Wróć do listy

Opis oferty

Associate Program Director, Regulatory Affairs w Warszawa, Polska

IQVIA

Warszawa, Polska

IQVIA seeks an Associate Program Director for Regulatory Affairs to lead complex global regulatory programs for pharmaceutical and biotechnology clients. This strategic role oversees multiple workstreams, manages senior client relationships, and drives program governance and financial performance across the product development lifecycle.

Responsibilities

  • Lead complex global Regulatory Affairs programs across multiple projects and functional teams
  • Serve as strategic senior contact for clients and manage executive-level stakeholder relationships
  • Establish program governance, oversight plans, KPIs and establish delivery frameworks
  • Oversee cross-functional regulatory teams spanning strategy, operations, submissions and lifecycle management
  • Monitor program performance, profitability and revenue realization with corrective action as needed

Requirements

  • Bachelor's degree in Life Sciences, Pharmacy, Regulatory Affairs or related field
  • Significant experience in Regulatory Affairs, Operations, or Strategy within CRO, pharma or biotech
  • Proven track record leading large, complex global programs or portfolios
  • Strong understanding of global regulatory frameworks and drug development processes
  • Professional fluency in English and French, including client meeting leadership
  • Experience managing client budgets, revenue forecasts and resource planning
  • PMP, PRINCE2 or equivalent project management certification advantageous
Aplikuj na ofertę

Podobne oferty

Więcej podobnych stanowisk

NATEK POLAND

Associate Director, Regulatory Processes

  • Zdalnie
  • Kontrakt
Twój zakres obowiązków - Zarządzanie przypisanymi procesami i projektami regulacyjnymi, w tym ich wdrażaniem, monitorowaniem, komunikacją i zapewnieniem zgodności. - Współpraca z właścicielami procesów i ekspertami regulacyjnymi przy opracowywaniu, monitorowaniu, raportowaniu i ocenie globalnych wskaźników KPI.

Warszawa, Polska

Bristol Myers Squibb

Associate Director, Program Management

  • Zarzadzanie projektami
Bristol Myers Squibb seeks an Associate Director of Program Management to partner with global leadership in overseeing strategic and operational planning for drug development programs. The role combines cross-functional team coordination with independent oversight of moderate-complexity early and late-stage development ...

Warszawa, Polska

QbD Group

Senior Consultant Regulatory Affairs

  • Hybrydowo
  • Pełny etat
  • Doradztwo
Location : Hybrid - Madrid or Warsaw Type : Full-time We are looking for an experienced Regulatory Affairs professional to join our growing team and play a key role in delivering regulatory services to our clients across European markets. This position offers the opportunity to manage complex regulatory projects, advise ...

Warszawa, Polska

Stada Poland Sp. z o.o.

Medical & Regulatory Affairs Junior Manager

Medical & Regulatory Affairs Junior Manager Your responsibilities - Coordination, preparation and review regulatory submissions for national and European procedures - Ensure compliance with regulatory standards and guidelines - Interaction with regulatory agencies to expedite approval of pending registrations - Management ...

Warszawa, Polska

Ergomed

Study Start Up and Regulatory Affairs Specialist

... cares about the people behind the work as much as the work itself, we would love to hear from you. Job Description The Specialist, Study Start Up and Regulatory Affairs leads and coordinates all activities related to achieving site initiation readiness. The role provides subject matter expertise, ensures regulatory compliance, ...

Kraków, Polska

Ergomed

Study Start Up and Regulatory Affairs Specialist

... a team that cares about the people behind the work as much as the work itself, we would love to hear from you. The Specialist, Study Start Up and Regulatory Affairs leads and coordinates all activities related to achieving site initiation readiness. The role provides subject matter expertise, ensures regulatory compliance, ...

Polska

TANTUS Sp. z o.o.

Specjalista / Specjalistka ds. Zapewnienia Jakości i Regulacji (Regulatory Affairs)

Specjalista / Specjalistka ds. Zapewnienia Jakości i Regulacji (Regulatory Affairs) Miejsce pracy: Pruszków Twój zakres obowiązków - Nadzór nad dokumentacją produktową suplementów diety, w tym opracowywanie i zatwierdzanie specyfikacji - Zapewnienie zgodności wyrobów z wymaganiami prawa żywnościowego - Weryfikacja znakowania ...

Pruszków, Polska

IQVIA

Associate Program Director, Regulatory Affairs

  • Część etatu

220800 - 469400 zł / rocznie

... and commercialization of innovative therapies that improve patient outcomes worldwide. We are seeking an experienced Associate Program Director, Regulatory Affairs to join our Global Regulatory Affairs team in Eastern Europe. In this strategic client-facing role, you will lead complex global regulatory programs for pharmaceutical, ...

Warszawa, Polska

McCormick & Company

McCormick SSC - Talent Pipeline for Food Regulatory Compliance Analysts (m/f)

  • Zdalnie
  • Zgodnosc
... passionate about food legislation, regulatory affairs, product compliance, and food quality , join our talent pipeline for future opportunities within the Food Regulatory Compliance area. If you have education or experience in fields such as: - Food Technology - Food Science - Nutrition - Regulatory Affairs - Quality Assurance ...

Łódź, Polska

IQVIA

Associate Director - Operational Effectiveness

Associate Director – Operational Effectiveness Job Overview Lead complex, highly visible, global AI-enabled transformation initiatives that accelerate operational excellence, productivity, and value realization across the enterprise. This role drives the design and execution of AI transformation initiatives and enables ...

Warszawa, Polska