
You must live in the USA and be willing and able to travel with 24–36-hour notice

Benefits

Comp & perks

Paid Time Off (PTO) and Company Paid Holidays
100% Employer paid medical, dental, and vision insurance plan options
Health Savings Account and Flexible Spending Accounts
Bi-weekly HSA employer contribution
Company paid Short-Term Disability and Long-Term Disability
401(k) Retirement Plan, with Company Match