ViatrisVI

Global Program Lead

Viatris

Salary: 225k-350k USD

United States only
Apply now
Mylan Inc.

At VIATRIS, we see healthcare not as it is but as it should be. We act courageously and are uniquely positioned to be a source of stability in a world of evolving healthcare needs.

Viatris empowers people worldwide to live healthier at every stage of life.

We do so via:

  • Access – Providing high quality trusted medicines regardless of geography or circumstance;

  • Leadership – Advancing sustainable operations and innovative solutions to improve patient health; and

  • Partnership – Leveraging our collective expertise to connect people to products and services.

Every day, we rise to the challenge to make a difference and here’s how the Global Program Lead role will make an impact:

Key responsibilities for this role include:

  • The Global Program lead (GPL) manages one or more development program(s) of one or more drug candidate by leading multidisciplinary/cross-functional team(s) from relevant expert functions, as part of the company's strategy.

  • The GPL is responsible for leading the creation and delivery of an integrated asset strategy throughout the lifecycle maximizing the value of the asset/program(s) or group of programs.

  • The GPL is responsible for leading the program and program team to achieve the objectives in accordance with quality standards and within timelines validated with the Development Committee.

  • The GPL ensures oversight of the Program budget and are accountable for ensuring delivery of project according to quality, time, program budget and resources.

  • The GPL Is responsible for ensuring that all activities related to the program(s) are conducted within the framework of the agreed asset strategy, and with cross-functional alignment of all functions involved in the drug development process.

  • At all phases of planning and implementation, the PTL ensures appropriate validation by and reporting to the Development Committee according to company processes.

  • The GPL is responsible for:

    • Program strategy, planning and execution.

    • Owning the integrated strategy for the asset.

    • Defining and delivering the integrated program development plan by coordinating all key functions.

    • Ensuring the validation of integrated development plan by key stakeholders.

    • Ensuring cross-functional engagement / way of working to ensure full team alignment and utilizing every member of the team to execute the program strategy.

  • Responsible for the robust assessment of opportunities, risks, in conjunction with the key function leaders, in order to maximize value of the asset/program.

  • Responsible to set up backup scenarios, as well as « go/no go decision points » to mitigate risks and to present them to Governance meetings. Develops and recommends strategic options to governance.

  • Drives implementation of the plans whilst managing risks. Oversees the program budget and ensure it fits with the strategic needs and agreed roadmap in conjunction with finance and expert functions.

  • Responsible for appropriate internal communication to Program team and stakeholders. Contributes to and adopts relevant aspects of the company’s portfolio management process.

  • The GPL engages in regular, competent and active communication with key stakeholders as a representative of the company both internally and externally (congress, partnering, and negotiation).

  • The GPL is responsible for defining & implementing Program internal & external communication plans:

    • Proposing and conducting communications concerning the results of both scientific and clinical studies in association with the cross-functional team.

    • Ensuring consistency across Program messages for external communication.

  • Performs other duties as assigned.

Here are the minimum qualifications for this position:

  • Advanced Scientific degree or strong demonstration of equivalent combination of relevant educational and professional training experience in leading cross-functional teams.

  • Strong understanding of Regulatory requirements from a Drug Safety and Quality perspective.

  • 10+ years proven experience in the Biotechnology, Pharmaceutical, or other Healthcare-related field as a Program Leader or equivalent.

  • Drug Development knowledge with solid understanding of other functions relevant to the position which may include Preclinical, Clinical, QA, Drug Safety, Manufacturing, Commercial and Regulatory.

  • Proven track record to advance pharmaceutical products through the pipeline. A thorough knowledge of the pharmaceutical business model, of the value chain, especially in a Health Care environment.

  • Independent, motivated, team member with the ability to thrive in a matrix environment.

  • Superb written and verbal communication. Strong interpersonal skills with the ability to communicate with all levels of management through diplomacy and tact.

  • Ability to influence others and move toward a common vision or goal.

Exact compensation may vary based on skills, experience, and location. The salary range for this position is $225,000.00 to $350,000.00 USD.

At Viatris, we offer competitive salaries, benefits and an inclusive environment where you can use your experiences, perspectives and skills to help make an impact on the lives of others.

Viatris is an Equal Opportunity Employer. All qualified applicants will receive consideration for employment without regard to race, national origin, religion, age, color, sex, sexual orientation, gender identity, gender expression, disability, or protected veteran status, or any other characteristic protected by local, state, or federal laws, rules, or regulations.

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About the job

Apply before

Aug 26, 2024

Posted on

Jun 27, 2024

Job type

Full Time

Experience level

Senior

Salary

Salary: 225k-350k USD

Location requirements

Hiring timezones

United States +/- 0 hours
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