Clinical Research Associate – Oncology, Hematology

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

📋 Description

• Oversee site qualification, initiation, interim monitoring, site management, and closing visits for studies.

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

• Record findings from site visits through comprehensive written reports.

• Evaluate, monitor, and educate study site personnel on adherence to protocols as needed.

• Assess study subject safety information and obtain informed consent documentation.

• Perform source document verification to ensure compliance, patient safety, and accuracy of data.

• Review Case Report Forms (CRFs) utilizing both paper and electronic data capture systems, assisting sites with data query resolutions.

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

• Ensure compliance at sites regarding the receipt, accountability, and proper return or destruction of investigational products (IP).

• Conduct site visits alongside other CRAs for evaluation or training purposes as requested and appropriate.

⛳️ Requirements

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

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

• Required experience in Oncology and Hematology.

• Proficient in Microsoft Office, Clinical Trial Management Systems (CTMS), and Electronic Data Capture (EDC) Systems.

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

• Strong organizational abilities with a keen attention to detail.

• Capability to work independently with minimal supervision.

🏝️ Benefits

• Health insurance.

• Opportunities for professional development.

• Flexible working arrangements.