As a Sr Clinical Project Manager, you will manage the delivery of clinical research studies from study award to closeout and ensure that quality deliverable are presented on time and within budget. You will coordinate work streams and cross-functional project teams while monitoring the use of consistent tools and methodologies, you will also be primary point of contact with the project sponsors. Other key responsibilities will include:

• Accountable for the global and / or local execution of assigned clinical studies, or assigned portion of clinical studies

• Developing integrated study management plans with the core project team and/or sub-team.

• 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.

• Contributing to the development of the project delivery strategy for RFPs. Participate in bid defense preparations. Understand project strategy and translate the agreed upon approach.

• 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.

About you:

You will be an experienced Clinical Project Manager who will have the passion to succeed, ability to multi task and balance stakeholder expectations. Other key requirements will include:

• Proven leadership skills including strong work ethic, ability to work with different teams and ability to think laterally when needed

• Ideally between 2-3 years professional experience with a bachelor’s degree in Life Sciences or related field

• Ph I Healthy Volunteer /early phase and patient study experience is highly regarded

• Ability to pivot study strategy quickly and lead teams in the right direction

• Ph I Healthy Volunteer /early phase and patient study experience is highly regarded

• In depth knowledge of applicable clinical research regulatory requirements; i.e., Good Clinical Practice (GCP) and International Conference on Harmonization (ICH) guidelines

• Broad protocol knowledge; therapeutic knowledge is desired

• Strong understanding of Clinical Research industry (drug/device/technology/etc.) and the relevant environments in which it operates

• Project management practices and terminology

• Experience monitoring the use of consistent tools and methodologies

• Full risk management experience and ability to mitigate

• Strong understanding of project financials

• Excellent communication and rapport building skills 

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 67,000+ employees around the world who apply their insight, curiosity and intellectual courage every step of the way. Learn more at jobs.iqvia.com.