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IQVIA

Runs drug trials and sells health data to pharma

Safety Associate

Regulatory & Quality (Life Sciences)Posted on Nov 13
Full-timeDalian, Liaoning, ChinaNo salary listed

About the Job

Requirements

  • A high school diploma or equivalent in a scientific or healthcare discipline or allied life sciences is required.
  • A bachelor's degree in a scientific or healthcare discipline or allied life sciences, plus 1–1.5 years of relevant experience, is required.
  • Knowledge of medical terminology is required.
  • Working knowledge of the applicable safety database is required.
  • Knowledge of applicable global, regional, and local clinical research regulatory requirements is required.
  • Attention to detail and accuracy are required.
  • Working knowledge of Microsoft Office and web-based applications is required.
  • Organizational and time-management skills are required.
  • Verbal and written communication skills are required.
  • Self-motivation and flexibility are required.
  • Ability to follow instructions and guidelines, use initiative, and work independently is required.
  • Ability to multitask and manage competing priorities and deadlines is required.
  • Ability to delegate to less experienced team members is required.
  • Willingness and aptitude to learn new skills across safety service lines is required.
  • Ability to establish and maintain effective working relationships with coworkers, managers, and clients is required.
  • Ability to contribute as a team member toward team goals is required.
  • Ability to ensure deliverables meet agreed quality terms is required.
  • Ability to demonstrate IQVIA core values in daily tasks is required.
  • Ability to accurately perceive speech during extensive telephone and face-to-face communication is required.
  • Ability to sit regularly for extended periods is required.
  • Flexibility to work shifts is required.

Responsibilities

  • Prioritize and complete assigned training on time.
  • Process safety data according to applicable regulations, guidelines, standard operating procedures, and project requirements.
  • Perform project-specific pharmacovigilance activities, including collecting and tracking incoming adverse events and endpoint information.
  • Determine the initial or updated status of incoming events.
  • Enter data into databases.
  • Code adverse events and products, write narratives, and perform literature-related activities within internal and project timelines.
  • Meet project quality standards.
  • Meet project productivity and delivery standards.
  • Ensure compliance with all project-related processes and activities.
  • Create, maintain, and track cases as applicable to the project plan.
  • Identify quality problems and bring them to the attention of a senior team member.
  • Apply problem-solving capabilities.
  • Mentor new team members when assigned by the manager.
  • Attend project team meetings and provide the operations manager with feedback on challenges, issues, and successes.
  • Comply with people practices and processes.
  • Perform other duties as assigned.

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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