The IQVIA sponsor-dedicated Clinical Functional Service Partnerships (Clinical FSP) department is supporting our client’s project team in the execution of clinical trials. 

We currently offer the exciting opportunity to join the team as Clinical Project Manager (m/f/d) in full-time and work home-based throughout Austria.

Responsibilities might include:

Manage the execution of clinical studies or assigned portion of clinical studies; including orchestration of local trial team, and integration with other functions as necessary throughout planning, conduct and closeout of trial. Ensure compliance with ICH-GCP and all other relevant regulatory regulations as well as accordance with client SOPs and values. 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 information proactively to stakeholders internally and externally.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.Build the cross-functional project team and lead their efforts; responsible for managing cross-collaboration of the core team and for overall project delivery to support milestone achievement and to manage study issues and obstacles.Ensure the financial success of the project, while optimizing speed, quality and cost of delivery. Forecast and identify opportunities to accelerate activities to bring revenue forward.Participate in bid defense presentations in partnership with Business Development.May be assigned as the primary contact for vendors leading project vendor management and vendor management related activities as per project requirements.

Required knowledge, skills and experience:

Bachelor’s or higher-level degree preferable in life science.Min. 1 year of prior relevant experience including project management experienceExpertise in covering clinical trialsKnowledge of applicable clinical research regulatory requirements, i.e., Good Clinical Practice (GCP) and International Conference on Harmonization (ICH) guidelines.Fluent languages skills in German on at least C1 level and good command of English.Computer skills including working knowledge of Microsoft Word, Excel and PowerPoint.Effective communication, organizational and planning skills.Planning, time management and prioritization skills while working on multiple projects.Excellent leadership skills, and the ability to establish and maintain effective working relationships with coworkers, managers and clients.Flexibility to business travel for client meetings and maybe occasional site visits.

What you can expect:

Resources that promote your career growthLeaders that support flexible work schedulesPrograms to help you build your therapeutic knowledgeDynamic work environments that expose you to new experiencesHome-office, accident insurance and moreMonthly gross salary: starting at 4.300 EUR basic - an overpay according to skills and working experience is possible

Whatever your career goals, we are here to ensure you get there!

Please apply with your English CV and motivation letter.

IQVIA is a leading global provider of clinical research services, commercial insights and healthcare intelligence to the life sciences and healthcare industries. We create intelligent connections to accelerate the development and commercialization of innovative medical treatments to help improve patient outcomes and population health worldwide. Learn more at https://jobs.iqvia.com