IQVIA
IQVIA
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Senior Clinical Project Manager - Global Study Leadership (Poland)

225.5k - 418.6k PLN/ rok.UoP
SeniorFull-time·Umowa o pracę
#393666·Dodano 4 dni temu·1
Źródło: IQVIA
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Tech Stack / Keywords

ICH-GCPClinical TrialsLife SciencesHealthcareClinical ResearchCRORegulatory Requirements

Firma i stanowisko

IQVIA is a leading global provider of clinical research services, commercial insights and healthcare intelligence to the life sciences and healthcare industries. It specializes in delivering clinical trials through therapeutically aligned and customer-dedicated delivery models for pharmaceutical and biotechnology companies.

Wymagania

  • Bachelor's degree in Life Sciences, Healthcare, or related scientific discipline
  • 7+ years clinical research experience with significant project management of global or multi-regional clinical trials in CRO, pharmaceutical, or biotechnology environments
  • Strong knowledge of clinical trial conduct, ICH-GCP guidelines, and regulatory requirements
  • Proven success leading cross-functional teams and managing study delivery (timelines, budgets, quality, risks, operations)
  • Ability to build trusted sponsor relationships and manage senior stakeholders globally
  • Exceptional leadership, communication, problem-solving, and decision-making skills
  • Passion for advancing clinical research and improving patient outcomes

Obowiązki

  • Lead delivery of complex global and multi-regional clinical studies, ensuring operational excellence and successful outcomes
  • Serve as primary strategic partner for sponsors, providing leadership, guidance, and innovative solutions
  • Provide leadership and direction to cross-functional teams across regions
  • Oversee study timelines, budgets, quality, risks, financial performance, and operational delivery
  • Drive proactive risk management, issue resolution, decision-making, and stakeholder alignment throughout the study lifecycle
  • Ensure study compliance with ICH-GCP, regulatory requirements, and contractual commitments

Benefity

  • Opportunity to work on high-profile global studies
  • Collaboration with industry-leading sponsors
  • Access to cutting-edge technology and data-driven insights
  • Career development within a leading clinical research organization
  • Potential incentive plans, bonuses, and comprehensive health and welfare benefits
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Inne informacje

IQVIA maintains a zero tolerance policy for candidate fraud. False statements, misrepresentations, or omissions during recruitment will result in disqualification or termination in accordance with law.

IQVIA

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