We are currently looking to recruit experienced Clinical Project Manager to be based within our ANZ Project Leadership Team. This is a fantastic opportunity for someone with strong leadership capabilities, a track record in managing customer expectations, exceptional communication and stakeholder management skills and motivation to succeed, who is looking to move into a Project Leadership role within IQVIA.
As a CPM , you will manage the execution of the assigned clinical study(ies) per contract, from initiation through to closeout. You will ensure that all project deliverables under your remit are completed to the customer’s satisfaction, ensuring quality deliverables on time and within budget and in accordance with SOPs, policies and practices.
+ Contributing to the development of the project delivery strategy for RFPs. Participate in bid defence preparations. Understand project strategy and translate the agreed upon approach.
+ Developing integrated study management plans with the core project team and/or sub-team.
+ Accountable for the execution of clinical studies, or assigned portion of clinical studies
+ Set objectives of the core project team and/or sub-team(s) according to agree upon contract, strategy and approach, effectively communicate and assess performance
+ Collaborate with other functional groups within the company where necessary to support milestone achievement and to manage study issues and obstacles.
+ Monitor progress against Contract and prepare/present project and/or sub-team information proactively to stakeholders internally and externally
+ Manage risk (positive and negative) and contingencies proactively and lead problem solving and resolution efforts
+ Achieve project quality by identifying quality risks and issues, responding to issues raised by project team and/or sub-team members and planning/implementing appropriate corrective and preventative action plans.
+ Responsible for ensuring the financial success of the overall project and/or project sub-team.
+ Forecast and identify opportunities to accelerate activities to bring revenue forward.
+ A bachelor’s degree in science or other related field combined with a minimum 3-5 years’ clinical research experience including a minimum of 18 months prior experience within project management of clinical trials within a pharma company or CRO
+ Successfully led and driven a cross-functional project team to meet customer expectations
+ Excellent customer management skills
+ Demonstrated ability to deliver results to the appropriate quality and timelines
+ Ability to manage key stakeholders across the business and work collaboratively with colleagues from various functional areas
+ Analytical and problem-solving skills
+ An in-depth knowledge of, and skill in applying, applicable clinical research regulatory requirements and Good Clinical Practice (ICH & FDA) guidelines
+ Experience working on Phase I or Early Clinical Development studies
+ Experience in managing the full project lifecycle
At IQVIA, 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. The advanced analytics, technology solutions and contract research services we provide to the life sciences industry are made possible by our 70,000+ employees around the world who apply their insight, curiosity and intellectual courage every step of the way. Learn more at jobs.iqvia.com .
IQVIA is a world leader in using data, technology, advanced analytics, and expertise to help customers drive healthcare – and human health – forward. Together with the companies we serve, we are enabling a more modern, more effective and more efficient healthcare system, and creating breakthrough solutions that transform business and patient outcomes.
To get there, it takes diverse skills and a curiosity to explore new possibilities. No matter your role, everyone at IQVIA, including our colleagues at Q² Solutions, contributes to our shared goal of improving human health. Thank you for your interest in growing your career with us.
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