Clinical Project Manager

Crovelis; Madrid; On-site; EUR 60,000 - 90,000; Full time

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

We are hiring | Clinical Project Manager – Crovelis

At Crovelis, the CRO division of Insud Pharma, we are continuing to grow and are looking for a Clinical Project Manager to join our team and lead the operational management of international clinical studies.

We are looking for someone with solid experience in clinical research and project management, capable of driving studies forward while coordinating multidisciplinary teams and ensuring timelines, quality standards, budgets, and regulatory compliance are successfully met.

This is an opportunity to join a dynamic, collaborative, and fast-growing environment where you will have real visibility and impact across global clinical projects.

What will you do?

• Lead and coordinate assigned clinical projects from an operational perspective
• Collaborate cross-functionally with Clinical Operations, Regulatory, Pharmacovigilance, Data Management, Biostatistics, QA and external vendors
• Support study planning, risk management, timelines and budget tracking
• Ensure compliance with ICH-GCP, SOPs and applicable regulations
• Participate in study feasibility, site selection and project oversight activities
• Contribute to stakeholder communication, study reporting and project governance
• Support TMF oversight, audit readiness and study close-out activities
• Work closely with CRAs, CTAs and international teams across multiple regions

What are we looking for?

• 5–6+ years of experience in Clinical Research
• Previous experience as Clinical Project Manager or in similar project management roles
• Strong understanding of ICH-GCP and clinical trial regulations
• International and multicountry study experience highly valued
• Excellent communication, coordination and organizational skills
• Proactive, solution-oriented and able to work in fast-paced environments
• Advanced English level

What do we offer?

• Stable opportunity within an international pharmaceutical group
• Exposure to global and high-impact clinical projects
• Collaborative and multidisciplinary environment
• Professional growth and development opportunities

If you are looking for your next challenge in Clinical Research and want to be part of a company with an entrepreneurial mindset and international reach, we would love to hear from you.