Associate Principal, Strategic Lead

hace 2 días


Madrid, Madrid, España IQVIA A tiempo completo

IQVIA is a leading global provider of advanced analytics, technology solutions, and clinical research services to the life sciences industry.

We are seeking an Associate Principal to join our Patient-Centered Solutions team, where you will oversee a portfolio of projects in the field of patient-centred research.

As an Associate Principal, you will be responsible for developing and communicating strategic insights and recommendations to clients, and for supporting business development.

Key responsibilities include:

  • Overseeing and contributing to delivery of a portfolio of consulting, scientific, and analytic projects
  • Developing and delivering insightful, value-added strategies that address complex client issues in the patient science field
  • Planning resources for project delivery, tracking, and ensuring project financial health
  • Coaching and directing project managers and project team members
  • Creating reports, presentations, and facilitating workshops
  • Leading bid teams, developing proposals, and participating in business development processes
  • Developing a broad knowledge of patient science and how it addresses client needs for evidence generation and dissemination, regulatory, and market access strategy
  • Identifying opportunities for expansion of PCS consulting service offerings
  • Supporting people-related activities such as recruitment, training, and development
  • Leading special initiatives that contribute to the growth and maturing of the PCS practice

Essential experience, skills, and education required include:

  • 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

Please submit your CV in English.



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