Senior Clinical Research Associate – Global Site Lead

Crovelis; Polska; On-site; PLN 262,000 - 393,000; Full time

Job summary

CROVELIS is seeking a Senior Clinical Research Associate to independently lead site management, start-up, monitoring, oversight and close-out of complex sites in Madrid. You will ensure data quality, patient safety and protocol compliance while delivering trials on time.

The role requires strong monitoring experience, high autonomy and a commitment to quality, with opportunities to work in an international environment and contribute to study execution.

Qualifications

• At least 5 years of experience in clinical research.
• Experience monitoring and independent site management.
• Experience in pharmaceutical, biotech, CRO/service provider or healthcare sectors.
• Strong knowledge of ICH-GCP and monitoring practices.
• Experience applying a risk-based oversight approach.

Responsibilities

• Independently manage assigned clinical trial sites through the study lifecycle.
• Conduct site initiation, routine monitoring and close-out visits per plan.
• Review source documents, CRFs and site records for accuracy and compliance.
• Ensure documentation is inspection-ready and up-to-date.
• Verify informed consent per protocol, ICH-GCP and regulations.
• Identify and manage site issues and operational risks.

Skills

Fluent English

Excellent communication

Organisational skills

Prioritisation

Problem-solving

Autonomy

Cross-functional collaboration

Coaching juniors

Microsoft Office

Clinical trial systems

Education

Bachelor's or Master's degree in Life Sciences, Pharmacy, Chemistry, Medicine, Nursing, Biotechnology

Tools

Microsoft Office

Clinical trial systems

Job description

CROVELIS is seeking a Senior Clinical Research Associate to independently lead site management, start-up, monitoring, oversight and close-out of complex sites in Madrid. You will ensure data quality, patient safety and protocol compliance while delivering trials on time.

The role requires strong monitoring experience, high autonomy and a commitment to quality, with opportunities to work in an international environment and contribute to study execution.