Assoc Clinical Project Manager

3 days ago

Prague, Hlavní město Praha, Czech Republic IQVIA Full time 900,000 - 1,200,000 per year

Job Overview
The 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. Clinical Project Management is focused on project delivery, productivity and quality resulting in strong financial performance and customer satisfaction.

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 portion of clinical studies as per the contract 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.
  • 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 internal stakeholders. Support the project leader to prepare/present project and/or sub-team information proactively to external stakeholders.
  • Identify risk and contingencies and partner with project leader in problem solving and resolution efforts. 
  • Lead the efforts of a project sub-team, responsible for managing cross-collaboration of the sub-team to support milestone achievement and to manage issues and obstacles. 
  • 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.
  • Minimum 2 years of clinical research experience, including project management and on-site monitoring (CRA).
  • Solid understanding of clinical trial processes, ICH GCP, and relevant regulations.
  • Broad protocol and therapeutic knowledge preferred.
  • Excellent problem-solving, planning, and time management abilities.
  • Detail-oriented with a results-driven mindset.
  • Skilled in MS Office (Word, Excel, PowerPoint).
  • Strong interpersonal and customer service skills; able to work effectively across cultures and geographies.
  • Good grasp of project financials and ability to manage competing priorities.
  • Proficient in Czech and English; strong written, verbal, and presentation skills.
  • Located in or near Prague.

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

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