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

📋 Description

• Oversee clinical research operations at investigative sites engaged in Worldwide clinical studies.

• Evaluate and determine suitable research sites.

• Manage study initiation tasks, including regulatory documentation and the contract and budget procedures.

• Execute Pre-Site Selection Visits, Study Initiation Visits, Interim Monitoring Visits, and Closeout Visits.

• Educate site staff on protocol specifics, data gathering, and safety reporting obligations.

• Supervise site performance and deliver continuous support throughout the study's duration.

• Ensure informed consent is obtained, safety reporting is conducted, and regulatory standards are met.

• Collaborate with sites and study teams to enhance data integrity, ensure participant safety, and achieve study objectives.

• Assist in site closeout and the fulfillment of study requirements.

⛳️ Requirements

• A Bachelor's Degree or a Nursing Degree is required.

• A minimum of 5 years’ experience as a regional, traveling Clinical Research Associate.

• Proven track record in monitoring clinical trials.

• Willingness to travel within the designated region; approximately 6–8 days of travel per month.

• Experience in full-service monitoring is preferred.

• Strong understanding of clinical trial methodologies, site management, and regulatory guidelines.

• Candidates must be residents of Czechia.

• Ability to travel to research sites about 6–8 days each month.

🏝️ Benefits

• Equal employment opportunities provided without regard to race, color, ethnicity, ancestry, religion, national origin, gender, sex, gender identity or expression, sexual orientation, age, citizenship, marital or parental status, disability, military status, or any other class protected by applicable law.