Clin Project Mgr (Late Phase focused) (R1106541) - Seoul,SK - IQVIA™

Date de publication 2/20/2020

Résumé de l'offre

  • Type d'employé
    CDI / CNE
  • Expérience
    Not Specified
  • Date de publication
  • Job ID:

Description de l'offre

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.

Essential Functions

  • Manage and co-ordinate efforts of cross-functional project teams to support milestone achievement and to manage study issues and obstacles to ensure consistent use of study tools and training materials and compliance with standard processes, policies, and procedures.
  • Develop study management plans, together with team assignments and accountabilities and oversight of database maintenance.
  • Serve as primary project contract with Sponsor to ensure communication is maintained and reporting schedules are adhered to
  • Collect information on team performance against contract, customer expectations, and project baselines
  • Lead problem solving and resolution efforts to include management of risk, contingencies, and issues
  • Identify quality issues within the study to implement appropriate corrective action plans.  Escalate findings and action plans to appropriate parties.
  • Provide input to line managers of their project team members performance relative to project tasks
  • Prepare and present project information at internal and external meetings
  • Participate in proposal development and in the bid-defense process with guidance and supervision
  • Ensure high performance and efficiency of the clinical team through the scheduling of co-monitoring/accompanied site visits and ongoing mentoring of the CRA team


To perform this job successfully, an individual must be able to perform each essential duty satisfactorily. The requirements listed below are representative of the knowledge, skill, and/or ability required. Reasonable accommodations may be made to enable individuals with disabilities to perform the essential functions.


  • Typically requires 3 - 5 years of prior relevant experience.


  • Requires advanced knowledge of job area, and broad knowledge of a other related job areas, typically obtained through advanced education combined with experience.
  • Education Level : Bachelor's Degree
  • Life sciences or related field

Additional Work Experience

  • 5 years clinical research experience including 2 years project management experience
  • Equivalent combination of education, training and experience

Skills and Abilities

  • In depth knowledge of, and skill in applying, applicable clinical research regulatory requirements; i.e., Good Clinical Practice (GCP) and International Conference on Harmonization (ICH) guidelines
  • Good therapeutic and protocol knowledge
  • Strong communication and interpersonal skills, including goog command of English language
  • Good problem solving skills
  • Demonstrated ability to deliver results to the appropriate quality and timeline metric
  • Excellent customer service skills
  • Good presentation skills
  • Good judgement
  • Strong software and computer skills, including MS office applications
  • Ability to establish and maintain effective working relationships with coworkers, managers, and clients

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: R1106541