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Job Description

Study Coordinator - virtual

Warsaw, Poland Part time R1458224

Warsaw, Poland

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Job Description

Study Coordinator - Virtual

Are you ready to join an industry-leading company? IQVIA is seeking a remote Decentralized Trials Study Coordinator to support clinical research sites across various countries.

Position Details:

Type: Part-time (around 20 hours per week)

Location: Remote in Poland

Start: in January/February 2025

Duration of contract: one year

Key Responsibilities:

  • Collect, record, report, and interpret data on patients enrolled or seeking enrollment in clinical studies.
  • Provide clinical research support to investigators for the preparation and execution of assigned research studies.
  • Review and understand study protocols, Case Report Forms (CRFs), and other study-specific documents.
  • Utilize electronic data capture systems to record clinical research data.
  • Schedule and coordinate remote visits, and support actual remote visits with the Principal Investigator (PI).
  • Train new investigator site staff on study-specific topics and requirements.
  • Audit and maintain training records to ensure adherence to investigator site staff training requirements.
  • Prepare for and remotely attend study monitoring visits, audits, and regulatory inspections.
  • Communicate with patients and team members via telephone, teleconference, email, and chat.
  • Support study participants with pre-screening, consent, and virtual visit activities.
  • Coordinate with home health services and participants during the study.
  • Orient research subjects to the study, including explaining the purpose, procedures, and protocol timelines.
  • Collect and submit regulatory/ethics documentation as required by the FDA and other regulatory bodies.

Qualifications:

  • BS/BA in life sciences or equivalent education and/or relevant work experience in a clinical study environment (e.g., clinical research coordinator, research assistant, study nurse, clinical trial educator).
  • Strong knowledge of clinical trials and in-depth understanding of departmental, protocol, and study-specific operating procedures.
  • Basic knowledge of medical terminology.
  • Proficiency in MS Windows and Office applications (Access, Outlook, Excel, Word).
  • Excellent interpersonal skills with the ability to establish and maintain effective working relationships.
  • Strong organizational skills with attention to detail.
  • Willing and capable of working remotely
  • Fluent in Polish and English; additional languages are a plus.

If this sounds like the perfect opportunity for you, apply now!

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IQVIA is a leading global provider of clinical research services, commercial insights and healthcare intelligence to the life sciences and healthcare industries. We create intelligent connections to accelerate the development and commercialization of innovative medical treatments to help improve patient outcomes and population health worldwide. Learn more at https://jobs.iqvia.com

Apply Now

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