Senior CPM for Cardiovascular & Metabolic Trials

IQVIA

Warszawa

On-site

PLN 218,000 - 405,000

Full time

4 days ago

Be an early applicant

Application generator

Stand out for this role — generate a tailored resume and cover letter in about a minute.

Get past ATS filters

Job summary

IQVIA Biotech is seeking an experienced CPM/Sr CPM to join our established team in managing cardiovascular, renal or metabolic trials. A minimum of 4 years regional/global CPM experience is required, with strong regulatory and clinical trial know-how.

The role focuses on project delivery, quality and financial performance, leading cross-functional study teams and collaborating with IQVIA's global clients to drive operational excellence across all phases.

Qualifications

Bachelor's degree in life sciences or related field.
Minimum 4 years regional/global CPM experience.
Experience in cardiovascular, renal, or metabolic trials preferred.
Knowledge of ICH GCP and local regulations.
Strong communication and English proficiency.

Responsibilities

Oversee execution of clinical studies per contract, optimizing speed, quality and cost.
Set objectives for core project team and assess performance.
Lead bid defenses with Business Development for regional studies.
Develop integrated study management plans.
Collaborate with cross-functional teams to meet milestones.
Monitor progress and manage risks and issues.
Ensure project financials and forecast opportunities.
Provide input on team performance and staff development.