Lead Clinical Research Scientist - Oncology Trials

Genmab; Lombardia; On-site; EUR 98,000 - 147,000; Full time

Benefits offered by this job

Pension

Health insurance and wellness benefits

Paid time off

Employee support programs

Job summary

Genmab is seeking an Ad, Clinical Research Scientist to lead or co-lead clinical trials with close collaboration across Medical Director, cross-functional teams and CROs. The role emphasizes development of CDP, regulatory submissions, and scientific data interpretation.

The candidate should have 8+ years in clinical research, with 4+ years in drug development, preferably oncology/hematology, and a proven ability to work in a matrixed environment under tight timelines.

Qualifications

• PhD/Pharm D/MS or equivalent degree in medical/biological/pharmaceutical sciences.
• 8+ years of clinical research experience with 4+ years in drug development (oncology/hematology preferred).
• Experience working in a matrixed, project-oriented team environment.
• Proven performance in prior roles and in collaborative settings.
• Ability to perform under pressure in a fast-paced environment and meet tight timelines.

Responsibilities

• Lead or co-lead one or more clinical trials within a therapeutic area.
• Contribute to program strategy and clinical development plan.
• Author protocol, ICF, IB, safety updates, study reports, and regulatory submissions.
• Develop eCRF components and provide data management support.
• Lead data review, summarize efficacy and safety data for analyses.
• Provide medical input for country/site selection and feasibility assessments.
• Coordinate committee meetings and prepare presentations for Investigator meetings.
• Collaborate with project teams and CROs on study plans and governance.
• Prepare communications for Scientific Communications and publications.
• Mentor junior Clinical Research Scientists.

Skills

PhD

Pharm D

MS

Equivalent degree

Clinical research

Team collaboration

Work under pressure

Proactivity

Job description

Genmab is seeking an Ad, Clinical Research Scientist to lead or co-lead clinical trials with close collaboration across Medical Director, cross-functional teams and CROs. The role emphasizes development of CDP, regulatory submissions, and scientific data interpretation.

The candidate should have 8+ years in clinical research, with 4+ years in drug development, preferably oncology/hematology, and a proven ability to work in a matrixed environment under tight timelines.