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IQVIA

Runs drug trials and sells health data to pharma

Lab Project Coordinator

Clinical Research OperationsConfirmed live in the last 24 hours
Full-timeBeijing, ChinaNo salary listedIn-person

About the Job

Requirements

  • High school diploma or equivalent is required.
  • At least 1 year of relevant experience is preferred; clinical, medical, or healthcare industry experience is preferred.
  • An equivalent combination of education, training, and experience may be considered.
  • Strong interpersonal, communication, organizational, and time management skills are required.
  • Ability to comply with all applicable company standards is required.
  • Ability to handle multiple competing priorities and use resources effectively is required.
  • Critical thinking and problem-solving ability is required.
  • Strong written and verbal communication skills, including a good command of English, are required.
  • In geographies where local-language communication is desired, excellent command of the local language with reasonable English proficiency is preferred.
  • Computer proficiency in word processing, presentation, and spreadsheet applications is required.
  • Ability to establish and maintain effective working relationships with coworkers and managers is required.

Responsibilities

  • Support the Project Manager and related team members with routine procedures and tasks for day-to-day project operations throughout the study lifecycle, including start-up, maintenance, and close-out.
  • Ensure work is conducted in line with standard operating procedures, policies, and good practices.
  • Support the Project Manager by attending meetings, preparing minutes and action logs, and preparing protocol-specific laboratory instruction documents.
  • Under the Project Manager's supervision, oversee setup of protocol-specific Laboratory Centralized Monitoring requirements.
  • Perform routine tasks across assigned studies, including site loading, Investigator Portal access, kit shipments, monitoring day-to-day study performance, and overseeing Laboratory Centralized Monitoring.
  • Work with internal and external teams to manage timely resolution of queries, protocol questions, issues, and escalations.
  • Use status reports, monitoring tools, and outputs to proactively identify trends and provide feedback to internal and external teams on Investigator site and company-service performance.
  • Support the Project Manager with administrative study tasks.
  • Coordinate and communicate with relevant stakeholders, including leading customer communications and activities when the Project Manager is absent.
  • Oversee project close-out.
  • Represent the company at internal and external meetings as needed and participate in external and internal audits and inspections.
  • Support study training with sites, CRAs, and customers as required.
  • Ensure outputs meet organizational standards, protocol-specific requirements, and customer expectations.

Desired Qualifications

  • A Bachelor's degree in Life Sciences or a related field is preferred.
  • Ability to work in a fast-paced environment is highly desirable.

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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