IQVIA

Senior Clinical Project Manager (Renal, Obesity, MASH) - Global Study Leadership - Poland

225.5k - 418.6k PLN225 500 - 418 600 PLN/ rok./ rok.UoPUmowa o pracę (brutto)

SeniorOn-site·WarszawaFull-time·Umowa o pracę

#401220·Dodano 3 miesiące temu·4

Źródło: IQVIA

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Tech Stack / Keywords

ICH-GCPclinical trialsproject managementrisk management

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. The Global Study Leadership team delivers clinical trials through therapeutically aligned and customer-dedicated delivery models, working on complex global clinical trials in therapeutic areas including Oncology, Rare Disease, CNS, Cardiovascular, Immunology, Respiratory, Renal, Obesity, MASH, Cell & Gene Therapy, Infectious Disease, Ophthalmology and Women's Health.

Wymagania

Bachelor's degree in Life Sciences, Healthcare, or related scientific discipline
7+ years clinical research experience including significant project management of global or multi-regional clinical trials in CRO, pharmaceutical, or biotechnology environment
Experience leading renal, obesity and/or MASH global clinical studies is strongly preferred
Strong knowledge of clinical trial conduct, ICH-GCP guidelines, and applicable regulatory requirements
Proven success leading cross-functional teams and managing study delivery (timelines, budgets, quality, risks, operational performance)
Ability to build trusted sponsor relationships and manage senior global stakeholders
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
Serve as the primary strategic partner for sponsors providing leadership 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
Ensure studies comply with ICH-GCP, regulatory requirements, and contractual commitments

Benefity

Opportunity to work on high-profile global studies
Collaboration with industry-leading sponsors
Leverage cutting-edge technology
Build a rewarding career with a leading clinical research organization

Inne informacje

IQVIA maintains a zero tolerance policy for candidate fraud. False statements, misrepresentations, or material omissions during recruitment will result in immediate application disqualification or employment termination according to applicable law.

IQVIA

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