Top 49425 Sub Jobs | SimplyHired

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Clinical Research- Sub Investigator ANP/PA

Aton Health -
Kansas City, MO

Quick Apply

Job Details

Full-time
$100,000 - $125,000 a year

Benefits

Health savings account
Health insurance
Dental insurance
401(k)
Paid time off
Vision insurance
Life insurance

Qualifications

Gastroenterology
Clinical research
Care documentation
Nurse Practitioner (NP)
Attention to detail
Clinical assessment documentation
Advanced practice provider
Healthcare diagnosis
Medical terminology
Physician Assistant License

Full Job Description

Company Overview

Aton Health is a clinician-led, participant-first research company rethinking how evidence is generated in modern healthcare. Instead of treating trials as separate from care, we embed research directly into real-world clinical workflows, helping sponsors and specialty practices accelerate enrollment, improve study execution, and generate high-quality, audit-ready evidence at scale. Our model depends on operational precision and regulatory rigor. We’re building a team that takes pride in executing with accuracy and where compliance is embedded in every step of the process.

Position Summary

The Sub Investigator (Nurse Practitioner or Physician Assistant) serves as a key clinical member of the research team, supporting the Principal Investigator (PI) in the conduct of clinical trials. This individual is responsible for ensuring the safety and medical oversight of study participants, adherence to protocol requirements, and the integrity of clinical data.

The Sub Investigator will perform clinical assessments, support participant eligibility determination, oversee study-related medical procedures, and contribute to the accurate and timely documentation of clinical findings. This role requires strong clinical judgment, attention to detail, and the ability to operate within a highly regulated research environment while delivering high-quality patient care.

Key Responsibilities

Clinical Oversight and Participant Safety

Perform clinical evaluations, including medical history review, physical examinations, and ongoing participant assessments
Monitor participant safety throughout the study, including identification and documentation of adverse events (AEs) and serious adverse events (SAEs)
Provide medical oversight during study visits and ensure appropriate clinical decision-making
Escalate clinical concerns to the Principal Investigator as needed

Study Conduct and Protocol Execution

Support the PI in ensuring all study activities are conducted in accordance with the protocol, GCP, and regulatory requirements
Assess and confirm participant eligibility based on protocol criteria
Perform study-related procedures within scope of licensure (e.g., physical exams, lab review, medication management as applicable)
Collaborate with Clinical Research Coordinators to ensure accurate and timely execution of study visits

Documentation and Data Quality

Ensure accurate, complete, and timely documentation of all clinical findings in source documents and EDC systems
Review and sign off on clinical data as required
Support query resolution and data clarification requests from sponsors or CROs
Maintain audit-ready documentation at all times

Participant Engagement and Care

Serve as a clinical resource for study participants, addressing questions and concerns related to their care and study participation
Ensure informed consent is appropriately obtained and documented (as delegated)

Quality and Regulatory Compliance

Ensure compliance with IRB-approved protocols, HIPAA, FDA regulations, and ICH-GCP guidelines
Participate in monitoring visits, audits, and inspections as needed
Support quality assurance activities and continuous improvement initiatives
Maintain appropriate licensure, certifications, and training required for study conduct

Qualifications

Required

Current, active licensure as a Nurse Practitioner (NP) or Physician Assistant (PA)
Graduate of an accredited NP or PA program
2+ years of clinical experience in a healthcare setting
Strong clinical assessment and diagnostic skills
Knowledge of medical terminology and clinical documentation standards

Preferred

Prior experience in clinical research or as a Sub Investigator
Familiarity with GCP, FDA regulations, and clinical trial processes
Experience with electronic medical records (EMR) and electronic data capture (EDC) systems
Experience in specialty areas relevant to active or planned studies

Competencies

Strong clinical judgment and decision-making ability
High attention to detail and commitment to data integrity
Ability to balance patient care with protocol adherence
Effective communication and collaboration with cross-functional teams
Professionalism and confidence in interacting with participants, sponsors, and site staff
Strong organizational and time management skills
Integrity and commitment to ethical research practices

Physical Demands

The physical demands described here are representative of those that must be met by an employee to successfully perform the essential functions of this job.

While performing the duties of this job, the employee is regularly required to talk or hear. The employee must occasionally lift and or move up to 10 pounds. The employee frequently is required to stand; walk; use hands to finger, handle or feel; and reach with hands and arms.

AAP/EEO Statement

The Company is an equal opportunity employer. In accordance with anti-discrimination law, it is the purpose of this policy to effectuate these principles and mandates. The Company prohibits discrimination and harassment of any type and affords equal employment opportunities to employees and applicants without regard to race, color, religion, sex, national origin, disability status, protected veteran status, or any other characteristic protected by law. The Company conforms to the spirit as well as to the letter of all applicable laws and regulations.

Other Duties

Please note this job description is not designed to cover or contain a comprehensive listing of activities, duties or responsibilities that are required of the employee for this job. Duties, responsibilities and activities may change at any time with or without notice.

Pay: $100,000.00 - $125,000.00 per year

Benefits:

401(k)
Dental insurance
Health insurance
Health savings account
Life insurance
Paid time off
Vision insurance

Work Location: Hybrid remote in Kansas City, MO 64114

Quick Apply

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