Senior Clinical Research Associate - Remote & On-Site

Parexel; Polska; Hybrid; PLN 230,000 - 260,000; Full time

Benefits offered by this job

Premium salary

Car or car allowance

Medical care plan: Health, Dental &amp

Life Assurance

Excellent training

Job summary

Parexel is hiring a Clinical Research Associate (CRA) for Northern Poland (Trojmiasto, Poznan, Koszalin) as an individual contributor. You will manage allocated sites, perform remote and on-site monitoring, and ensure rights, safety, and well-being of subjects across all trial phases.

You will collaborate with sponsors, investigators, and site staff, maintaining inspection-ready documentation, and contributing to process improvement within a growth-oriented environment.

Qualifications

• Minimum 2 years of direct site monitoring experience in bio/pharma/CRO.
• Fluent in local language and in English, both verbal and written.
• Ability to travel domestically and internationally for ~65–75% of time.

Responsibilities

• Serve as the primary site contact and site manager across all phases of a clinical study.
• Monitor study data to ensure completeness, accuracy, and unbiased results in line with ICH-GCP and SOPs.
• Coordinate with sponsors, investigators and site staff on protocol conduct and regulatory documentation.
• Record visit reports promptly and maintain essential trial documentation in systems.
• Support audits and inspections and contribute to CRA knowledge sharing.

Skills

Site management

Monitoring

Data analysis

Time management

Communication

Education

Bachelor's degree in science (Biotechnology, Pharma, Biology)

Tools

MS Office

eTMF/Clinical IT systems

Job description

Parexel is hiring a Clinical Research Associate (CRA) for Northern Poland (Trojmiasto, Poznan, Koszalin) as an individual contributor. You will manage allocated sites, perform remote and on-site monitoring, and ensure rights, safety, and well-being of subjects across all trial phases.

You will collaborate with sponsors, investigators, and site staff, maintaining inspection-ready documentation, and contributing to process improvement within a growth-oriented environment.