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

📋 Description

• Execute clinical trial monitoring tasks to a high standard.

• Oversee all processes involved in setting up and monitoring a study.

• Produce precise study status reports and manage study documentation.

• Address sponsor-generated queries promptly and take ownership of study cost efficiency.

• Engage in the preparation and evaluation of study documentation and feasibility studies for new proposals as necessary.

• Foster and sustain collaborative relationships with key stakeholders, clinical investigators, and site personnel.

• Ensure patient safety and adherence to ICON's protocols, procedures, and regulatory standards.

⛳️ Requirements

• Bachelor's degree in medicine, science, or a related field.

• Minimum of 1 year of experience as a Clinical Research Associate (CRA) with on-site monitoring.

• Familiarity with ICH-GCP guidelines.

• Ability to review and assess medical data effectively.

• Strong written and verbal communication skills in English.

• Effective interpersonal skills for timely resolution of queries.

• Willingness to travel as needed (approximately 60%).

• Legal authorization to work in the country where the position is located.

🏝️ Benefits

• Competitive base salary along with performance-based incentives.

• Health and wellness programs, including medical, dental, and vision coverage where applicable.

• Retirement and pension plans available.

• Life insurance and disability coverage provided.

• Employee assistance programs and wellness resources offered.

• Opportunities for learning and development through structured training and career pathways.