Global Clinical Project Lead – High-Impact

Crovelis

Madrid

On-site

EUR 60,000 - 90,000

Full time

12 days ago

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Job summary

Crovelis, the CRO division of Insud Pharma, is hiring a Clinical Project Manager to lead operational management of international clinical studies. You will drive studies forward while coordinating multidisciplinary teams, ensuring timelines, quality, budgets and regulatory compliance.

This is a dynamic, fast-growing environment with global project visibility and impact. The role requires 5–6+ years in clinical research, strong PM experience, and excellent English.

Qualifications

  • 5–6+ years of experience in Clinical Research.
  • Experience as Clinical Project Manager or in similar PM roles.
  • Strong knowledge of ICH-GCP and trial regulations.
  • International multicountry study experience.
  • Excellent communication and organizational skills.
  • Advanced English level.

Responsibilities

  • Lead and coordinate assigned clinical projects operationally.
  • Coordinate with Clinical Operations, Regulatory, Pharmacovigilance, Data Management, Biostatistics, QA and vendors.
  • Support study planning, risk management, timelines and budgets.
  • Ensure ICH-GCP compliance and SOPs/regulations.
  • Participate in study feasibility, site selection, oversight.
  • Contribute to stakeholder communications, study reporting and governance.
  • Support TMF oversight, audit readiness and close-out activities.
  • Work with CRAs, CTAs and international teams across regions.

Skills

Clinical research
Project management
ICH-GCP
International studies
Communication
English proficiency

Job description

Crovelis, the CRO division of Insud Pharma, is hiring a Clinical Project Manager to lead operational management of international clinical studies. You will drive studies forward while coordinating multidisciplinary teams, ensuring timelines, quality, budgets and regulatory compliance.

This is a dynamic, fast-growing environment with global project visibility and impact. The role requires 5–6+ years in clinical research, strong PM experience, and excellent English.

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