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    Senior Director, BPM Evidence Platforms - Warsaw, Polska - AstraZeneca

    AstraZeneca
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    W pełnym wymiarze godzin
    Opis

    Biopharmaceuticals Medical (BPM) ensures the best patient outcomes by providing healthcare decision-makers around the world with the evidence and confidence they need on AZ therapies and support our internal stakeholders with medical insight and expertise. BPM provides medical leadership with market participation and connectivity while also impacting the life cycle planning and execution of all our products. Global Medical Affairs aims to lead AstraZeneca in achieving scientific leadership, being a great place to work, and keeping patients at the core of everything we do.

    The BPM Medical Evidence organization is accountable for the delivery of global strategic studies required to generate the evidence to build the confidence on AZ therapies and additional observational, interventional and externally sponsored research required by Global Product Teams and Global Medical Teams.

    As head of the Medical Evidence Enablement Team, the Senior Director of BPM Evidence Platforms develops technical strategies and processes needed to drive Evidence generation at the local, regional and global levels. This role will be accountable for driving the system roadmap and strategy for all Medical Evidence owned technology platforms, enterprise interfaces (e.g., VCV/ACCORD /PLANIT/) and tools. In addition, you will assess and translate new business needs into pragmatic and efficient business processes, tools and technology platforms to enable evidence delivery within BioPharmaceuticals and Oncology Business Units, and regional and local market evidence teams.

    The key areas of focus for the Senior Director, Evidence Enablement will include

  • Lead planning efforts to define and execute the long-range Evidence system strategy across all Therapeutic Area Evidence Teams
  • Work closely with Senior Leadership, Therapeutic Area Evidence Head(s), and critical business functional areas to ensure alignment of system strategy to delivery operating procedures.
  • Drive efficient operation of the Evidence Enablement team (including overall plans, priorities and risk management).
  • Drive communication strategy and alignment of systems strategy to standard operating procedures in support of global, regional and local Evidence delivery teams
  • Represent Medical Evidence needs and requirements to external AstraZeneca wide programs such as the Digital Health Platform; working to ensure Medical Evidence can leverage organizational systems.
  • Drive strategic direction of Evidence Explorer to ensure that RWE groups across AstraZeneca and within the local markets to achieve the desired cost savings.
  • This role requires a hybrid skill set of technical ability, business acumen, and knowledge of evidence generation.

    Tools and technology platforms supported by this role include, but are not limited to, Evidence Connect, Evidence Explorer, DataVision/Clear, SharePoint Online and macro-enabled excel tools.

    Typical Accountabilities

  • Ensure organizational awareness of Evidence Delivery processes and needs; supporting alignment of cross-organizational systems such as the Evidence Explorer and Veeva Clinical Vault CTMS
  • Manage senior, global cross-functional team meetings and action items
  • Manage the cross-functional Medical Evidence system roadmap plan and timelines and formulates the project scope, project plan, critical paths and risk-mitigation strategies across the Evidence teams.
  • Work with Global, Regional and Local Evidence teams and RWE groups to define and communicate Evidence system strategy and needs
  • Work across Therapeutic Areas and enterprise-wide functional areas (e.g., Patient Safety, Publications, RWE, Patient Centered Science) to ensure alignment where possible between BPM and OBU evidence system strategies
  • Act as member of Digital Health Platform change control boards to ensure Evidence systems strategy is considered as changes are evaluated
  • Coach Enablement project teams towards successful issue resolution and decision making and focus the team on the right activities at the right time.
  • Communicate Medical Evidence system needs and strategy to key stakeholders
  • Manage the Medical Enablement budget
  • Liaise with IT and other systems owners to develop long term relationships for Medical Evidence inclusion
  • Coordinate and participate in activities that ensure Medical Evidence compliance and license to operate (e.g. legal hold); contribute to activities in support of audits
  • Manage the identification and escalation of potential issues/risks or obstacles to strategic roadmap and achieve resolution or plan contingencies and follow issues through to resolution ensuring that all issues arrive at a singular conclusion or recommendation.
  • Establish, communicate and execute global plans that drive toward goal achievement.
  • Essential

  • Ability to motivate, lead and inspire high performing teams
  • Strong people leadership and ability to function collaboratively in a matrix environment with appropriate influencing, networking and stakeholder management skills; including the ability to manage up
  • Experienced project manager with successful track record of project delivery within agreed time, quality and cost
  • BA/BS in a Science or Health related discipline or equivalent experience
  • Proven experience independently managing or leading cross-functional project teams in a complex pharmaceutical multi-disciplinary, global oncology environment
  • 7-10 years' plus demonstrated success in leading projects in a structured and organized manner
  • Proven leadership experience in managing a global, cross-functional matrix teams with demonstrated skills in strategic planning, risk mitigation, and operation problem solving
  • Ability to effectively manage multiple diverse cross-functional teams in a matrix organizational structure
  • Excellent verbal, written, and organizational communication skills
  • Strategic mindset
  • High attention to detail
  • Strong work ethics and high integrity standards
  • Good organizational and project Management skills and experience; Proactively identifies risks and issues and possible solutions; Demonstrate ability to follow tasks through to completion
  • Demonstrated ability to interrogate, understand and apply project management data
  • High level knowledge/awareness of the overall pharmaceutical product development process, including stages of development and role of different functional areas.
  • Desirable

  • MA/MS/PhD; MBA, RPH, PharmD is a plus
  • Deep knowledge of the Medical Evidence delivery study types, systems and delivery processes
  • Proficient with project management tools
  • Date Posted

    12-Apr-2024

    Closing Date

    30-Apr-2024


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