# CRA II

**Company**: Fortrea
**Location**: Madrid
**Work arrangement**: onsite
**Experience**: senior
**Job type**: full-time
**Category**: Healthcare
**Industry**: Healthcare

**Apply**: https://fortrea.wd1.myworkdayjobs.com/en-US/Fortrea/job/Madrid/Clinical-Research-Associate--CRA----Regionalized-Galicia---Maternity-Leave-Cover_266488?utm_source=yubhub.co&utm_medium=jobs_feed&utm_campaign=apply
**Canonical**: https://yubhub.co/jobs/job_7976fb0c-328

## Description

Fortrea's FSP team is currently seeking two CRA II professionals to join the team in Galicia.

**Summary of Responsibilities:**

- Clinical site monitoring: conducts routine, pre-study, initiation, and close-out visits, ensuring full compliance with project plans.

- Site and patient protection: ensures informed consent, protocol adherence, and regulatory compliance to safeguard study participants.

- Data quality oversight: performs source document verification, CRF review, and manages data queries to ensure accuracy and completeness.

- Operational site management: prepares trip reports, ensures audit readiness, manages study files, coordinates with vendors, and uses resources efficiently.

- Safety reporting: tracks and follows up on Serious Adverse Events (SAEs), supporting report and narrative preparation.

- Extended support activities: feasibility assessments, QC visits, EC submissions, budget support, training/mentoring of new staff, and local project coordination.

- Cross-functional communication & logistics: liaises with internal teams, manages study materials, and travels as required.

**Qualifications (Minimum Required):**

- University Degree in Scientific / Medical Field

- Thorough understanding of ICH GCP Guidelines and understanding of local regulatory requirements in Spain

- Fluent in Spanish and in English, both written and verbal.

**Experience (Minimum Required):**

- Minimum 2 years of experience as independent monitor, working specifically within oncology: Prostate and Bladder cancer.

- Basic understanding of Regulatory Guidelines.

- Ability to work within a project team.

- Good planning, organization, and problem-solving skills.

- Good computer skills with good working knowledge of a range of computer packages.

- Valid Driver's License

## Skills

### Required
- ICH GCP Guidelines
- Spanish
- English
- oncology
- Prostate cancer
- Bladder cancer
- Regulatory Guidelines
- project management

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Source: [Apply at fortrea.wd1.myworkdayjobs.com](https://fortrea.wd1.myworkdayjobs.com/en-US/Fortrea/job/Madrid/Clinical-Research-Associate--CRA----Regionalized-Galicia---Maternity-Leave-Cover_266488?utm_source=yubhub.co&utm_medium=jobs_feed&utm_campaign=apply)