Sr Clinical Project Manager (R1013988) in Hoofddorp, NL at IQVIA™

Date Posted: 7/13/2018

Job Snapshot

  • Employee Type:
    Full-Time
  • Location:
    Hoofddorp, NL
  • Experience:
    Not Specified
  • Date Posted:
    7/13/2018
  • Job ID:
    R1013988

Job Description

Global Clinical Project Manager

Late Phase and Real World Evidence

Office or homebased contracts possible across Europe


IQVIA are looking for experienced Clinical Project Managers to join our Real World Evidence Project Management group -  a fast paced, dynamic and customer focused team.


The size and scope of IQVIA™ will allow you to develop and experience rapid growth across global studies, and you will be working on several projects at the same time, enjoying a varied and busy, sometimes demanding, schedule.  At the same time you’ll have dedicated support to develop your career.


Through your management of clinical project teams, you’ll be responsible for clinical study and project productivity, delivery and quality, resulting in strong financial performance and most importantly, customer satisfaction.


You’ll participate in bid defence preparations, and will have the opportunity to lead bid defence presentations in partnership with our Business Development teams for multi-country/ region studies.  You’ll also be involved in developing the delivery strategy for RFP’s.


Other responsibilities could include:

  • Managing and co-ordinating efforts of cross-functional project teams to support milestone achievement and to manage study issues and obstacles. Implementing continuous improvement activities for assigned projects.
  • Serving as primary project contact with Sponsor to ensure communication is maintained and continuously improved and reporting schedules are adhered to.
  • Reporting on team performance against contract, customer expectations, and project baselines to management.
  • Leading problem solving and resolution efforts to include management of risk, contingencies and issues. Developing proactive contingency plans to mitigate clinical risk.
  • Providing input to line managers of their project team members' performance relative to project tasks, and supporting staff development. Mentor less experienced CPMs.
  • Ensure high performance and efficiency of the clinical team through the scheduling of co-monitoring/accompanied site visits and ongoing mentoring of CRA team.
  • Prepare and present project information at internal and external meetings.

Everyone in the RWE Clinical Project Management function has previous relevant experience in a clinical development organization, managing global clinical studies in the CRO/pharmaceutical industry.  We also require our team to have previously been involved in late-phase, global trials.


You’ll also need:

  • Strong leadership and management skills, with experience of managing cross-functional project teams
  • Proven ability to work independently in a complex matrix environment
  • Thorough knowledge of Good Clinical Practice, and global clinical development processes.
  • Demonstrated presentation and diplomacy skills. Negotiation and conflict resolution skills.
  • A strong customer-oriented mindset
  • Bid Defence experience

Next steps:

You will be contacted by one of our recruiters to arrange a prescreen call should your background be relevant for this opportunity who will be able to give you more information on this team and the opportunity and also explain the assessment process to you for this role.



Job ID: R1013988