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From the employer's careers site First seen 28 Oct 2026

CPM/Sr CPM

IQVIA Biotech senior full-time

Salary

zł217,800 - zł404,600

Apply on IQVIA Biotech

Description

IQVIA Biotech is recruiting for an experienced CPM/Sr CPM to join their respected, well-established team. The successful candidate will have a minimum of 4 years of regional/global CPM experience, with a strong background in working on Cardiovascular, Renal, or Metabolic trials.

The CPM/Sr CPM will be accountable for the execution of clinical studies, or assigned portions of clinical studies, per contract while optimizing speed, quality, and cost of delivery. Key responsibilities include:

  • Setting objectives for the core project team and assessing performance
  • Participating in bid defense presentations and leading smaller, less complex regional studies
  • Developing integrated study management plans with the core project team
  • Collaborating with other functional groups to support milestone achievement and manage study issues
  • Monitoring progress against contract and preparing project information for stakeholders
  • Managing risk and contingencies proactively and leading problem-solving efforts
  • Achieving project quality by identifying quality risks and issues and implementing corrective action plans
  • Serving as primary or backup project contact with customers and owning relationships with key customer contacts
  • Building and leading cross-functional project teams and managing project delivery
  • Ensuring financial success and forecasting opportunities to accelerate activities
  • Identifying changes in scope and managing change control processes
  • Providing input to line managers on project team members' performance
  • Supporting staff development and mentoring less experienced project team members

The role requires:

  • A Bachelor's degree in Life Sciences or a related field
  • 5 years of prior relevant experience, including > 1 year of project management experience
  • Advanced knowledge of job area, typically obtained through advanced education combined with experience
  • Knowledge of clinical trial conduct and skill in applying applicable clinical research regulatory requirements
  • Therapeutic area knowledge in Cardiovascular, Metabolic, or Renal would be an advantage
  • Good understanding of project financials and contractual obligations
  • Strong written and verbal communication skills, including excellent command of English
  • Strong customer service skills and presentation abilities
  • Ability to work across geographies and display high awareness of cultural differences

The potential base pay range for this role is zł217,800.00 - zł404,600.00.

Skills

Required

Nice to have

  • Cardiovascular
  • Metabolic
  • Renal
  • Obesity

Ready to apply?

You apply with the employer directly. Their original posting is here: https://iqvia.wd1.myworkdayjobs.com/en-US/IQVIA/job/Warsaw-Poland/Clinical-Project-Manager--IQVIA-Biotech_R1522841

Apply on IQVIA Biotech