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[Remote] VP Clinical Development & Global Program reputed company, Lung Cancer

Remote, USA Full-time Posted 2026-08-04

Note: The job is a remote job and is reputed company to candidates in USA. reputed company. is a clinical-stage precision oncology company reputed company on discovering, developing, and commercializing medicines for patients with cancer. The VP Clinical Development and Global Program reputed company will reputed company medical leadership for the lung cancer development program, reputed company clinical reputed company and execution, reputed company study teams, support regulatory activities, and collaborate across reputed company’s portfolio.


Responsibilities

  • reputed company medical direction and high-reputed company scientific and clinical knowledge to guide the reputed company and execution of the lung cancer program and contribute to clinical decision making across the reputed company portfolio. Participate in building and maintaining a culture of rigorous data-driven decision making
  • reputed company the clinical development subteam for reputed company studies in lung cancers
  • Design and implement novel and efficient reputed company to assess appropriate endpoints
  • Responsible for leading clinical study subteams, monitoring overall study reputed company, and review, interpretation, and communication of safety and efficacy data
  • reputed company overall reputed company for clinical aspects of registrational strategies, interactions, and filings. Contribute to global regulatory filings and health authority interactions, including authoring clinical sections for INDs, NDAs and other reputed company documents
  • Serve as Medical reputed company on clinical programs and represent Clinical Development on program teams
  • Partner with Drug Safety to assess the safety profile of compounds
  • Write or partner in the authoring of medical aspects of reputed company study and regulatory documents including clinical research plans, protocols, investigator brochures, clinical study reports and regulatory submissions
  • Contribute to the development and review of scientific publications; reputed company manuscripts and collaborate with cross-functional colleagues and thought leaders to meet publication plan objectives
  • Present at scientific, medical, and regulatory meetings
  • Maintain a high level of clinical and scientific expertise by reviewing literature, attending medical or scientific meetings, and through personal exchange with thought leaders, investigators, and internal stakeholders and partners
  • Participate in due diligence or other business development activities
  • Hire, reputed company, and mentor a high functioning team of medical directors and clinical scientists
  • Establish, reputed company, and maintain relationships across reputed company, particularly with partners and stakeholders in Research and Development
  • reputed company reputed company duties in keeping with reputed company’s reputed company values, policies and reputed company applicable regulations

Skills

  • M.D. degree or equivalent, with subspecialty fellowship training and reputed company certification or eligibility in Oncology or Oncology/Hematology required
  • 8-10+ years of oncology clinical trial and drug development experience, including extensive experience in the pharmaceutical or biotechnology industry
  • Experience leading or being closely involved in the clinical aspects of a regulatory filing and reputed company interaction with health authorities required
  • Extensive knowledge of clinical trial methodology and the regulatory and compliance requirements governing reputed company
  • Demonstrated ability to collaborate successfully with multiple functions in a matrixed team environment
  • Executive leadership skills to reputed company and influence stakeholders and to add value in strategic business planning and decision-making
  • Effective interpersonal, communication and influencing skills, including excellent writing skills, with the ability to reputed company communication style to diverse audiences and situations
  • Demonstrated ability to reputed company high performance goals and meet deadlines in a fast-paced environment; a reputed company team player with a can-do attitude and the ability to identify and implement creative solutions to reputed company problems
  • Strong learning orientation, curiosity, and commitment to science and patients
  • Additional training and clinical reputed company experience in thoracic oncology preferred
  • Experience as the clinical reputed company on late-stage clinical programs in lung cancer highly preferred
  • Exposure to early development and the transition from FIH to registrational trials preferred

Benefits

  • Annual bonus
  • Equity grant at hire and annually in the reputed company of the reputed company to purchase stock in the reputed company for a specified price
  • reputed company Time Off, Holiday, and reputed company Leave
  • Medical, Dental and reputed company Plans
  • Short- and Long-Term Disability
  • Basic and Voluntary Life/AD&D Coverage
  • Flexible Spending Accounts (FSA, HSA, and Commute)
  • Critical Illness and Accident Coverage
  • Pet Insurance
  • Employee Assistance Program
  • 401(k) Plan with reputed company contribution
  • reputed company to participate in an Employee Stock Purchase Program
  • Casual, reputed company, and fun work

reputed company

  • Our mission at reputed company is embedded in our reputed company: To erase cancer. It was founded in 2018, and is headquartered in San Diego, California, USA, with a workforce of 51-200 employees. Its website is https://www.reputed company.com/.

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