Senior Oncology Clinical Project Lead

IQVIA Argentina

Warszawa

On-site

PLN 180,000 - 300,000

Full time

8 days ago
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Job summary

IQVIA Biotech is recruiting an experienced CPM/Sr CPM to join our established team in Warsaw. The successful candidate will manage regional/global clinical trials, with a strong focus on oncology, applying IQVIA solutions to deliver on-time, within-budget study delivery.

This role requires at least four years of CPM experience, solid leadership and communication skills, and the ability to work cross-functionally across geographies.

Qualifications

  • Bachelor's Degree in Life sciences or related field.
  • 4+ years CPM experience with regional/global exposure.
  • Strong knowledge of oncology trials and regulatory requirements (ICH GCP).
  • Excellent written and verbal English communication.

Responsibilities

  • Accountable for execution of clinical studies or assigned portion, ensuring speed, quality and cost efficiency.
  • Set objectives for core project team and assess performance.
  • Participate in bid defense presentations and lead for smaller regional studies.
  • Develop integrated study management plans with the core project team.
  • Collaborate with other functional groups to support milestones and resolve issues.
  • Monitor progress and prepare project information for stakeholders.
  • Manage risks and contingencies, driving problem solving and corrective actions.
  • Serve as primary or backup project contact with customers and IQVIA BD partners.
  • Lead cross-functional team efforts to deliver on milestones and study objectives.
  • Ensure financial success of the project and forecast opportunities to accelerate revenue.

Skills

Communication skills
CPM experience
Oncology trial experience
Leadership
Cross-functional collaboration

Education

Bachelor's Degree Life sciences or related field

Job description

IQVIA Biotech is recruiting an experienced CPM/Sr CPM to join our established team in Warsaw. The successful candidate will manage regional/global clinical trials, with a strong focus on oncology, applying IQVIA solutions to deliver on-time, within-budget study delivery.

This role requires at least four years of CPM experience, solid leadership and communication skills, and the ability to work cross-functionally across geographies.

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