# CPM/Sr CPM

**Company**: IQVIA Biotech
**Experience**: senior
**Job type**: full-time
**Salary**: zł217,800.00 - zł404,600.00
**Category**: Healthcare
**Industry**: Healthcare

**Apply**: https://iqvia.wd1.myworkdayjobs.com/en-US/IQVIA/job/Warsaw-Poland/Clinical-Project-Manager--IQVIA-Biotech_R1522841?utm_source=yubhub.co&utm_medium=jobs_feed&utm_campaign=apply
**Canonical**: https://yubhub.co/jobs/job_4bbf68bf-b96

## 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
- Life Sciences
- Project Management
- Clinical Trial Conduct
- ICH GCP
- English

### Nice to have
- Cardiovascular
- Metabolic
- Renal
- Obesity

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Source: [Apply at iqvia.wd1.myworkdayjobs.com](https://iqvia.wd1.myworkdayjobs.com/en-US/IQVIA/job/Warsaw-Poland/Clinical-Project-Manager--IQVIA-Biotech_R1522841?utm_source=yubhub.co&utm_medium=jobs_feed&utm_campaign=apply)