Remote Clinical Research Associate Position
2 weeks ago
At the forefront of clinical research and development, we are seeking an experienced Clinical Research Associate to join our dynamic team. This role involves overseeing and coordinating clinical trials from setup to completion, ensuring meticulous compliance with regulatory requirements.
The successful candidate will be responsible for:
- Coordination of all activities related to study setup and monitoring, along with maintaining accurate study documentation and reporting
- Efficient management of sponsor-generated queries and optimization of study cost efficiency, with participation in the preparation and review of study documents and feasibility studies as required
- Development of strong relationships with key stakeholders, clinical investigators, and site staff through effective communication and collaboration
- Ensuring patient safety by adhering to ICON's procedures, protocols, and regulatory standards
This is a home-based position that requires a significant amount of travel (at least 60% of the time) and possession of a valid driver's license.
Key Requirements:
- University degree in medicine, science, or equivalent qualification
- Proven knowledge of ICH-GCP guidelines and expertise in reviewing and evaluating medical data
- Excellent written and verbal communication skills in English
- Strong social skills enabling timely resolution of queries
- Valid driver's license and ability to travel extensively internationally and domestically
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