Associate Principal, Strategic Lead

hace 2 semanas

Madrid, Madrid, España IQVIA A tiempo completo
About IQVIA

IQVIA is a leading global provider of advanced analytics, technology solutions, and clinical research services to the life sciences industry. Our mission is to push the boundaries of human science and data science to make a meaningful impact on the world.

Job Title: Associate Principal, Strategic

We are seeking an experienced Associate Principal to join our Patient-Centered Solutions team. As a key member of our team, you will be responsible for overseeing a portfolio of projects in the field of patient-centered research, developing and communicating strategic insights and recommendations to clients, and supporting business development.

Key Responsibilities:
  • Oversee and contribute to the delivery of a portfolio of consulting, scientific, and analytic projects
  • Develop and deliver insightful, value-added strategies that address complex client issues in the patient science field
  • Plan resources for project delivery, track, and ensure project financial health
  • Coach and direct project managers and project team members
  • Create reports, presentations, and facilitate workshops
  • Lead bid teams, develop proposals, and participate in business development processes
  • Develop a broad knowledge of patient science and how it addresses client needs for evidence generation and dissemination, regulatory, and market access strategy
  • Identify opportunities for expansion of PCS consulting service offerings
  • Support people-related activities such as recruitment, training, and development
  • Lead special initiatives that contribute to the growth and maturation of the PCS practice
Requirements:
  • An advanced academic science degree in public health, epidemiology, psychology, sociology, medical anthropology, health economics, or another related field
  • 5-8 years of experience in at least one of the above fields
  • Previous experience in strategic consulting and project management
  • Strong experience working in roles generating or communicating robust clinical data suitable for submission to regulatory bodies, payers, or for publication; preferably with exposure to COA/PRO, patient preference, and/or HEOR
  • Advanced knowledge of the healthcare regulatory processes and international payer systems
  • Ability to rapidly understand new scientific content and to engage meaningfully with clients and project teams
  • Excellent written and verbal communication skills, including presenting, facilitating meetings and workshops, and report writing
  • Demonstrable analytical, interpretative, and problem-solving skills
  • Excellent interpersonal skills and ability to work effectively with others
  • An ability to work in a fast-paced environment with demonstrated ability to effectively manage multiple tasks
  • An ability to establish and maintain effective working relationships in multi-disciplinary and international teams
What We Offer:
  • Become part of a recognized global leader in patient-focused research
  • Keep growing with an organization that encourages and invests in continuous professional and personal development
  • Develop your business and leadership skills further, with coaching from senior leaders
  • Continue challenging yourself by addressing the toughest client issues, working across multiple geographies and solutions in a dynamic and crucial field for the industry
  • Make a difference to patients by enabling the successful approval or launch of new treatments with features that are truly patient-centric

Please submit your CV in English.

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