ICON plc is a world-leading healthcare intelligence and clinical research organization. We’re proud to foster an inclusive environment driving innovation and excellence, and we welcome you to join us on our mission to shape the future of clinical development.
As a CRA I at ICON, you will contribute to our clinical trial operations function, working collaboratively to deliver high-quality outcomes across our clinical programmes.
What You Will Do
Your role will involve delivering clinical trial monitoring work to a high standard, working closely with your team and stakeholders.
Key Responsibilities Include
Working independently and actively to coordinate all activities for setting up and monitoring a study, completing accurate study status reports and maintaining study documentation
Running sponsor generated queries efficiently and taking responsibility for study cost efficiency; you will also participate in the preparation and review of study documentation and feasibility studies for new proposals as required.
Develop and maintain strong, collaborative relationships with key stakeholders, clinical investigators, and site staff.
Ensure patient safety by ensuring compliance with ICON's procedures, protocols, and regulatory requirements.
Your Profile
You will bring relevant clinical trial monitoring experience, along with the following qualifications and skills.
Required Qualifications And Experience
University degree in medicine, science, or equivalent
Knowledge of ICH-GCP guidelines and the expertise to review and evaluate medical data
Excellent written and verbal communication in English
Positive social skills enabling you to deal with queries in a timely manner
Willingness to travel as required (approximately 60%)
What ICON Can Offer You
Our success depends on the quality of our people. That’s why we’ve made it a priority to build a diverse culture that rewards high performance and nurtures
📌 Clinical Research Associate I (Bijaipur)
🏢 ICON Strategic Solutions
📍 Bijaipur
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