Associate Director, Global Integrated Evidence Operations

Otsuka Pharmaceutical Co., Ltd.Princeton, NJ
7d$164,530 - $245,985

About The Position

Summary: The Global Integrated Evidence Operations, Associate Director role oversees and coordinates the operational processes, digital system support, and governance for Global Integrated Evidence & Innovation (GIE&I), which includes responsibility for operating models, system readiness, and process adherence for integrated evidence planning (IEP) and generation programs across the enterprise. In addition, the role will play a crucial role in enhancing the efficiency and effectiveness of general department operations to support timely and transparent delivery of high impact evidence.

Requirements

  • Bachelor's degree in drug development or business management.
  • 5+ years of experience in life sciences or project management supporting research needs.
  • Proven track record in program management with matrixed teams in health or life sciences.
  • Strategic mindset with the ability to prioritize tasks and focus work accordingly.
  • Capability to synthesize large amounts of data into meaningful content.
  • Strong written, verbal, and presentation skills for diverse stakeholders.
  • Excellent project, time management, and organizational skills.
  • Ability to thrive under pressure, meet deadlines, and lead parallel projects.
  • Competence in drug development lifecycle and scientific understanding of assets.
  • Accountability for Results - Stay focused on key strategic objectives, be accountable for high standards of performance, and take an active role in leading change.
  • Strategic Thinking & Problem Solving - Make decisions considering the long-term impact to customers, patients, employees, and the business.
  • Patient & Customer Centricity - Maintain an ongoing focus on the needs of our customers and/or key stakeholders.
  • Impactful Communication - Communicate with logic, clarity, and respect. Influence at all levels to achieve the best results for Otsuka.
  • Respectful Collaboration - Seek and value others’ perspectives and strive for diverse partnerships to enhance work toward common goals.
  • Empowered Development - Play an active role in professional development as a business imperative.

Nice To Haves

  • Formal training or certification in project management methodologies (PMP, Six Sigma, Agile).
  • Experience in developing IEPs or managing complex processes across cross-functional stakeholders.
  • Experience in leading or working closely with leadership governance
  • Successful execution and management of multiple projects supporting life sciences research.
  • Technical experience in drug development/commercialization.
  • Knowledge of drug development lifecycle functions such as Discovery, Clinical Trials, and Regulatory.
  • Experience with digital technology to support management of planning and research

Responsibilities

  • Support the creation and management of IEP program with a focus on operational efficiency by building out and maintaining digital planning platform/repository
  • Track and report IEP program updates to leadership
  • Oversee the digital IEP planning platform/repository and monitor data quality
  • Ensure operational excellence through the continued development and implementation of standardized processes, tools, and governance for IEP and generation
  • Contribute to the development of operational KPIs and dashboards to monitor performance and drive continuous improvement for IEP planning and generation
  • Lead enterprise training, change management, and capability building for systems, process, and governance
  • Support evidence planning governance to ensure alignment with asset vision and strategic objectives
  • Support evidence generation governance to oversee the execution of evidence generation activities.
  • Contribute strategic thinking and thought partnership for evidence operations, systems and governance
  • Recommend process improvements and efficiencies to leadership
  • Develop and maintain relationships with colleagues involved in the IEP, evidence generation and governance processes.

Benefits

  • Comprehensive medical, dental, vision, prescription drug coverage, company provided basic life, accidental death & dismemberment, short-term and long-term disability insurance, tuition reimbursement, student loan assistance, a generous 401(k) match, flexible time off, paid holidays, and paid leave programs as well as other company provided benefits.

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What This Job Offers

Job Type

Full-time

Career Level

Mid Level

Number of Employees

1,001-5,000 employees

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