Executive Director, Clinical Science, Oncology, Thoracic, Lung, Head & Neck, and Gastrointestinal at Merck | Rahway, NJ | Rezi

Executive Director, Clinical Science, Oncology, Thoracic, Lung, Head & Neck, and Gastrointestinal at Merck

Executive Director, Clinical Science, Oncology, Thoracic, Lung, Head & Neck, and Gastrointestinal

Merck · Rahway, NJ

Today

Executive Director, Clinical Science, Oncology, Thoracic, Lung, Head & Neck, and Gastrointestinal

Merck · Rahway, NJ

5 hours ago
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About the Role

The Executive Director, Clinical Science is a senior leader within Oncology Clinical Development, responsible for strategic, scientific, operational, and people leadership across a portfolio of oncology programs. This role serves as a member of the Oncology Clinical Science Leadership Team, shaping the strategic direction and operational effectiveness of the Clinical Science organization. The Executive Director leads a large matrixed organization, ensuring scientific rigor, patient focus, quality, and regulatory readiness while championing innovation and modern ways of working.

Responsibilities

  • Holds accountability for portfolio delivery from the Clinical Science perspective, including prioritization, resource alignment, and support for key development milestones.
  • Provide strategic oversight for a portfolio of oncology assets across multiple therapeutic areas and stages of development.
  • Partner with Therapeutic Area Heads and leaders across Clinical Operations, Regulatory Affairs, Biostatistics and Data Management, Drug Safety and Pharmacovigilance, Translational Medicine, and Medical Affairs to drive development strategy execution.
  • Ensure Clinical Science contributions support development plans, regulatory submissions, health authority interactions, and lifecycle management activities.
  • Apply Clinical Science expertise to inform therapeutic area and portfolio strategy.
  • Optimize allocation of Clinical Science resources and associated budgets across a complex portfolio.
  • Serve as a senior escalation point for scientific and resource-related issues.
  • Establish and sustain high standards for scientific rigor, clinical science quality, medical data review, study oversight, and regulatory readiness.
  • Drive consistency in clinical science practices, study execution, and data interpretation.
  • Foster a culture of proactive risk identification, mitigation, inspection readiness, and continuous quality improvement.
  • Advance innovative approaches to medical data review, signal detection, study oversight, and evidence-based decision-making.
  • Champion adoption of AI-enabled, digital, and technology-driven capabilities that enhance Clinical Science productivity, quality, efficiency, and effectiveness.
  • Contribute to identifying opportunities to leverage advanced analytics, artificial intelligence, automation, and digital solutions.
  • Drive modernization of clinical data review through innovative approaches.
  • Foster a culture of innovation, experimentation, continuous learning, and responsible implementation of emerging technologies.
  • Partner with cross-functional stakeholders to define, develop, and implement scalable capabilities.
  • Lead, coach, and develop a high-performing Clinical Science organization.
  • Champion a culture of leadership excellence by guiding, developing, and holding accountable leaders at multiple levels.
  • Build organizational capability through talent planning, succession management, leadership development, and career growth strategies.
  • Create an inclusive environment that promotes engagement, psychological safety, accountability, collaboration, and continuous development.
  • Develop future leaders by mentoring Clinical Scientists and CS people leaders.
  • Ensure leaders are equipped to provide effective coaching, feedback, performance development, and career support.
  • Contribute to the development and execution of Clinical Science strategy, priorities, and long-term organizational objectives.
  • Lead initiatives related to organizational design, workforce planning, and resource optimization.
  • Develop and implement scalable operating models that balance portfolio execution, organizational effectiveness, employee development, and talent retention.
  • Lead cross-functional initiatives that improve efficiency, effectiveness, innovation, and organizational health.
  • Represent Clinical Science in governance forums, leadership discussions, and strategic planning activities.
  • Shape functional and enterprise priorities through leadership engagement, cross-functional partnerships, and influence across organizational boundaries.

Requirements

  • Advanced scientific or healthcare degree required (PhD, PharmD) + at least 10 years of oncology drug development experience OR Master’s Degree in life sciences + 15 years of oncology drug development experience
  • Significant experience in oncology drug development with demonstrated success across multiple phases of clinical development.
  • Deep expertise in Clinical Science, Clinical Development, and execution of global clinical programs.
  • Experience supporting regulatory submissions, health authority interactions, and late-stage development activities.
  • Proven leadership experience managing in large, matrixed organizations through multiple levels of management.
  • Demonstrated success developing talent, building leadership capability, and creating high-performing teams.
  • Familiarity with, or interest in emerging AI, advanced analytics, and digital capabilities applicable to clinical development.
  • Experience in the therapeutic areas of Thoracic, Lung, Head & Neck, and Gastrointestinal preferred.
  • Generate and consider options for action to achieve a long-range goal; develop decision criteria considering factors, such as cost, benefits, risks, timing and buy-in; select the strategy most likely to succeed.
  • Identify the key tasks and resources needed to achieve strategic objectives.
  • Offer a broad organizational perspective that goes beyond the goals of one’s immediate business unit or work role; question assumptions about existing relationships; demonstrate flexibility when forming and adjusting partnerships to achieve broader goals; show willingness to work across current boundaries.
  • Ensure that those responsible for implementing a strategic initiative have role clarity and accountability for required actions and outputs, as well as the direction and authority to act in a way consistent with organizational values.
  • Leverage environmental supports and remove development barriers; advocate for individual to higher levels of management to create development opportunities; provide guidance and positive models; seek suggestions for improving performance; collaboratively create development plans that include activities targeted to specific goals.
  • Create momentum by taking immediate action and encouraging others to take action to improve organizational culture, processes or products/services; offer resources and direction to support implementation; break down cultural and operational barriers to change; recognize and reward those who contribute to change efforts.

Skills

  • Advanced Analytics
  • Artificial Intelligence (AI)
  • Clinical Development
  • Clinical Sciences
  • Cross-Functional Leadership
  • Executive Leadership
  • Global Clinical Studies
  • Innovation
  • Matrix Leadership
  • Oncology
  • Oncology Drug Development
  • Regulatory Submissions
  • Strategic Leadership
  • Talent Development

Location

  • Domestic

Work Type

  • Hybrid
  • Regular

Experience Level

  • Senior Leader
  • 10+ years oncology drug development experience
  • 15+ years oncology drug development experience

Education Level

  • Advanced scientific or healthcare degree (PhD, PharmD)
  • Master’s Degree in life sciences

Salary/Compensations

  • $255,800.00 - $402,700.00

Benefits

  • Annual bonus and long-term incentive
  • Medical, dental, vision healthcare and other insurance benefits (for employee and family)
  • Retirement benefits, including 401(k)
  • Paid holidays, vacation, and compassionate and sick days

About the Company

  • Our company is committed to inclusion, ensuring that candidates can engage in a hiring process that exhibits their true capabilities.
  • We are proud to be a company that embraces the value of bringing together, talented, and committed people with diverse experiences, perspectives, skills and backgrounds.
  • The fastest way to breakthrough innovation is when people with diverse ideas, broad experiences, backgrounds, and skills come together in an inclusive environment.
  • We encourage our colleagues to respectfully challenge one another’s thinking and approach problems collectively.

Equal Opportunity

  • As an Equal Employment Opportunity Employer, we provide equal opportunities to all employees and applicants for employment and prohibit discrimination on the basis of race, color, age, religion, sex, sexual orientation, gender identity, national origin, protected veteran status, disability status, or other applicable legally protected characteristics.
  • As a federal contractor, we comply with all affirmative action requirements for protected veterans and individuals with disabilities.
  • For more information about personal rights under the U.S. Equal Opportunity Employment laws, visit: EEOC Know Your Rights
  • EEOC GINA Supplement
  • Learn more about your rights, including under California, Colorado and other US State Acts
  • San Francisco Residents Only: We will consider qualified applicants with arrest and conviction records for employment in compliance with the San Francisco Fair Chance Ordinance
  • Los Angeles Residents Only: We will consider for employment all qualified applicants, including those with criminal histories, in a manner consistent with the requirements of applicable state and local laws, including the City of Los Angeles’ Fair Chance Initiative for Hiring Ordinance