# CPM/Sr CPM

**Company**: IQVIA Biotech
**Experience**: senior
**Job type**: full-time
**Category**: Healthcare
**Industry**: Healthcare

**Apply**: https://iqvia.wd1.myworkdayjobs.com/en-US/IQVIA/job/Madrid-Spain/Senior-Clinical-Project-Manager--Oncology---IQVIA-Biotech_R1532843?utm_source=yubhub.co&utm_medium=jobs_feed&utm_campaign=apply
**Canonical**: https://yubhub.co/jobs/job_bd36ad4c-d52

## 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 and a strong background in working on Oncology trials.

The Clinical Project Management team at IQVIA Biotech focuses on project delivery, productivity, and quality, resulting in strong financial performance and customer satisfaction. As a CPM/Sr CPM, you will be accountable for the execution of clinical studies, setting objectives for the core project team, and effectively communicating and assessing performance.

Key responsibilities include:

- Executing clinical studies per contract while optimizing speed, quality, and cost of delivery

- 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 ideal candidate will have:

- 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

- Broad protocol knowledge and therapeutic area knowledge in areas such as cardiovascular-metabolic, renal, or obesity

- Good understanding of project financials and experience managing 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 and understanding of cultural differences

## 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/Madrid-Spain/Senior-Clinical-Project-Manager--Oncology---IQVIA-Biotech_R1532843?utm_source=yubhub.co&utm_medium=jobs_feed&utm_campaign=apply)