Clinical Research Associate II – Contract Based

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

📋 Description

• Conduct and document all varieties of onsite monitoring visits.

• Engage in the initiation of studies.

• Execute CRF evaluations, source document verification, and resolution of queries.

• Oversee communication and relationships with sites.

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

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

• Participate in quality assurance processes, including compliance monitoring and report evaluations.

• Contribute to feasibility assessments.

• Assist the regulatory team in preparing documentation for study submissions.

• Establish and nurture relationships with clinical sites and investigators.

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

⛳️ Requirements

• Bachelor's degree in Life Sciences or an equivalent combination of education, training, and experience.

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

• Experience in all forms of monitoring visits during Phase II and/or III.

• Mandatory experience in IBD/Inflammatory Bowel Diseases.

• Fluent proficiency in both English and Portuguese.

• Competence in MS Office applications.

• Ability to plan, multitask, and operate effectively in a dynamic team setting.

• Strong communication, collaboration, and problem-solving abilities.

• Willingness to travel.

🏝️ Benefits

• Flexible remote/home-based (freelance) work arrangement.

• Opportunities for professional development and career advancement.

• Chance to collaborate with a stable and innovative Contract Research Organization.