Teva Sr Manager Patient Centered Development 

United States, Pennsylvania, East Bradford Township 

507782510

The Manager, Patient-Centered Development is responsible to support early planning initiatives, evaluation, and implementation of patient centered activities within clinical development programs and clinical trials within Global Clinical Operations Innovative and Biosimilars. This role will include creating, optimizing and revising processes related to patient-centered development and activities, managing cross-functional activities related to patient advocacy organizations and patient engagement. This role will support the creation and execution of activities related to the Diversity Action Plans associated initiatives both centrally and on a project-specific level. In addition, manage early project initiatives, such as recruitment strategies from start to implementation may be required.

Travel Requirements: As required, up to 20%

Essential Duties & Responsibilities:

• Lead the creation, maintenance and updates of processes and template related to patient-centered development, including but not limited to the Diversity Action Plan and raising awareness of Diversity and Inclusion strategies in clinical trials within the organization.
• Engage Patient Advocacy Organizations to cultivate relationships and leverage them to conduct patient engagement initiatives related to programs and/or studies. Plan and execute associated projects and communication progress and feedback to cross-functional team.
• Support Director of TOP with overall strategy to operationalize activities related to the Diversity plans and Patient Insights in a creative, innovative and efficient way.
• Work with TOP lead to initiate, develop and implement new methodologies related to tracking metrics and reporting metrics relative to internal KPIs and industry benchmark, as available
• Work as part of a global, professional and cross-functional team
• Resolve and/or escalate issues in a timely fashion.
• Ensure timely, efficient and high-quality deliverables in all projects.
  

Requirements:

• Bachelors or higher degree in Science, Industrial Engineering, or equivalent combination of education and related work experience
• Minimum of 3 years' experience as a project manager in patient engagement, clinical trial planning/feasibility departments, or equivalent in other sponsors, CRO or relevant vendors.
• Knowledge of standard Windows programs (Word, Power Point, Outlook etc.).
• Ability to effectively interact with and influence others without direct reporting relationships

Preferred:

• Experience in setting new methodologies and processes in clinical trials related organizations
• ICH-GCP
• Specialized or Technical Knowledge Licenses, Certifications needed: Not applicable
• Functional Knowledge: A proven knowledge in clinical studies and clinical development processes
• Company/Industry Related Knowledge: Understanding of clinical trial data and pharmaceutical development

Job-Specific Competencies:

• Strong written and verbal English
• Strong resource management and project management skills
• Critical thinking and strong analytical and problem-solving skills
• Strong interpersonal and communication skills
• Ability to work as a part of a global team and independently
• Strong organizational skills with ability to manage multiple project initiatives simultaneously
• Ability to work in a global changing environment
• Strong technology orientation
• Good understanding of the service supplier industry
• Initiative, diligence, dedication, independent, hands-on
• Ability to work under pressure and multi-task
  

We offer a competitive benefits package, including:

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