Clinical Research Associate II – Contract

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

📋 Description

• Execute and document various types of onsite monitoring visits

• Engage in study initiation processes

• Conduct CRF assessments, verify source documents, and resolve queries

• Oversee communication with study sites

• Manage study operations, timelines, and schedules at the national level

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

• Involve in quality assurance, including compliance monitoring and report evaluation

• Contribute to feasibility assessments

• Assist the regulatory team in preparing materials for study submissions

• Foster and nurture relationships with clinical sites and investigators

• Ensure adherence to timelines, objectives, and standards of clinical research projects

• Prioritize the rights, safety, well-being of subjects, and compliance with data quality standards

⛳️ Requirements

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

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

• Background in all types of monitoring visits during Phase II and/or III

• Essential experience in IBD/Inflammatory Bowel Diseases

• Proficient in both English and Portuguese

• Competency in MS Office applications

• Capability to plan, manage multiple tasks, and work within a dynamic team environment

• Strong communication, collaboration, and problem-solving skills

• Willingness to travel

🏝️ Benefits

• Investment in professional development and career advancement

• Flexible remote/home-based work arrangement

• Engagement on a freelance contract basis