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Senior Clinical Project Manager/Clinical Project Manager, Real World Evidence (Home-Based, flexible across Europe)(m/w/d)

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Primary Location: Reading, Berkshire, United Kingdom Additonal Locations: Barcelona, Spain,ESP; Bratislava, Slovakia,SVK; Budapest, Hungary,HUN; Dublin, Ireland,IRL; Espoo, Finland,FIN; Frankfurt, Germany,DEU; London, United Kingdom,GBR; Madrid, Spain,ESP; Oslo, Norway,NOR; Paris, France,FRA; Rome, Italy,ITA; Sofia, Bulgaria,BGR; Vienna, Austria,AUT; Warsaw, Poland,POL; Zagreb, Croatia,HRV Full time R1307451

Job description

We are looking Senior/Clinical Project Manager’s to join our innovative and dynamic Real-World Evidence (RWE) Project Management Group of global professionals dedicated to assisting our clients in driving healthcare forward. This is an important and high-profile role within our Real-World Solutions business unit, to enable medical breakthroughs that advance healthcare and patient treatment options around the world. To be considered you must possess a strong record of delivery as a Clinical Project Manager in Late Phase prospective and retrospective activity including Non-Interventional/Observational Studies in the CRO/pharmaceutical industry.

IQVIA™ Real-World Evidence (RWE) teams work with clients to help them collect and use real-world data to generate evidence to meet the needs of regulators, payers, providers, and patients. Our approach is unique in the industry and is defining the way companies can develop and apply real-world evidence to provide deeper insight about market dynamics, therapy area changes, outcomes research and other scientific insights.

What makes the Real-World Project Management team different?

Unlike most other large CROs, our PMs are trained specialists dedicated to Real World Studies, translate innovative solutions complex leading-edge technologies into operational reality for customers and apply processes and procedures specifically designed for the Real-World Studies. In return the size and scope of IQVIA™ will allow you to experience rapid personal development across global studies enjoying a varied, busy, and sometimes demanding schedule.  You’ll also have dedicated support to develop your IQVIA career.

Main responsibilities:

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

  • You’ll participate in bid defense preparations, and, in the Senior Clinical Project Manager role, will have the opportunity to lead bid defense 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.

  • Managing and coordinating 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.

  • 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.

Required Knowledge, skills and abilities:

  • Bachelor's degree in life sciences or related field.

  • Minimum of 2 years’ experience (+5 for the Senior CPM role) managing international clinical studies in Late Phase/ IV phase prospective and retrospective activity including Non-Interventional/Observational Studies in the CRO industry.

  • Thorough knowledge of GCP and global clinical development processes.

  • Strong collaboration and influencing skills, with experience of managing cross-functional project teams and a strong customer-oriented mindset.

  • Demonstrable presentation, diplomacy, negotiation, and conflict resolution skills.

In addition, for the Senior CPM role, you must have bid defense and study management experience as well as proven ability to coach and mentor.

IQVIA is a leading global provider of advanced analytics, technology solutions and clinical research services to the life sciences industry. We believe in pushing the boundaries of human science and data science to make the biggest impact possible – to help our customers create a healthier world. Learn more at https://jobs.iqvia.com

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