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

📋 Description

• Establish and nurture robust relationships with key stakeholders at clinical trial sites, such as principal investigators, site coordinators, and research personnel.

• Offer support and direction to site staff regarding study protocols, procedures, and regulatory standards.

• Recognize opportunities to enhance site engagement and maximize site performance through ongoing communication and feedback channels.

• Collaborate with internal teams to create and execute site engagement strategies customized for each study and site.

• Track site performance metrics and deliver regular updates to study teams regarding site engagement initiatives and results.

• Participate in clinical research activities and take ownership of deliverables while working in a collaborative environment.

⛳️ Requirements

• A bachelor's degree in life sciences or a related discipline.

• Prior experience in clinical research, site management, or a similar field is preferred.

• Strong interpersonal and communication abilities, with a knack for building rapport and fostering effective working relationships with a diverse range of stakeholders.

• Exceptional organizational and problem-solving capabilities, with the ability to prioritize and manage multiple responsibilities concurrently.

• Familiarity with ICH-GCP guidelines and regulatory standards for clinical trials.

• Willingness to travel as necessary (approximately 60%).

• Legal eligibility to work in the country where the position is located.