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Overview:
Clinical Project Management is focused on project delivery, productivity and quality resulting in strong financial performance and customer satisfaction.
Local Associate Project Manager is a member of the core project team responsible for project delivery of clinical studies to meet contractual requirements in accordance with SOPs, policies and practices.

Essential Functions:
• Provide input in to the development of integrated study management plans with the core project team and/or sub-team.
• Accountable for assigned clinical studies while optimizing speed, quality and cost of delivery and ensuring consistent use of study tools and training materials and compliance with standard processes, policies and procedures.
• Set objectives of project sub-team(s), according to agreed upon contract, strategy and approach, effectively communicate and assess performance..
• Monitor progress against contract and prepare/present project and/or sub-team information proactively to internal stakeholders. Support the project leader to prepare/present project and/or sub-team information proactively to external stakeholders.
• Identify risk (positive and negative) and contingencies and partner with project leader in problem solving and resolution efforts.
• Achieve project quality by identifying quality risks and issues, responding to issues raised and partner with project leader in planning/implementing appropriate corrective and preventative action plans.
• Support the project leader in ensuring the financial success of the project.
• Forecast and identify opportunities to accelerate activities to bring revenue forward in partnership with the senior project leader.
• Identify changes in scope and partner with project leader to manage change control process as necessary.
• Identify lessons learned and implement best practices.
• May be assigned as the primary contact for vendors leading project vendor management and vendor management related activities as per project requirements

Qualifications:
• Bachelor's Degree In life sciences or related field required.
• 2+ years clinical research experience in Clinical Project Management and Site monitoring
• Knowledge of principles, theories, and concepts of a job area.
• Knowledge of clinical trial conduct, and skill in applying clinical research regulatory requirements i.e. ICH GCP and relevant local laws, regulations and guidelines, towards clinical trial conduct. Broad protocol knowledge, therapeutic knowledge desired.
• Strong written and verbal communication skills including good command of English language. Strong presentation skills.
• Strong problem solving skills.
• Planning, time management and prioritization skills. Ability to organize resources needed to accomplish tasks, set objectives and provide clear direction to others, experience planning activities in advance and taking account of possible changing circumstances.
• Ability to handle conflicting priorities.
• Attention to detail and accuracy in work. Results-oriented approach to work towards delivery and output.
• Good software and computer skills
• Ability to establish and maintain effective working relationships with coworkers, managers and clients. Strong customer service skills.

• Good understanding of project financials.
• Hungary base, fluent in Hungarian and English.

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