Clinical Research Associate
Bristol Myers Squibb
full-time
Posted on:
Location Type: Office
Location: Madrid • 🇪🇸 Spain
Visit company websiteJob Level
JuniorMid-Level
Tech Stack
Google Cloud Platform
About the role
- Conduct site qualification, initiation, routine monitoring and close-out visits across all trial phases
- Maintain the ethical and scientific integrity of clinical trials by verifying data
- Monitor site adherence to ICH GCP and local regulations
- Cultivate and sustain effective relationships with internal cross-functional teams and external partners
- Prepare and submit written reports, both monitoring and administrative
- Assess potential Investigators and their sites to ensure sufficient resources and capabilities
- Identify, assess, and prioritize risks at the site and study level
- Serve as a key resource for colleagues, providing guidance and mentoring
Requirements
- Bachelor’s degree required, preferably within life sciences or equivalent
- Valid driver’s license (as locally required)
- Clinical Research Associate: 2-3 years of relevant clinical research experience
- Relevant prior Pharma/Biotech Sponsor employment or experience as a clinical study coordinator preferred
- Experience in the drug discovery/development process
- Knowledge and understanding of clinical research processes, regulations and methodology
- Working knowledge of ICH/GCP Guidelines and applicable local laws and regulations
- Proven ability to work independently with a high degree of autonomy
- Proficient in navigating and utilizing multiple clinical systems (e.g., CTMS, eTMF, RBQM dashboards)
Benefits
- wide variety of competitive benefits
- services and programs
Applicant Tracking System Keywords
Tip: use these terms in your resume and cover letter to boost ATS matches.
Hard skills
clinical researchdata verificationrisk assessmentmonitoringreport preparationsite qualificationsite monitoringinvestigator assessmentdrug discoverydrug development
Soft skills
relationship buildingmentoringguidanceindependenceautonomy