Associate Specialist, Clinical Research

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

📋 Description

• Ensures the execution of clinical trials adhering to established standards.

• Serves as the main point of contact and manager during all phases of clinical research.

• Cultivates robust relationships with site personnel.

• Conducts site management and monitoring tasks.

• Engages in site selection and qualification processes.

• Performs site visits and generates timely reports.

• Maintains communication with investigators and site staff members.

• Oversees documentation within CTMS, eTMF, and other relevant systems.

⛳️ Requirements

• Proficient in both Portuguese and English, both spoken and written.

• Outstanding communication abilities.

• Strong comprehension and hands-on experience in clinical research and the various phases of clinical trials.

• Current knowledge of GCP/ICH guidelines as well as local laws and regulations pertaining to clinical research.

• Proficiency in IT skills, including MS Office and clinical IT applications.

• Aptitude for understanding and interpreting data and metrics.

• Ability to navigate and manage complex issues effectively.

🏝️ Benefits

• Flexible work arrangements: Remote.

• Dedication to prioritizing the patient in all our endeavors.

• A diverse and inclusive workplace culture.