Executive Director, Global Medical Affairs Disease Area Lead, Solid Tumors

About the role

The Senior Disease Area Lead, GMA, supports BeOne Clinical and Medical assets by successfully executing the Global Medical Affairs program and Clinical Development strategy. This role reports to the Vice President, Global Medical Affairs.

Responsibilities

• Develop, lead, and execute the gynecologic Global Medical Affairs Plan and future solid tumor plans based on pipeline data advancements.
• Develop and execute data generation strategies, including investigator-initiated programs and real-world evidence programs.
• Represent Medical Affairs in early development and clinical development team meetings, contributing regional and global medical input to the clinical development plan, clinical trial design, and successful implementation of the clinical program.
• Influence and support the development of disease and product-specific Clinical Development strategy within thoracic cancers.
• Lead the scientific communications team on a successful Disease Area publication strategy and implement a successful publication plan, including review and approval of relevant abstracts and manuscripts.
• Lead and work cross-functionally with Clinical Development on disease area advisory meetings.
• Interpret and present clinical trial data both internally and externally.
• Partner with the Health Economics and Outcomes Research Team to provide technical and clinical expertise on relevant disease area evidence generation studies.
• Train BeOne colleagues, CRO staff, and study site staff on the therapeutic area, molecule, and/or clinical protocols.
• Contribute to or perform therapeutic area/indication research and competitor analysis.
• Build and maintain strong relationships with key opinion leaders and institutions globally.
• Build strong alliances and relationships with internal experts.
• When appropriate, be the GMA representative at Alliance partnerships.
• Develop, track, execute, and report on goals and objectives.
• Support budget planning and management.
• Be accountable for compliant business practices.

Qualifications and Experience

• Advanced degree (MD, PharmD, PhD, or MD equivalent) with subspecialty training in oncology.
• Extensive experience in pharma/biotech in solid tumors is required.
• 8+ years of experience within other biotech/pharmaceutical companies.
• Clinical solid tumor oncology experience is mandatory for this role.
• Previous experience in Clinical Development in the role of medical director or clinical scientist is strongly preferred.
• Expert understanding of global clinical study design and drug development process from discovery to registration and post-marketing.
• High level of communication (written and verbal), interpersonal, organizational, and cross-functional collaboration skills.
• Knowledge of GCP and ICH Guidelines.
• Flexibility to work with colleagues in a global setting.
• Able to engage in work-related travel approximately 25%.
• Strategic leader with demonstrated success building, managing, and developing individuals and teams is preferred.
• Experience with the development and support of related SOPs and policies is expected.
• Knowledge of industry-standard Clinical Development IT solutions is expected.
• Ability to influence and lead.
• Exceptional cross-functional collaboration within GMA and with other departments.
• Accountable and results-driven.
• Impactful written and verbal scientific communication.
• Problem-solving and risk-mitigation skills.
• Confident, positive attitude.
• Flexibility and embracing change.

Salary Range

$296,600.00 - $376,600.00 annually