This is a fully remote position, open to applicants in Czechia.

📋 Description

• Accountable for site qualification, initiation, interim monitoring, site management, and conducting study close-out visits.

• Offer mentorship and support to junior CRAs and site personnel when necessary.

• Record site visit observations through written reports.

• Evaluate, oversee, and educate study site staff on adherence to protocols as required.

• Examine study subject safety information and informed consent documents.

• Carry out source document verification to ensure compliance, patient safety, and data accuracy.

• Review CRFs utilizing paper or electronic data capture systems and assist sites in resolving data queries.

• Provide necessary updates for site-related documentation to be filed in the Trial Master File (TMF).

⛳️ Requirements

• A minimum of 2 years of experience as a Clinical Research Associate.

• A 4-year university degree or an RN/BSN in Nursing.

• Experience in Oncology and Neurology is essential.

• Capacity to work independently with minimal supervision.

• Proficient in Microsoft Office, CTMS, and EDC Systems.

• Exceptional interpersonal, oral, and written communication skills in English.

🏝️ Benefits

• A diverse and inclusive workplace.

• Opportunities for mentorship and support.

• Assistance for career advancement.

• Promotion of collaborative efforts.