Senior Oncology Clinical Data Scientist Lead

Precision Medicine Group; España; On-site; EUR 70,000 - 110,000; Full time

Job summary

Precision Medicine Group is seeking a Principal/Senior Clinical Scientist with extensive oncology experience to lead clinical science across assigned oncology, rare diseases, and autoimmune programs. You will oversee data review, interpretation, and data cleaning to ensure high-quality, protocol-compliant data and participant safety.

You will guide eCRF design, risk-based quality management, and collaboration with Medical Monitoring and study teams while supporting study deliverables within

Qualifications

• Bachelor's degree or equivalent in science/health discipline with proficiency in medical terminology
• Minimum of 8 years of clinical research experience
• Minimum of 3 years Oncology experience, within past 1.5 years
• Minimum of 1 year of leadership experience

Responsibilities

• Lead Clinical Science services per study scope from start to database lock
• Perform holistic individual and aggregate data review with clinical judgment
• Guide eCRF design, data capture requirements, edit checks, and data cleaning
• Support RBQM and risk review processes with cross-functional teams
• Collaborate with Medical Monitoring and study teams for data review findings
• Maintain eTMF documentation and participate in study meetings

Skills

Microsoft Office proficiency

English language proficiency

Data review platforms

Education

Bachelor's degree or equivalent in science/health discipline with medical terminology

8+ years clinical research experience

3+ years Oncology experience within past 1.5 years

1+ year leadership experience

Tools

Data review tools

Job description

Precision Medicine Group is seeking a Principal/Senior Clinical Scientist with extensive oncology experience to lead clinical science across assigned oncology, rare diseases, and autoimmune programs. You will oversee data review, interpretation, and data cleaning to ensure high-quality, protocol-compliant data and participant safety.

You will guide eCRF design, risk-based quality management, and collaboration with Medical Monitoring and study teams while supporting study deliverables within