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IQVIA

Runs drug trials and sells health data to pharma

Senior Laboratory Project Services Coordinator

Clinical Research OperationsConfirmed live in the last 24 hours
Full-timeSingaporeNo salary listedIn-person

About the Job

Requirements

  • A bachelor's degree in life sciences or a related field, or an equivalent combination of education, training, and experience.
  • One to three years of relevant experience; experience in the clinical, medical, or healthcare industry is preferred.
  • Strong interpersonal, communication, organizational, and time management skills.
  • Ability to handle multiple competing priorities and apply critical thinking and problem-solving.
  • Strong written and verbal communication skills, including a good command of English.
  • In geographies where local-language communication is desired, excellent command of the local language with reasonable proficiency in English is preferred.
  • Computer proficiency in word processing, presentation, and spreadsheet applications.
  • Ability to establish and maintain effective working relationships with coworkers and managers.
  • Proficiency in Mandarin due to the nature of the global portfolio.

Responsibilities

  • Support the Project Manager by attending meetings, preparing minutes and action logs, and preparing protocol-specific laboratory instruction documents.
  • Under 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.
  • Provide input into monitoring plans, reports, and protocol-specific materials; assist with document quality-control reviews; and, where required, oversee and monitor Sample Management activity.
  • Coordinate and communicate with relevant stakeholders, including leading customer communications and activities as needed.
  • Represent the company at internal and external meetings and participate in external and internal audits or inspections as required.
  • Support study training with sites, CRAs, and customers, including representing the company at Investigator or client meetings.
  • Conduct project launch meetings or other meetings on behalf of the Project Manager as needed.
  • Develop and present information to internal and external audiences.
  • Mentor and assist in training junior staff.
  • Provide input into internal process-improvement projects and SOP revisions.
  • Ensure outputs are delivered in line with organizational standards, protocol-specific requirements, and customer expectations.

Desired Qualifications

  • Experience in the clinical, medical, or healthcare industry is preferred.
  • Ability to work in a fast-paced, high-stress environment is highly desirable.
  • In geographies where local-language communication is desired, excellent command of the local language with reasonable proficiency in English is preferred.

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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