Director, Clinical Data Management- Real World Evidence (R1013647) in Cambridge, MA at IQVIA™

Date Posted: 9/12/2018

Job Snapshot

  • Employee Type:
    Full-Time
  • Location:
    Cambridge, MA
  • Job Type:
  • Experience:
    Not Specified
  • Date Posted:
    9/12/2018
  • Job ID:
    R1013647

Job Description

Director of Data Management

Flexible locations across EMEA – home or office based.


We have an exciting opportunity for a Director to take a leadership role within our Real World Evidence Data Management unit.


Within IQVIA, our Real-World & Analytics Solutions (RWAS) business unit employs over 1,000 people, designing, implementing and managing real-world and post-marketing studies. As healthcare stakeholders increasingly need evidence to support regulatory, reimbursement and prescribing decisions, the IQVIA RWES team offers a comprehensive evidence approach to meet our customer’s unique needs for demonstrating safety, effectiveness and quality.  


The Director, Clinical Data Management, leads the Data Management team to efficiently produce databases that meet our clients requirements.  In this role, you’ll be responsible for all project resourcing, and the utilisation of the team, as well as monitoring and managing productivity. We’ll also look to you to define strategies for new processes and technology at either regional or global levels, and identify trends and opportunities for improvements


Other responsibilities include:


  • Defining and implementing department objectives
  • Monitoring quality and efficiency across projects
  • Performance Management – responsible for hiring, training and ongoing appraisal and development of team members
  • Providing operational input into proposals for large programs and strategic partnerships, including input to costing
  • algorithms and standard proposal text.
  • Attend client meetings and lead discussions of project requirements and strategic planning.

To be successful in this role you’ll need advanced knowledge of Data Management processes and systems including new technologies, and proven leadership skills within a data management function, ideally gained within a CRO/ pharma environment.  Significant experience of global drug development is a must.


You’ll also need:

  • Outstanding written and oral communication skills
  • Excellent organizational skills and demonstrated ability to delegate and monitor quality of outputs
  • Ability to establish and maintain effective working relationships with coworkers, managers and clients.

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: R1013647