Associate Director, Clinical Science – Oncology

Bristol Myers Squibb; San Diego (CA); Vor Ort; USD 191.000 - 231.000; Vollzeit

Benefits dieser Stelle

Flexible Time Off

11 paid holidays each year

Comprehensive benefits (medical/dental

Retirement planning

Zusammenfassung

RayzeBio, a wholly-owned subsidiary of Bristol Myers Squibb, seeks an Associate Director of Clinical Science to support radiopharmaceutical oncology clinical development. You will collaborate across clinical development, medical writing, and operations to drive trial start-up, execution, data analysis, and regulatory submissions, with AI tools to enhance productivity.

Role involves handling IND/NDAs/MAAs, data listings and study results, and may coordinate teams or lead components of strategic

Qualifikationen

• PharmD or PhD preferred.
• 6+ years of relevant drug development experience with an MS.
• 8+ years of relevant drug development experience with a BS degree in Biological Sciences, health care, or a related field.
• Minimum of 5 years' experience in clinical research or clinical pharmacology in a biotech/pharmaceutical company, contract research organization.

Aufgaben

• Acquire and utilize knowledge of clinical trial design for study concepts and protocols.
• Participate in protocol review discussions for study design.
• Prepare study protocols, amendments, and Investigator meeting materials under guidance.
• Contribute to CRFs, Data Management Manuals, and Data Analysis Plans.
• Review ongoing clinical data and organize Data Review Committee meetings.

Kenntnisse

Fast learner

Adaptable

Microsoft Office

SpotFire

FDA/EMA/ICH knowledge

Cross-functional collaboration

Ausbildung

PharmD or PhD preferred

MS in Biological Sciences or related field

BS in Biological Sciences or related field

Tools

Microsoft Office

SpotFire

Jobbeschreibung

RayzeBio, a wholly-owned subsidiary of Bristol Myers Squibb, seeks an Associate Director of Clinical Science to support radiopharmaceutical oncology clinical development. You will collaborate across clinical development, medical writing, and operations to drive trial start-up, execution, data analysis, and regulatory submissions, with AI tools to enhance productivity.

Role involves handling IND/NDAs/MAAs, data listings and study results, and may coordinate teams or lead components of strategic