Clinical Research Associate II

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

📋 Description

• Execute and document various onsite monitoring visits.

• Participate in the initiation of studies.

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

• Manage site communications and responsibilities.

• Serve as a liaison for internal support services and vendors.

• Liaise with internal project teams concerning the progress of the study.

• Engage in the site identification process.

• Assist the regulatory team in compiling documents for study submissions.

• Prepare for and engage in audits and inspections.

⛳️ Requirements

• Bachelor’s degree in Life Sciences or a related field.

• Minimum of 2 years of independent onsite monitoring experience in Portugal.

• Experience in Oncology or Hematology is advantageous.

• Proficient in Portuguese, English, and MS Office applications.

• Capable of planning, multitasking, and thriving in a dynamic team setting.

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

• Willingness to travel and possess a valid driver’s license.

🏝️ Benefits

• Comprehensive training programs.

• In-depth therapeutic area training.

• Monitors training program.

• Mentorship opportunities.

• Engaging soft skills training sessions.