Associate Director, Clinical Science - Radiopharma Oncology

Bristol Myers Squibb; San Diego (CA); On-site; USD 191,000 - 231,000; Full time

Job summary

RayzeBio, a Bristol Myers Squibb subsidiary, seeks an Associate Director of Clinical Science to support radiopharmaceutical oncology programs. You will collaborate with clinical development to manage trial start-up, execution, close-out, data analysis, and regulatory documentation under MD supervision.

Strong communication and cross-functional teamwork are essential. You will help design studies, review protocols, and prepare regulatory submissions while navigating FDA/EMA guidelines and

Qualifications

• MS with a 6+ years of relevant drug development experience OR BS in Biological Sciences, health care, or a related field with 8+ years of relevant drug development experience.

Responsibilities

• Develop or oversee study concepts, synopses, and protocols.
• Review study design discussions and contribute to scientific decisions.
• Prepare study protocols, amendments, investigator materials, and manuals with supervision.
• Contribute to CRF design, Data Management Manuals, and Data Analysis Plans.
• Support preparation/review of INDs, regulatory documents, NDA/MAA filings.
• Coordinate teams and lead components of strategic initiatives.
• Summarize literature to integrate new study development.

Skills

Clinical trial design

Protocol development

Regulatory knowledge

Cross-functional collaboration

Data analysis

Microsoft Office

SpotFire

Communication skills

Education

MS with 6+ years drug development OR BS with 8+ years

Tools

SpotFire

Microsoft Office

Job description

RayzeBio, a Bristol Myers Squibb subsidiary, seeks an Associate Director of Clinical Science to support radiopharmaceutical oncology programs. You will collaborate with clinical development to manage trial start-up, execution, close-out, data analysis, and regulatory documentation under MD supervision.

Strong communication and cross-functional teamwork are essential. You will help design studies, review protocols, and prepare regulatory submissions while navigating FDA/EMA guidelines and