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NIVA Health

Clinical Research Study Coordinator (Remote)

1w

NIVA Health

ZA · Full-time · $1,600 – $1,600/mo

About this role

NIVA Health invites meticulous professionals passionate about advancing patient care through research in clinical trial coordination, regulatory compliance, and patient management, especially in wound care. As a key member of the research coordination team, you will ensure patients access innovative therapies. Exemplify Core Values of Teamwork, Resilience, Open-Mindedness, Ownership, and Positivity every day.

Coordinate all aspects of assigned clinical studies related to advanced wound care and skin substitute therapies. Screen, recruit, and consent eligible patients per study protocols, while scheduling visits and performing clinical assessments within RN scope. Maintain thorough documentation of wound characteristics and treatment response, monitoring patient safety and adverse events.

Serve as primary liaison between investigators, sponsors, CROs, and clinical teams in a nationwide team delivering compassionate care. Uphold compliance with FDA, IRB, GCP, and sponsor requirements through regulatory binders and EDC data entry. Provide regular study updates to leadership and participate in training sessions.

Your dedication at NIVA Health ensures patients benefit from cutting-edge therapies and world-class care. The values-driven, supportive environment celebrates achievements and invests in personal and professional growth. Join to shape a brighter, healthier future one successful study at a time.

Requirements

  • Possess an active Registered Nurse (RN) license in good standing
  • Have experience coordinating or supporting clinical trials
  • Demonstrate strong knowledge of clinical research processes and regulatory standards (GCP)
  • Highly detail-oriented, organized, and have excellent written/verbal communication skills
  • Adept with data entry and electronic data capture systems
  • Can manage multiple studies and timelines independently while contributing to a collaborative team

Responsibilities

  • Coordinate all aspects of assigned clinical studies related to advanced wound care and skin substitute therapies
  • Screen, recruit, and consent eligible patients in accordance with study protocols
  • Schedule and conduct study visits; perform clinical assessments within RN scope of practice
  • Ensure thorough, accurate documentation of wound characteristics and treatment response
  • Monitor patient safety and report adverse events in line with regulatory standards
  • Maintain compliance with FDA, IRB, GCP, and sponsor requirements
  • Enter and track accurate study data in electronic data capture (EDC) systems
  • Serve as the primary liaison between investigators, sponsors, CROs, and clinical teams

Benefits

  • Values-driven, supportive environment
  • Investment in personal and professional growth
  • Meaningful work advancing patient access to innovative therapies
  • Remote work in US East Coast timezone