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Arisa Health
Posted 11 days agoVerified live 11h ago

Research Coordinator

Brief overview

Remote
MastersOr in progress
2+ yrsMinimum
Clinical Research CoordinationHuman Subjects Research ProtectionsResearch EthicsHIPAARegulatory ComplianceData CollectionStudy DocumentationREDCapMicrosoft OfficePatient-Centered Outcomes ResearchCommunity-Engaged ResearchClinical Research Certification

About the company

Arisa Health logo
Arisa Healtharisahealth.org

Arisa Health provides outpatient, therapeutic foster care, counseling, substance abuse recovery inpatient, and mental health services.

Job description

Summary

Arisa Health is Arkansas' largest and most comprehensive nonprofit behavioral health provider. The Research Coordinator oversees the day-to-day implementation of a PCORI-funded research study at a community-based clinic, supervises a site-based research assistant, and ensures compliance with approved protocols and regulatory requirements. The role serves as the primary contact for site-level research operations and collaborates with participants, clinic staff, community partners, and the Johns Hopkins University study team.

Responsibilities

  • The Research Coordinator is responsible for overseeing the day-to-day implementation of a PCORI-funded research study at a community-based clinic, including the supervision of a site-based research assistant
  • This role ensures that all study activities are conducted in accordance with approved protocols, regulatory requirements, and patient-centered research principles
  • The Research Coordinator will serve as the primary point of contact for site-level research operations and will work closely with study participants, clinic staff, community partners, and the Johns Hopkins University (JHU) study team to support high-quality study execution

Skills

  • Master's degree in counseling or social work
  • Current Arkansas license (LPC / LCSW )
  • 2-5 years in related field required
  • Minimum of 2–3 years of experience coordinating clinical research, community-based research, or health-related projects
  • Knowledge of human subjects research protections, research ethics, HIPAA, and regulatory compliance requirements
  • Strong organizational skills with the ability to manage multiple responsibilities and deadlines
  • Demonstrated ability to work effectively with diverse patient populations and community stakeholders
  • Experience with data collection, study documentation, and electronic data capture systems
  • Proficiency in Microsoft Office applications and REDCap or similar research database platforms
  • Excellent written, verbal, and interpersonal communication skills
  • The ability to work effectively independently and with team members
  • Ability to establish and maintain effective working relationships with others
  • Willingness to complete required research training upon hire and pass proficiency quizzes
  • Experience with PCORI-funded studies, patient-centered outcomes research, or community-engaged research
  • Experience coordinating multi-site, federally funded, or clinic-based research studies
  • Familiarity with community-based participatory research (CBPR) or stakeholder-engaged research approaches
  • Experience working in a community health center, FQHC, or safety-net clinical setting
  • Clinical research certification such as SOCRA or ACRP, or willingness to obtain certification

Qualifications

Must Haves

  • Master's degree in counseling or social work
  • Current Arkansas license (LPC / LCSW )
  • 2-5 years in related field required
  • Minimum of 2–3 years of experience coordinating clinical research, community-based research, or health-related projects
  • Knowledge of human subjects research protections, research ethics, HIPAA, and regulatory compliance requirements
  • Strong organizational skills with the ability to manage multiple responsibilities and deadlines
  • Demonstrated ability to work effectively with diverse patient populations and community stakeholders
  • Experience with data collection, study documentation, and electronic data capture systems
  • Proficiency in Microsoft Office applications and REDCap or similar research database platforms
  • Excellent written, verbal, and interpersonal communication skills
  • The ability to work effectively independently and with team members
  • Ability to establish and maintain effective working relationships with others
  • Willingness to complete required research training upon hire and pass proficiency quizzes

Nice to Haves

  • Experience with PCORI-funded studies, patient-centered outcomes research, or community-engaged research
  • Experience coordinating multi-site, federally funded, or clinic-based research studies
  • Familiarity with community-based participatory research (CBPR) or stakeholder-engaged research approaches
  • Experience working in a community health center, FQHC, or safety-net clinical setting
  • Clinical research certification such as SOCRA or ACRP, or willingness to obtain certification

Benefits

  • Medical/Dental/Vision
  • 401(k)/Roth plan with matching
  • Healthcare Savings Accounts
  • Ongoing training throughout your employment
  • Paid Time Off and Holidays throughout the year to recharge
  • Company sponsored Whole Health programs designed to recharge our teams

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