CPM
On-site · Frankfurt am Main, Hesse, Germany
Job Summary
Clinical Project Lead responsible for delivering clinical studies to meet contract requirements, leveraging IQVIA solutions to drive operational excellence. Core duties include developing integrated study management plans, ensuring timely and cost-efficient delivery, managing cross-functional teams and stakeholder communications, leading bid defense presentations, monitoring progress and risks, and maintaining quality and contract compliance across studies. The role requires life sciences education, strong leadership and communication skills, and knowledge of ICH GCP and regulatory requirements; proficiency with MS Office and ability to collaborate with customers and vendors to accelerate study delivery.
Required Qualifications
- Bachelor's Degree Life sciences or related field
- 5 years of prior relevant experience including > 1 years project management experience or equivalent combination of education, training and experience
- Knowledge of clinical trials - Knowledge of clinical trial conduct, and skill in applying applicable clinical research regulatory requirements i.e. ICH GCP and relevant local laws, regulations and guidelines, towards clinical trial conduct
- Strong written and verbal communication skills including good command of English language
- Strong presentation skills
- Problem solving - Strong problem solving skills
- Leadership - Ability to work through others to deliver results to the appropriate quality and timeline metrics
- Planning, time management and prioritization skills
- Quality - Attention to detail and accuracy in work
- IQVIA Core Competencies - Client Focus, Collaboration, Communication, innovation, Ownership
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