Lab Project Services/Set-up Coordinator (R1086298) en Singapore, SG de IQVIA™

Fecha de publicación 9/1/2019

Resumen de la oferta

  • Tipo de empleado:
    Tiempo completo
  • Ubicación:
    Singapore, SG
  • Experiencia:
    Not Specified
  • Fecha de publicación
  • ID del Empleo:

Descripción del trabajo

IQVIA™ is the leading human data science company focused on helping healthcare clients find unparalleled insights and better solutions for patients. Formed through the merger of IMS Health and Quintiles, IQVIA offers a broad range of solutions that harness the power of healthcare data, domain expertise, transformative technology, and advanced analytics to drive healthcare forward.


Provide pre-launch database support; assist with designing, loading, and validation of Lab databases using Clinical Trials Management System [examples QLIMs, NewLIMs, TOPCAT, Encompass]; ensure work is conducted in line with standard operating procedures, policies and good practice.


  • Configure project databases.
  • Input data into the databases adhering to design specifications.
  • Support online protocols and amendments.
  • Perform a database configuration review and assist with validation of database specifications.
  • Research problems, gather information, and liaise with lab colleagues to help ensure projects are set-up in line with established procedures and customer requirements.
  • Maintain project documentation files.
  • Keep Project Managers and other relevant staff informed of any issues that may affect the smooth running of the project.
  • Coordinate meetings with relevant colleagues and internal departments (e.g. planning and handover meetings).
  • Develop solutions for routine project related issues and problems, within a limited scope.
  • Participate in local and global improvement projects as defined by the relevant process improvement management team.
  • Participate in internal audits, as required.
  • May have occasional, limited contact with study Sponsor(s) (e.g. exchanging factual information).

Ideal candidates should possess the following:

  • Bachelor’s Degree in Biomedical Science or related
  • At least 1 year of related experience in clinical research/trials, either as a Clinical Research Coordinator OR Clinical Monitor. Fresh graduates are also considered for this level of hire.
  • Possess strong interpersonal skills
  • Demonstrated ability to meet deadlines.
  • Demonstrated computer proficiency with Microsoft Office
  • Working knowledge of Clinical Trials Management Systems would be an advantage [examples QLIMs, NewLIMs TOPCAT, Encompass].
  • Possess an understanding of medical and clinical research terminology.
  • Demonstrated ability to work in a fast-paced, high stress environment.
  • Knowledge of Project Management processes and terminology.
  • Excellent organizational and time management skills
  • Excellent accuracy and attention to detail skills
  • Strong written and verbal communication skills written & spoken, influencing & negotiating

Join Us

Making a positive impact on human health takes insight, curiosity, and intellectual courage. It takes brave minds, pushing the boundaries to transform healthcare. Regardless of your role, you will have the opportunity to play an important part in helping our clients drive healthcare forward and ultimately improve outcomes for patients.

Forge a career with greater purpose, make an impact, and never stop learning.

Job ID: R1086298