ICON plc is looking to hire an In-House Clinical Research Associate (IHCRA) to manage, implement, and monitor clinical studies in a team setting, ensuring compliance with ICON SOPs, SSPs, and all applicable rules and regulations.
Requirements
- Previous experience in clinical research or a related field preferred
Responsibilities
- Identifying, training/initiating and closing out of study sites.
- Managing study sites and the required protocols, amendments and/or deviations, assuring that data is reported accurately and timelines are maintained.
- Assists with timely preparation and submission of regulatory documents for IRB/IEC submissions according to local requirements, with support, as needed.
- Maintains Sponsor and patient confidentiality
- Actively participates in regular meetings with Project Managers
- Assists in development of site and patient enrolment strategies with project team; works to motivate sites to meet enrolment timelines.
- Developing knowledge of and compliance with local regulatory requirements.
Other
- Central and West region candidates only.
- Bachelor's degree in a relevant field, such as life sciences or healthcare
- Strong organizational and communication skills
- Ability to work independently and collaboratively in a fast-paced environment
- Attention to detail and ability to prioritize tasks effectively
