Executive Clinical Program Leader - Translational Clinical Oncology

Novartis AG; Cambridge (MA); Presencial; USD 288.000 - 536.000; Jornada completa

Ventajas ofrecidas por este puesto de trabajo

Insurance plans

Retirement plans

Wellbeing resources

Global recognition programs

Hybrid working options

14 weeks parental leave

Descripción de la vacante

Novartis is seeking an Executive Clinical Program Leader to provide strategic medical leadership across early oncology development programs in the Translational Clinical Oncology portfolio. The role spans from target identification through transition to later-stage development, collaborating with cross-functional teams to accelerate decision-making and portfolio advancement.

The ECPL will contribute scientific and clinical expertise to evaluate external opportunities, lead global programs, and

Formación

• MD/PhD or MD with clinical research track record.
• Board certification in Hematology-Oncology or equivalent.
• Extensive leadership of global early-phase hematology-oncology programs.

Responsabilidades

• Provide strategic medical and scientific leadership across early oncology development programs.
• Represent Translational Clinical Oncology programs at governance and leadership boards.
• Lead clinical strategy development and provide input for studies and preclinical projects.
• Review key study documents and regulatory submissions with scientific rigor.
• Contribute to business development, licensing evaluations, and portfolio reviews.
• Lead and oversee external collaborations and strategic partnerships.

Conocimientos

Leadership

Mentoring

Communication

Clinical research

GCP knowledge

Oncology drug development

Publications

Educación

MD/PhD

Board certification Hematology-Oncology

Descripción del empleo

Job Description Summary

Executive Clinical Program Leader - Translational Clinical Oncology

Location: Cambridge, MA, USA

Work Arrangement: Onsite

Employment Type: Full-Time

Job Description Summary

The Executive Clinical Program Leader (ECPL) provides strategic medical and scientific leadership for the development of multiple experimental agents within the Translational Clinical Oncology (TCO) portfolio. The role spans from early target identification through transition into later-stage development, partnering closely with development teams to accelerate decision-making and portfolio advancement. The ECPL also provides scientific and clinical expertise to evaluate external innovation opportunities and business development initiatives.

Key Responsibilities

• Provide strategic medical and scientific leadership across early oncology development programs.


• Represent Translational Clinical Oncology programs at internal governance and leadership boards.


• Lead clinical strategy development and provide senior clinical input for clinical studies and preclinical research projects.


• Review and provide feedback on key study documents, including protocols, investigator brochures, and regulatory submissions.


• Contribute scientific and clinical expertise to business development, licensing evaluations, and portfolio reviews.


• Lead and oversee external collaborations and strategic partnerships.


• Mentor colleagues and serve as an expert resource across Biomedical Research and the broader organization.


• Ensure the safe, ethical, and compliant conduct of clinical trials in accordance with GCP and company procedures.


• Engage with external experts, investigators, and health authorities in support of early oncology clinical development.


• Contribute to scientific publications, abstracts, and presentations for internal and external audiences.

Essential Requirements

• MD required; MD/PhD preferred.


• Board certification (or equivalent expertise) in Hematology-Oncology.


• 7+ years of experience leading complex global early-phase hematology-oncology clinical programs within the pharmaceutical or biotechnology industry.


• Strong experience in translational hematology/oncology and clinical research.


• Recognized scientific and clinical expertise demonstrated through publications and professional contributions.


• Broad knowledge of oncology drug development and clinical trial execution.


• Excellent written and verbal communication skills.


• Proven leadership and people management experience.


• Strong mentoring and talent development capabilities.


• High ethical standards and commitment to improving outcomes for patients with cancer.

Rewards

At Novartis, we're committed to reimagining medicine together - and rewarding the people who make it happen.

The rewards of being part of our team go far beyond base pay and incentives. We also offer a variety of competitive benefits in kind to help you thrive personally and professionally, such as insurance plans, retirement plans, wellbeing resources and global recognition programs. In addition, we provide flexible and hybrid working options, where possible, and a minimum of 14 weeks paid parental leave.

Expected Annual Base Salary Range for role:

USA: $288,400.00 - 535,600.00 USD Annual

The salary offered is determined based on gender-neutral objectives, such as relevant skills, competencies and experience in accordance with the Novartis pay setting policy and upon joining Novartis will be reviewed periodically.

In addition to your base salary, you may be eligible for a performance-based bonus depending on certain performance parameters. Further details will be provided during the application process.

Pay equity is a fundamental principle of our employment policy and reflects our commitment to create a diverse, equitable and inclusive environment that treats all employees with dignity and respect, as outlined in our Code of Ethics.

Read our brochure to learn more about our global total rewards offering: https://www.novartis.com/sites/novartis_com/files/novartis-life-handbook.pdf

Note: Benefits and compensation may vary by country and are subject to local legal requirements, including provisions of collective bargaining agreements where applicable. A full overview of your compensation package, including any relevant collective bargaining agreement details applicable to your role based on your employment location and Novartis employer entity, will be communicated separately to you during the application process.

Why Novartis

Helping people with disease and their families takes more than innovative science. It takes a community of smart, passionate people like you. Collaborating, supporting and inspiring each other. Combining to achieve breakthroughs that change patients' lives. Ready to create a brighter future together? https://www.novartis.com/about/strategy/people-and-culture

Benefits and Rewards: Read our handbook to learn about all the ways we'll help you thrive personally and