ProPharma partners with biotech, med device, and pharmaceutical organizations to advance scientific breakthroughs and introduce new therapies through a comprehensive advise-build-operate model
Job Summary
ProPharma partners with biotech, med device, and pharmaceutical organizations to advance scientific breakthroughs and introduce new therapies through a comprehensive advise-build-operate model.
The Clinical Project Manager will lead and deliver clinical studies across Europe, ensuring timelines, quality, and compliance standards are consistently met.
ProPharma is committed to diversity, equity, and inclusion, providing a safe and empowering workplace where employees can be their authentic selves.
Matching Summary
ProPharma partners with biotech, med device, and pharmaceutical organizations to advance scientific breakthroughs and introduce new therapies through a comprehensive advise-build-operate model.
Skills & Requirements
Must-have
Clinical trial execution and delivery
Regulatory compliance and quality standards
Cross-functional team coordination
Risk identification and mitigation
Experience with clinical systems (eTMF, CTMS, EDC, DCT)
Nice-to-have
Proactive and solutions-focused mindset
Strong interpersonal and collaboration skills
Ability to mentor junior team members
Resilient and adaptable in dynamic environments
Positive outlook and enthusiasm
Key Requirements
4-6 years clinical project management experience
Bachelor’s or advanced degree (Master’s, PharmD, PhD preferred)
Knowledge of FDA and regional regulations, ICH GCP Guidelines