Senior Scientific Director, Oncology Clinical Development – Hematology

This is a fully remote position, open to applicants in Oregon.

📋 Description

• Directs the strategy, planning, and interpretation of clinical trials or research initiatives for one or more clinical development programs.

• Engages in and may lead cross-functional teams to produce, deliver, and disseminate high-quality clinical data that supports the overall scientific and business strategy of the product.

• Manages project-related training for investigators, study site personnel, and AbbVie study staff.

• May be tasked with leading clinical study teams, ensuring overall study integrity, and reviewing, interpreting, and communicating accumulating data related to the safety and efficacy of the molecule.

• Holds responsibility for the design, analysis, interpretation, and reporting of scientific content for protocols, Investigator Brochures, Clinical Study reports, regulatory submissions and responses, and other program documents.

• May oversee the efforts of Medical and/or Scientific Directors and Clinical Scientists involved in the same or related programs.

• May participate in or co-chair Integrated Evidence Strategy Team(s), tasked with developing a comprehensive, cross-functionally-aligned, vetted Clinical Development Plan that fully considers contingencies and alternative strategies.

• Acts as the clinical lead and actively seeks interactions with opinion leaders in relation to the disease area(s).

• Responsible for comprehending regulatory requirements related to clinical studies and global drug development, and is accountable for adhering to these requirements.

⛳️ Requirements

• Bachelor's degree in the sciences; advanced degree (e.g., MS, PhD) is preferred.

• Experience in hematology is preferred.

• A minimum of 8 years of clinical trial experience in the pharmaceutical industry, academia, or a similar field.

• Capability to independently manage a complex clinical research program.

• Demonstrated leadership skills with the ability to inspire others within a cross-functional global team.

• Must be capable of leading through influence.

• Ability to engage with both external and internal stakeholders to support a global scientific and business strategy.

• Extensive understanding of clinical trial methodology, regulatory and compliance standards governing clinical trials, and experience in developing clinical strategies and designing study protocols.

• Excellent verbal and written communication skills in English are essential.

• Ability to exercise sound judgment, tackle complex problems, and devise solutions for one or more projects.

🏝️ Benefits

• Paid time off (vacation, holidays, sick leave).

• Medical, dental, and vision insurance.

• 401(k) plan available to eligible employees.

• Participation in short-term incentive programs.