Clinical Development Executive Medical Director, Hematology

Role Summary

Clinical Development Medical Executive Director within Hematology is responsible for defining and executing the development strategy of hematology programs. The role reports to the Global Development Product Lead and requires leading or supporting development programs, cross-functional collaboration, and representing programs externally. The position may oversee one or more clinical subteams and serve as the clinical lead across multiple trials.

Responsibilities

• May lead product specific Global Development Team
• Serves as the subject matter expert on clinical issues
• Work across the organization and on the cross-functional Global Development Team to lead, develop and execute the clinical development plan of one or more hematology indications in alignment with the Lifecycle Management Plan and Integrated Product Plan
• Endorses clinical decisions in advance of GPT, senior management reviews or governance bodies with the GDPL
• May provide oversight and management responsibilities of medical director(s)
• Accountable for the clinical development strategy, trial design, execution, and delivery of trial results with the GDPL
• Accountable for integrating regulatory, statistical and other internal and external stakeholder input into study designs
• Serves as primary interface with Development Review Committee
• Oversee the development and management of clinical protocols and amendments, investigator brochures, and clinical study reports
• Oversee the evaluation, interpretation, reporting and presentation of study data
• Accountable with safety for clinical evaluations and safety decisions, escalating to GDPL as necessary
• Accountable with clinical pharmacology for defining and identifying optimal dose and schedule selection
• Accountable with regulatory for health authority interactions, escalating to GDPL as necessary
• May participate in evaluating business development opportunities
• Conduct medical monitoring activities including eligibility assessment, data review and safety monitoring
• Lead peer-to-peer interactions with investigator
• Serve as the point of contact for clinical issues between the study team, investigators, ethics committees, steering committees, and regulatory authorities
• Lead and contribute to development and maintenance of clinical trial and regulatory documents, in collaboration with Clinical Scientist and the cross-functional team
• Oversee and provide clinical development leadership across several study teams
• Serves as the Clinical Development Lead on working groups and subteams including for Marketing Authorization Applications and in business development opportunities

Qualifications

• Required: Medical degree or advanced degree with relevant clinical/industry experience (typically 4+ years).
• Required: 7+ years industry experience
• Required: 5+ years of experience leading diverse teams
• Required: Prior management responsibilities of medical directors or clinical scientists
• Preferred: Board certified/eligible in oncology or equivalent
• Preferred: Experience across multiple phases of clinical development and across drug classes in oncology
• Preferred: Experience in leading NDA, BLA or MAA

Additional Requirements

• Global travel may be required
• Relocation assistance may be available
• Work location: hybrid role requiring you to live within commuting distance and work on-site an average of 2.5 days per week