Scientific Director, Hematology Clinical Development
AbbVie
June 24, 2026
Remote friendly (South San Francisco, CA)
United States
$160,500 - $305,000 USD yearly
Clinical Research and Development
Purpose:
With supervision, oversees the direction, planning, execution and interpretation of clinical trials or research activities of a clinical development program. Participates in cross-functional teams to generate, deliver and interpret high-quality clinical data.
Responsibilities:
- Manages the design and implementation of study protocols (with appropriate supervision) in support of the Product Development Plan; oversees project-related education for investigators, study site personnel and AbbVie study staff.
- Reviews, interprets, and communicates accumulating safety and efficacy data; with Clinical Operations, may oversee study enrollment and overall timelines for key deliverables.
- Contributes to design, analysis, interpretation and reporting of scientific content for protocols, Investigator Brochures, Clinical Study Reports, regulatory submissions/responses, and other program documents.
- May contribute to development of a cross-functionally-aligned Clinical Development Plan.
- Participates in opinion leader interactions with Medical Affairs, Commercial and other functions as required.
- Stays current via conferences, medical literature, and training to augment therapeutic area expertise.
- Understands and complies with regulatory requirements for clinical studies and global drug development; may contribute to regulatory responses and discussions.
- Ensures adherence to Good Clinical Practices, pharmacovigilance standards, standard operating procedures, and other quality standards.
Qualifications:
- Bachelor’s degree in the sciences; advanced degree (MS, PhD) preferred.
- Ability to provide input and direction to clinical research with appropriate supervision.
- Strong desire to collaborate in a cross-functional setting.
- Clinical trial experience in pharmaceutical industry/academia (or equivalent) preferred.
- Knowledge of clinical trial methodology and regulatory/compliance requirements; experience designing study protocols desirable.
- Ability to interact externally and internally to support global scientific and business strategy.
- Excellent oral and written English communication skills.
With supervision, oversees the direction, planning, execution and interpretation of clinical trials or research activities of a clinical development program. Participates in cross-functional teams to generate, deliver and interpret high-quality clinical data.
Responsibilities:
- Manages the design and implementation of study protocols (with appropriate supervision) in support of the Product Development Plan; oversees project-related education for investigators, study site personnel and AbbVie study staff.
- Reviews, interprets, and communicates accumulating safety and efficacy data; with Clinical Operations, may oversee study enrollment and overall timelines for key deliverables.
- Contributes to design, analysis, interpretation and reporting of scientific content for protocols, Investigator Brochures, Clinical Study Reports, regulatory submissions/responses, and other program documents.
- May contribute to development of a cross-functionally-aligned Clinical Development Plan.
- Participates in opinion leader interactions with Medical Affairs, Commercial and other functions as required.
- Stays current via conferences, medical literature, and training to augment therapeutic area expertise.
- Understands and complies with regulatory requirements for clinical studies and global drug development; may contribute to regulatory responses and discussions.
- Ensures adherence to Good Clinical Practices, pharmacovigilance standards, standard operating procedures, and other quality standards.
Qualifications:
- Bachelor’s degree in the sciences; advanced degree (MS, PhD) preferred.
- Ability to provide input and direction to clinical research with appropriate supervision.
- Strong desire to collaborate in a cross-functional setting.
- Clinical trial experience in pharmaceutical industry/academia (or equivalent) preferred.
- Knowledge of clinical trial methodology and regulatory/compliance requirements; experience designing study protocols desirable.
- Ability to interact externally and internally to support global scientific and business strategy.
- Excellent oral and written English communication skills.