# Clinical Research Associate 2 (CRA2)

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

**Apply**: https://fortrea.wd1.myworkdayjobs.com/en-US/Fortrea/job/Barcelona/Clinical-Research-Associate-II---Barcelona_265086?utm_source=yubhub.co&utm_medium=jobs_feed&utm_campaign=apply
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## Description

Fortrea's FSP team is currently seeking two CRA2 professionals to join the team in Barcelona. Candidates must have at least 3-4 years of experience working on complex clinical trials, specifically within Oncology (Lung cancer in early phase) / Immunology / Hypertension.

**Responsibilities:**

- Monitor study sites, including routine monitoring and closeout of clinical sites, maintenance of study files, and conduct of pre-study and initiation visits

- Liaise with vendors and perform other duties as assigned

- Ensure study staff have received proper materials and instructions to safely enter patients into the study

- Verify informed consent procedures and protocol requirements are adhered to according to regulatory requirements

- Review source documents to ensure data integrity

- Monitor data for missing or implausible data

- Ensure audit readiness at the site level

- Travel, including air travel, may be required

- Prepare accurate and timely trip reports

- Interact with internal work groups to evaluate needs, resources, and timelines

- Act as contact for clinical trial supplies and other suppliers

- Manage registry management as prescribed in project plans

- Perform feasibility work when requested

- Participate in and follow-up on Quality Control Visits (QC) when requested

- Recruit potential investigators, prepare EC submissions, and notify regulatory authorities

- Assist Senior CRA with managing investigator site budgets

- Track and follow-up on Serious Adverse Event (SAE) reporting

- Independently perform CRF review, query generation, and resolution against established data review guidelines

**Qualifications:**

- University degree in a scientific or medical field

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

- Fluent in Spanish and English, both written and verbal

**Experience:**

- Minimum 3-4 years of experience as an independent monitor, working in Immunology / Hypertension clinical studies

- 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
- Regulatory Guidelines
- Clinical Trials

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