Associate Clinical Project Manager (R1089353) - Overland Park, KS - IQVIA™

Date de publication 9/5/2019

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.


Assist in the execution of the assigned regionally-based clinical study(ies) per Contract, from initiation through to

closeout. Support all clinical study related activities for assigned projects in accordance with SOPs, policies and

practices, meeting quality and timeline metrics.


Create, track and report on project timelines.

Produce and distribute status, tracking and financial reports for internal and external team members and senior


Assist the clinical project manager(s) with budget allocation and approval of invoices.

Serve as primary back up project contact with Sponsor and internal project team to ensure communication is

maintained and reporting schedules are adhered to.

Identify out of scope project work. Escalate findings and action plans to appropriate parties.

Coordinate data gathering for the development of proposals for new work.

Prepare and present project information at internal and external meetings.

Coordinate with other project support staff within and outside the Clinical Project Management Unit to identify

and consolidate support processes.

Undertake clinical project management activities as directed by Clinical Project Manager.

Train and may coordinate the work of more junior project support staff.

May provide direct site support (on site visits)


Understanding of applicable clinical research regulatory requirements; i.e., Good Clinical Practice (GCP) and

International Conference on Harmonisation (ICH) guidelines

Basic therapeutic and protocol knowledge

Strong communication and interpersonal skills, including good command of English language

Good problem solving skills

Demonstrated ability to deliver results to the appropriate quality and timeline metrics

Good teamwork skills

Excellent customer service skills

Ability to work under limited direction

Strong software and computer skills, including MS Office applications

Ability to establish and maintain effective working relationships with coworkers, managers and clients


Bachelor's degree in life sciences or related field and 3 years’ clinical research experience; or equivalent

combination of education, training and experience.


Extensive use of keyboard requiring repetitive motion of fingers.

Extensive use of telephone and face-to-face communication requiring accurate perception of speech.

Regular sitting for extended periods of time.

May require occasional travel.

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.

IQVIA is an EEO Employer - Minorities/Females/Protected Veterans/Disabled

IQVIA, Inc. provides reasonable accommodations for applicants with disabilities.  Applicants who require reasonable accommodation to submit an application for employment or otherwise participate in the application process should contact IQVIA’s Talent Acquisition team at to arrange for such an accommodation.

Job ID: R1089353