Job... 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...
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 are looking for experienced Clinical Project Managers (CPM) to join our Real-World Evidence (RWE) Project Management group - a fast paced, dynamic and customer focused team.
You will have a strong background (c3 years for CPM and c5 years for Senior CPM) in Late Phase prospective and retrospective activity including Non-Interventional/Observational Studies in the CRO/pharmaceutical industry. You will also need prior Project Management experience.
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.
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 defence preparations, and, in the Senior CPM role, 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, depending on the level of the role may include:
Everyone in the RWE CPM function has previous experience managing international clinical studies in the CRO/pharmaceutical industry. We also require our team to have previously been involved in late-phase trials.
For both roles you’ll also need:
And in addition for the Senior CPM role:
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.
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.
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