CRA Phase IV/NIS projects (R1122915) in Warsaw, PL at IQVIA™

Date Posted: 3/12/2020

Job Snapshot

  • Employee Type:
    Full-Time
  • Location:
    Warsaw, PL
  • Experience:
    Not Specified
  • Date Posted:
    3/12/2020
  • Job ID:
    R1122915

Job Description

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.

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.

We are offering an exciting job opportunity as Late Phase CRA  to work mainly in the field of Phase IV / Non-Interventional Studies and to join IQVIA. 

While projects vary, your typical responsibilities might include:

  • Performing site selection, initiation, monitoring and close-out visits, plus maintaining appropriate documentation for Phase IV/NIS projects
  • Supporting the development of a subject recruitment plan
  • Establishing regular lines of communication plus administering protocol and related study training to assigned sites
  • Evaluating the quality and integrity of site practices – escalating quality issues as appropriate
  • Managing progress by tracking regulatory submissions, recruitment, case report form (CRF) completion, and data query resolution
  • Taking part in the study start-up process - contracts management, EC, CA submissions
  • Covering sites in Poland (1 monitoring visit per week)

You should have:

  • A Bachelor's degree in a health care or other scientific discipline or educational equivalent
  • At least two years of on-site monitoring experience
  • Alternatively, you should have an equivalent combination of education, training and experience
  • Fluent English language skills
  • Experience in Phase IV/NIS or in contracts management and EC/CA submissions would be beneficial
  • You will need to be comfortable collaborating and communicating with a variety of colleagues and customers. Ideally, you will also have a good basic knowledge of applicable clinical research regulatory requirements.

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.

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: R1122915