About the job
As a Scientific Director in Oncology Clinical Development, you will play a pivotal role in the direction, planning, execution, and interpretation of clinical trials within a comprehensive clinical development program. Collaborating with cross-functional teams, you will ensure the generation and delivery of high-quality clinical data that supports both scientific and business strategies for our product pipeline.
Key Responsibilities:
- Manage the design and implementation of study protocols for clinical development programs, ensuring alignment with the overall Product Development Plan while adhering to medical and scientific principles as well as compliance and regulatory standards. Educate investigators, study site personnel, and AbbVie staff on project-related matters.
- Oversee the review, interpretation, and communication of safety and efficacy data related to the molecule, collaborating with Clinical Operations on study enrollment and timelines for critical deliverables.
- Contribute to the design, analysis, interpretation, and reporting of key scientific documents, including protocols and regulatory submissions.
- Assist in developing a robust Clinical Development Plan in collaboration with cross-functional team members.
- Engage with opinion leaders in the relevant disease areas and work alongside Medical Affairs and Commercial teams as needed, adhering to corporate policies.
- Stay updated on professional information and technological advancements through conferences and literature to enhance expertise in oncology.
- Understand and comply with regulatory requirements related to clinical studies and global drug development, contributing to regulatory discussions as necessary.
- Ensure compliance with Good Clinical Practices, pharmacovigilance standards, and all quality standards for conducting research.

