Global Clinical Project Lead – Senior CPM

iqvia; Warszawa; On-site; PLN 218,000 - 405,000; Full time

Job summary

IQVIA Biotech in Poland is seeking an experienced CPM/Sr CPM to lead regional/global clinical trials in cardiovascular, renal, or metabolic areas. You will ensure delivery per contract, optimize speed, quality and cost, and collaborate with cross-functional teams across geographies.

This role requires at least 4 years of CPM experience, strong knowledge of ICH GCP, and excellent English communication. Occasional travel to the United States may be required.

Qualifications

• Bachelor’s degree in life sciences or related field.
• 5 years of CPM experience with >1 year PM experience.
• Knowledge of ICH GCP and local regulations.
• Strong English communication skills.
• Experience with cardiovascular/metabolic trials is a plus.

Responsibilities

• Lead execution of clinical studies per contract while optimizing speed, quality and cost.
• Set objectives for the core project team and assess performance.
• Participate in bid defenses and may lead regional studies.
• Develop integrated study management plans with the core project team.
• Monitor progress and manage risks and contingencies.
• Ensure financial success and report to stakeholders.

Skills

Project management

Life sciences background

GCP/regulatory knowledge

English communication

Cross-functional collaboration

Education

Bachelor's degree Life sciences or related field

Job description

IQVIA Biotech in Poland is seeking an experienced CPM/Sr CPM to lead regional/global clinical trials in cardiovascular, renal, or metabolic areas. You will ensure delivery per contract, optimize speed, quality and cost, and collaborate with cross-functional teams across geographies.

This role requires at least 4 years of CPM experience, strong knowledge of ICH GCP, and excellent English communication. Occasional travel to the United States may be required.