Integrative Science Lead: Cross-Functional CGT Strategy

Astellas Pharma; Westborough (MA); On-site; USD 145,000 - 208,000; Full time

Benefits offered by this job

Medical insurance

Dental insurance

Vision insurance

401(k) match

Bonus programs

PTO & holidays

Job summary

Astellas Pharma in Westborough, MA is seeking an Integrative Science Lead to serve as a central liaison across CGT programs, translating cross-functional needs into clear IS activities, deliverables, ownership, and resource plans. This on-site role requires leadership in a dynamic, matrixed environment.

The role focuses on integrating Bioanalytical, Cytogenomics, Preclinical Development, Study Management, and Preclinical Writing to support planning, execution, interpretation and regulatory

Qualifications

• Relevant experience in pharmaceutical or biotechnology research and development.
• Strong knowledge of cell and gene therapy; regulatory interactions and preclinical support.
• Ability to operate in a matrixed environment with strong communication skills.

Responsibilities

• Represent Integrative Science in initiatives, programs, and governance forums.
• Translate needs into clear IS activities, deliverables, timelines and ownership.
• Coordinate across Bioanalytical, Cytogenomics, Preclinical Development and Study Management.
• Maintain visibility of IS commitments and prioritize activities by scientific importance.
• Communicate risks and recommendations to internal customers and governance forums.

Skills

Integrative Science

Cell & Gene Therapy

Communication skills

Matrixed environment

Presentation skills

Education

PhD preferred

Job description

Astellas Pharma in Westborough, MA is seeking an Integrative Science Lead to serve as a central liaison across CGT programs, translating cross-functional needs into clear IS activities, deliverables, ownership, and resource plans. This on-site role requires leadership in a dynamic, matrixed environment.

The role focuses on integrating Bioanalytical, Cytogenomics, Preclinical Development, Study Management, and Preclinical Writing to support planning, execution, interpretation and regulatory