Clinical Research Professional
hace 2 semanas
Job Summary
We are seeking a Clinical Associate to support the design, implementation, and management of clinical trials. This role will involve assisting in the planning, execution, and monitoring of clinical trials, ensuring adherence to protocol requirements, regulatory guidelines, and industry standards.
Key Responsibilities
- Assist in the planning, execution, and monitoring of clinical trials
- Coordinate study activities including site initiation, patient recruitment, data collection, and monitoring visits
- Collaborate with cross-functional teams to support the successful execution of clinical trials
- Maintain comprehensive study documentation and records
- Support study close-out activities including data cleaning, analysis, and preparation of clinical study reports
Requirements
To be successful in this role, you will need a Bachelor's or advanced degree in Life Sciences, Health Sciences, or a related field, and previous experience in clinical research or healthcare. You should also have strong organizational and time management skills, with the ability to prioritize tasks and manage competing priorities effectively.
About Us
ICON plc is a world-leading healthcare intelligence and clinical research organization. We are 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.
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