IQVIA

healthcare

ClinicalResearchCoordinator

$0–0k Philadelphia, Pennsylvania, United States PART TIME Remote Friendly
The Brief

“Clinical Research Coordinator at IQVIA. Skills: Clinical Research Coordination, Patient Care, Data Management, Regulatory Compliance. Perform clinical procedures such as ECGs, vital signs, and biological sample collection in accordance with study protocols. Coordinate day-to-day clinical trial activities while ensuring compliance with GCP, protocol, and regulatory requirements”

What You'll Achieve.

ensure studies are conducted safely, efficiently, and in compliance with regulatory standards; maintain high data quality standards

Industry & Context.

healthcare
Problems you'll solve

Resolve data queries in a timely manner

Eligibility Requirements

not eligible for visa sponsorship

What They're Looking For.

Must Have

Minimum of 1 + years of clinical research experience in a coordinator or similar role, Working knowledge of clinical trial processes, GCP guidelines, medical terminology, Proven ability to conduct patient study visits in accordance with protocol requirements, Experience in patient recruitment, including chart review and phone screenings, Proficiency with EDC systems, including accurate data entry and query resolution

Nice to Have

Bachelor’s degree, Cardiovascular research experience

What You'll Do.

Perform clinical procedures such as ECGs

and biological sample collection in accordance with study protocols

Coordinate day-to-day clinical trial activities while ensuring compliance with GCP

and regulatory requirements

Prepare study materials

and support overall site readiness

Conduct patient recruitment activities

including chart review

and scheduling study visits

Perform and manage patient study visits in accordance with protocol requirements

Educate and orient participants

ensuring a high standard of patient care and safety

and enter data into EDC systems and case report forms (CRFs)

Resolve data queries in a timely manner and maintain high data quality standards

Collaborate with investigators

and monitors during site visits and audits

Serve as a patient advocate and maintain a safe

compliant clinical environment

How You'll Work.

Team & Collaboration

Collaborate with investigators, sponsors, and monitors during site visits and audits; ability to build collaborative working relationships

Communication Scope

Effective communication skills

Process & Methodology

ability to manage multiple priorities

Free ATS check

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