Oncology Clinical Sciences Lead

Moderna; Cambridge (MA); Hybrid; USD 180,000 - 230,000; Full time

Benefits offered by this job

Healthcare benefits

Well-being programs

Family planning benefits

Generous paid time off

Financial planning and retirement

Job summary

Moderna in Cambridge, MA is seeking a Senior Clinical Data Quality Scientist to support Oncology Therapeutic programs, assisting the Clinical Study Lead in Phase 1-3 studies. The role focuses on ensuring rigorous data quality to support governance and regulatory submissions.

You'll oversee end-to-end trial activities with the Clinical Study Lead, contribute to study design, data monitoring, analysis, and reporting, and help prepare Investigator Meetings and regulatory documents.

Qualifications

• Advanced degree in a scientific discipline with oncology knowledge.
• Experience in pharmaceutical/biotechnology clinical development.
• Strong data integrity, analysis, and data presentation skills.

Responsibilities

• Oversee end-to-end delivery of trial protocols, study design, initiation, safety monitoring, data dissemination and closeout.
• Coordinate site activation and subject enrollment across global studies with the Clinical Study Lead.
• Design study parameters to minimize risk and improve site performance and efficiency.
• Participate in inspection readiness activities for audits and regulatory inspections.
• Collaborate on Investigator Meetings, engagements, and regulatory document development.

Skills

Oncology knowledge

Clinical data quality

Team collaboration

Travel readiness

Education

PhD/PharmD/Masters or advanced nursing degree

Tools

Medidata Rave

Elluminate

Spotfire

Job description

Moderna in Cambridge, MA is seeking a Senior Clinical Data Quality Scientist to support Oncology Therapeutic programs, assisting the Clinical Study Lead in Phase 1-3 studies. The role focuses on ensuring rigorous data quality to support governance and regulatory submissions.

You'll oversee end-to-end trial activities with the Clinical Study Lead, contribute to study design, data monitoring, analysis, and reporting, and help prepare Investigator Meetings and regulatory documents.