# Clinical Data Review Lead

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

**Apply**: https://iqvia.wd1.myworkdayjobs.com/en-US/IQVIA/job/Madrid-Spain/Manager--Clinical-Trial-Safety_R1558025?utm_source=yubhub.co&utm_medium=jobs_feed&utm_campaign=apply
**Canonical**: https://yubhub.co/jobs/job_df387b79-1ff

## Description

We are seeking a Clinical Data Review Lead to oversee the review of clinical data for medical completeness, scientific accuracy, and coding consistency. You will be responsible for line management of a group of individuals and have shared accountabilities for service resulting in high-quality medical data review.

**Key Responsibilities:**

- Provide regular meetings with employees to discuss important business topics, workload, support needed, and performance development

- Perform work allocation and resource management duties

- Ensure compliance with corporate policies, procedures, and guidelines

- Oversee the process implementation and ongoing review and querying of critical clinical/safety data

- Ensure seamless and complete clinical data review

- Support scientists in day-to-day handling and querying of clinical/safety data

- Ensure effective cross-functional collaboration between staff and stakeholders

- Act as a trailblazer in clinical projects and a role model for project leaders/project experts

- Mentor and train junior staff to ensure consistent processes and efficient review of critical medical/safety data

**Requirements:**

- Advanced university degree in a medical/life science field

- Minimum 3 years of experience working in clinical research, pharmacovigilance, and/or safety and clinical data review methodology

- In-depth understanding of the clinical study and drug development process and GCP/ICH guidelines

- Proven project management capabilities and ability to manage change, risks, priorities, and performance targets

- Excellent knowledge of spoken and written English and computer proficiency

- Line management experience and ability to effectively lead complex non-drug projects in a worldwide environment

## Skills

### Required
- clinical research
- pharmacovigilance
- safety and clinical data review
- project management
- GCP/ICH guidelines
- English

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Source: [Apply at iqvia.wd1.myworkdayjobs.com](https://iqvia.wd1.myworkdayjobs.com/en-US/IQVIA/job/Madrid-Spain/Manager--Clinical-Trial-Safety_R1558025?utm_source=yubhub.co&utm_medium=jobs_feed&utm_campaign=apply)