Opportunities at IQVIA

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 defence preparations, and, in the Senior Clinical Project Manager 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:

• 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
• Support 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

Candidate Requirements:

• You must have previous experience managing international clinical studies in Late Phase prospective and retrospective activity including Non-Interventional/Observational Studies in the CRO/pharmaceutical industry.

For both roles you’ll also need:

• Strong collaboration and influencing skills, with experience of managing cross-functional project teams
• Proven ability to work independently in a complex matrix environment
• Thorough knowledge of GCP and global clinical development processes
• Demonstrable presentation, diplomacy, negotiation and conflict resolution skills
• A strong customer-oriented mindset
• Already possess the right to work in the hiring country without the need of a visa/sponsorship

And in addition for the Senior CPM role:

• Bid defense experience
• 2 further years experience as detailed above
• Study budget management experience
• Proven ability to coach and mentor

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Job Overview

Data Strategists will be vital function in the evolution of data collection and overall operational delivery models for IQVIA RWS. This role will work with the leadership team in the Data Strategy, Access and Enablement group as we develop innovative data collection delivery models and technology assets. This role will operate as a strategy leader and change agent to transfer and embed these capabilities and knowledge within the IQVIA RWS delivery organisation. This role will also operate alongside Evidence Strategy and Data Management teams to support GTM pursuits and the deployment of novel data collection methodologies within projects

Essential Functions

• Lead operational insights and collaboration with GTM stakeholders to ensure the selection and deployment of optimal data collection platforms to support new opportunities, including:
• Participation in Delivery Strategy Review alongside the RWE leadership team to evaluate the application of novel data collection approaches for new business opportunities.
• Lead strategic insights into the application of novel data collection strategies for new opportunities, including collaboration with Evidence Strategy Leads and Data Team Leads on the following specific tasks:
• Patient Journey and Data Journey mapping.
• Identification of novel technologies for data collection, including application of Data Enabled collection, Decentralised or Direct to Patient modalities.
• Provide recommendation to Evidence Strategy Leads on the optimal mix of novel data collection technologies.
• Support GTM organisation in requirements setting related to pricing for novel data collection technologies.
• Attend Bid Defence Meetings as a subject matter expert in the application of novel data collection technologies.
• Provide delivery leadership in the implementation of novel data collection technologies, including collaboration with Evidence Strategy Leads and Data Team Leads on the following specific tasks:
• Support definition of project level data source and data flow mapping.
• Support review of data interoperability and integration requirements for novel data collection methodologies.
• Support Data Risk Planning and Data Privacy Review on projects
• Support integration and deployment of novel data collection methodologies
• Support Change in Scope Management related to deployment of novel data collection methodologies.
• Operate as a change agent for RWS organisation including, participation in the development of collaboration, training and implementation models for embedding knowledge of novel data collection methodologies into functional teams with RWE.
• Support Head of Emerging Design Delivery in specific knowledge management and transfer projects to help the RWE organisation embed novel data collection into operational delivery.

Minimum Experience Requirements over and above total years of CRO experience required for job grade:

• Minimum of 6 years experience in a function such as Data Management, Epidemiology, Data Generation/Site Management, Project Management, Real World Data roles.
• Demonstrate experience of supporting solutioning or consulting engagement with biopharma clients in for real world research projects (including prospective and retrospective research using primary or secondary data sources)
• Demonstrate experience of the set-up of real world research projects both primary and secondary data collection
• Demonstrate knowledge and understanding of decentralised and direct to patient data collection
• Demonstrate knowledge and understanding of patient and site mediated EMR use in real world research
• Demonstrate knowledge and understanding of data collection, data privacy and data quality dynamics in real world research