Clinical Research Associate: Monitoring & Trial Quality

Pharmaxi LLC.

Warszawa

On-site

PLN 120,000 - 180,000

Full time

14 days+

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Benefits offered by this job

Career development opportunities
International projects exposure
Supportive clinical research team

Job summary

Pharmaxi LLC. is seeking a Clinical Research Associate to support the delivery of clinical trials through site monitoring, documentation control and collaboration with project teams. You will ensure GCP compliance and data quality while working with international sites.

The role requires independent work, attention to detail, and strong communication skills. On-site Warsaw position offering opportunities to develop in monitoring and trial quality management.

Qualifications

  • Experience in clinical trial monitoring or in clinical research.
  • Knowledge of GCP principles and regulatory requirements for clinical trials.
  • Good organizational skills and ability to manage documentation.
  • Communication skills and ability to cooperate with investigational sites.
  • Knowledge of English sufficient to work with project documentation.

Responsibilities

  • Monitor clinical trials in accordance with the protocol and GCP requirements.
  • Cooperate with investigational sites, investigators and site personnel.
  • Verify clinical trial documentation and data completeness.
  • Prepare monitoring visit reports.
  • Identify risks, deviations and operational issues.
  • Collaborate with Project Manager, CTA, regulatory affairs and data management.
  • Support site preparation for study start-up, conduct and close-out.

Skills

Site Monitoring
GCP Knowledge
Documentation
Communication
English Proficiency

Tools

EDC
eTMF

Job description

Pharmaxi LLC. is seeking a Clinical Research Associate to support the delivery of clinical trials through site monitoring, documentation control and collaboration with project teams. You will ensure GCP compliance and data quality while working with international sites.

The role requires independent work, attention to detail, and strong communication skills. On-site Warsaw position offering opportunities to develop in monitoring and trial quality management.

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