Clinical Research Associate II – Contract Based

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

📋 Description

• Engage directly with project stakeholders to facilitate effective communication.

• Ensure adherence to timelines, goals, and standards in clinical research projects.

• Develop and sustain relationships with clinical sites and investigators.

• Prioritize the rights, safety, and well-being of subjects while ensuring data quality compliance.

• Execute and document all types of onsite monitoring visits.

• Contribute to the startup phase of studies.

• Conduct CRF reviews, verify source documents, and resolve queries.

• Oversee site communication and management.

• Monitor study activities, timelines, and schedules at the national level.

• Act as a liaison for in-house support services and vendors.

• Engage in quality control measures, including compliance monitoring and review of reports.

• Take part in feasibility studies.

• Assist the regulatory team in the preparation of documents for study submissions.

⛳️ Requirements

• Bachelor’s degree in Life Sciences or a comparable combination of education, training, and experience.

• At least 1 year of independent on-site monitoring experience in Portugal.

• Familiarity with all types of monitoring visits in Phase II and/or III studies.

• Proficient in both English and Portuguese.

• Competent in MS Office applications.

• Strong planning, multitasking abilities, and capability to work in a fast-paced team environment.

• Excellent communication, collaboration, and problem-solving skills.

• Willingness to travel as required.

🏝️ Benefits

• Opportunities for professional development and a commitment to career growth.

• Flexible home-based (freelance) work arrangement.