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IQVIA

Runs drug trials and sells health data to pharma

Freelance Clinical Research Associate

Clinical Research OperationsConfirmed live in the last 24 hours
Part-timeNo salary listed

About the Job

Requirements

  • At least 2 years of independent Clinical Research Associate monitoring experience.
  • Previous Phase III clinical trial experience.
  • Strong knowledge of International Council for Harmonisation Good Clinical Practice (ICH-GCP) and clinical trial processes.
  • Ability to work independently and manage assigned sites.
  • Fluency in Spanish and English.
  • Willingness and ability to travel to assigned sites within Spain.

Responsibilities

  • Perform Interim Monitoring Visits and other required site monitoring activities.
  • Ensure protocol adherence and International Council for Harmonisation Good Clinical Practice compliance.
  • Review source documentation and study data.
  • Support investigators and site personnel.
  • Identify and follow up on site issues and action plans.
  • Work closely with project and study teams to ensure high-quality study delivery.

Desired Qualifications

  • Hands-on oncology experience would be an advantage.

About the Company

IQVIA

Runs drug trials and sells health data to pharma

IQVIA runs clinical trials for drug, biotech and medical device companies and sells them the health data, software and analytics they use to develop and market treatments. Its research arm designs studies, recruits trial sites and patients, and manages trials through to regulatory filing. Its commercial arm sells market data, consulting and software that pharma sales and marketing teams use to plan product launches. Clients pay through multi-year service contracts and data and software subscriptions. IQVIA was formed in 2016 when clinical research firm Quintiles merged with health data company IMS Health, and it is based in Durham, North Carolina.

Company size
10,001+
Company stage
IPO
Headquarters
Durham, NC
Founded
1998

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