IQVIA

Healthcare

ClinicalResearchCoordinator

$0–0k New York, New York, United States PART TIME Remote Friendly
The Brief

“Clinical Research Coordinator at IQVIA. Skills: Clinical Research Coordinator, patient-facing, manage multiple protocols, patient safety, regulatory compliance, data integrity, study activities, coordinating visits, regulatory requirements. Conduct clinical research visits and procedures, including ECGs, vital signs, and biological sample collection. Coordinate day-to-day execution of multiple clinical research protocols simultaneously”

What You'll Achieve.

improve patient outcomes

Industry & Context.

Healthcare
Problems you'll solve

query resolution

Eligibility Requirements

This position is not eligible for sponsorship

What They're Looking For.

Must Have

Minimum of 1+ years of clinical research experience, working knowledge of clinical trial operations, GCP, and medical terminology, Proficiency in EDC systems, data entry, and query resolution, High attention to detail, Ability to build effective working relationships across cross-functional teams

Nice to Have

Bachelor’s degree preferred or an equivalent combination of education and relevant experience, Significant experience as a Clinical Research Coordinator, including prior responsibility as a Lead CRC managing multiple protocols concurrently, Demonstrated experience conducting study visits independently and providing regulatory support, Experience in Neurology and/or Pediatrics is a plus

What You'll Do.

Conduct clinical research visits and procedures

and biological sample collection

Coordinate day-to-day execution of multiple clinical research protocols simultaneously

Ensure strict adherence to study protocols

Good Clinical Practice (GCP)

and applicable regulatory requirements

Prepare study materials

and manage logistical planning for study visits

and orient study participants while ensuring safety and ethical conduct

Accurately document clinical data in case report forms (CRFs) and electronic data capture (EDC) systems

Provide regulatory support

including maintenance of essential documents and audit readiness

Serve as a patient advocate and maintain a safe clinical environment in accordance with Health & Safety policies

How You'll Work.

Team & Collaboration

Collaborate with investigators, monitors, and sponsors to resolve queries and maintain data quality; build effective working relationships across cross-functional teams

Process & Methodology

manage multiple protocols concurrently

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