Clinical Research Associate – Oncology & Hematology

About the role

Worldwide Clinical Trials is seeking a Clinical Research Associate (CRA) to support oncology and hematology studies across Czechia and Slovakia. You will work within a collaborative Clinical Operations team, contributing to the successful execution of clinical trials that aim to improve patient outcomes.

Key responsibilities

• Conduct site qualification, initiation, interim monitoring, and close‑out visits.
• Document findings from site visits in detailed written reports.
• Assess and train site staff on protocol adherence, safety information, and informed consent procedures.
• Perform source document verification to ensure data accuracy, patient safety, and regulatory compliance.
• Review case report forms (CRFs) using paper or electronic data capture (EDC) systems and assist sites with query resolution.
• Maintain Trial Master File (TMF) documentation, including updates related to investigational product (IP) receipt, accountability, and disposition.
• Provide mentorship to less‑experienced CRAs and support site staff as needed.

Required profile

• Strong interpersonal and communication skills, both oral and written.
• Ability to work independently while collaborating with cross‑functional teams.
• Attention to detail and commitment to high‑quality documentation.

Required skills

• Experience with source document verification.
• Familiarity with electronic data capture (EDC) systems.
• Knowledge of Trial Master File (TMF) management.
• Understanding of investigational product (IP) handling and accountability.