Strategic Clinical Lead, Early Oncology Development

BioSpace

Cambridge (MA)

On-site

USD 180,000 - 240,000

Full time

17 hours ago
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Benefits offered by this job

High-quality healthcare
Prevention and wellness programs
14 weeks gender-neutral parental leave
Rewards package

Job summary

Sanofi is seeking a Clinical Lead for Early Development and Experimental Therapeutics in Oncology. The role focuses on leading translational and early clinical activities for oncology assets, coordinating cross-functional teams, and guiding trial design from preclinical through phase 2a.

The candidate will work with global asset teams, ensure high-quality documentation, and drive Go/No Go decisions while maintaining timelines and regulatory readiness.

Qualifications

  • MD or equivalent degree required and medical licensure expected.
  • Demonstrated ability to lead multidisciplinary teams in early clinical development.
  • Strong communication and collaboration skills across global teams.
  • Experience with translational medicine concepts and early-phase trials.

Responsibilities

  • Design safe, rapid First-In-Human studies for oncology assets.
  • Integrate development plans with therapeutic area strategy.
  • Provide clinical expertise to guide pre-clinical data generation and interpretation.
  • Make protocol design and safety decisions in early development.
  • Oversee study execution and medical monitoring.
  • Prepare regulatory documents and study reports with high quality.

Skills

Leadership
Cross-functional teamwork
Clinical development
Communication skills

Education

MD or equivalent

Job description

Sanofi is seeking a Clinical Lead for Early Development and Experimental Therapeutics in Oncology. The role focuses on leading translational and early clinical activities for oncology assets, coordinating cross-functional teams, and guiding trial design from preclinical through phase 2a.

The candidate will work with global asset teams, ensure high-quality documentation, and drive Go/No Go decisions while maintaining timelines and regulatory readiness.

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