Senior Clinical Project Manager - CVRM Trials

IQVIA LLC; Warszawa; Presencial; PLN 218.000 - 405.000; Jornada completa

Descripción de la vacante

IQVIA Biotech is seeking an experienced CPM/Sr CPM to join our established team in Warszawa. You will manage regional/global studies, lead core project teams, and drive delivery with a focus on quality, timelines, and budget.

A minimum of 4 years CPM experience in cardiovascular, renal, or metabolic trials is required. The role involves collaboration across functions, risk management, and keeping customers informed with proactive communication.

Formación

• Bachelor's degree in life sciences or related field.
• 5+ years CPM experience including 1+ year in project management.
• Knowledge of clinical trial conduct and ICH GCP requirements.
• Therapeutic area knowledge in cardiovascular/metabolic/renal is advantageous.
• Strong communication and cross-functional collaboration skills.

Responsabilidades

• Execute clinical studies or portions per contract, optimizing speed, quality and cost.
• Set objectives for core project team and assess performance.
• Lead bid defense presentations with Business Development for regional studies.
• Deliver and manage smaller regional studies as needed.
• Develop integrated study management plans with core team.

Conocimientos

Project management

Cross-functional collaboration

Client/stakeholder communication

Decision making

Planning & prioritization

Educación

Bachelor's Degree Life sciences or related field

Herramientas

Software & computer skills

Descripción del empleo

IQVIA Biotech is seeking an experienced CPM/Sr CPM to join our established team in Warszawa. You will manage regional/global studies, lead core project teams, and drive delivery with a focus on quality, timelines, and budget.

A minimum of 4 years CPM experience in cardiovascular, renal, or metabolic trials is required. The role involves collaboration across functions, risk management, and keeping customers informed with proactive communication.