Clinical Research Associate I

Role Summary

As a Clinical Research Associate I at ICON, you will play a vital role in clinical trial operations, working collaboratively to ensure outstanding results throughout the clinical programs.

Primary Duties

• Independently managing and coordinating all tasks involved in study setup and ongoing monitoring, including preparing precise study status reports and maintaining thorough documentation.
• Efficiently resolving queries generated by sponsors, managing study cost-effectiveness, and assisting in preparing and reviewing documentation and feasibility assessments for new study proposals as necessary.
• Building and nurturing strong, cooperative relationships with stakeholders, clinical investigators, and site personnel.
• Ensuring patient safety by adhering strictly to ICON's protocols, procedures, and all applicable regulatory guidelines.

Candidate Profile

• Holds a university degree in medicine, science, or a related field.
• Thorough understanding of ICH-GCP guidelines with competence in reviewing and assessing medical data.
• Proficient communication skills in English, both written and spoken.
• Interpersonal skills that facilitate prompt and effective query management.
• Prepared to travel as needed, typically between 60% to 75% of the time.