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

📋 Description

• Accountable for site qualification, initiation, interim monitoring, site management, and concluding study visits.

• Record site visit observations through comprehensive written reports.

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

• Assess study subject safety information and informed consent documentation.

⛳️ Requirements

• Minimum of 2 years of experience as a Clinical Research Associate.

• Bachelor’s degree from a 4-year university or an RN/BSN in Nursing.

• Required experience in Hematology, Oncology, and Cardiometabolic (Obesity, T1D/T2D, GLP).

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

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

🏝️ Benefits

• Mentoring and guidance are provided.

• A collaborative and supportive work environment.

• Opportunity to engage with diverse therapeutic areas.