Job Summary
A growing mid-sized, global Contract Research Organisation (CRO) is seeking a Clinical Research Associate II/III to join its team onsite in the United States. This role is central to the delivery of agile and patient-centered clinical development solutions, contributing to advancements in scientific research.
Responsibilities
- Collaborate with potential investigators and institutions to discuss and establish study budgets.
- Support the conduct of clinical trials through effective management and oversight of study processes.
- Ensure compliance with regulatory requirements and company standards during research activities.
- Assist in the documentation and monitoring of clinical trial progress and results.
- Engage in the preparation and review of study protocols and other essential documents.
Qualifications
- Experience in clinical research as a Clinical Research Associate, preferably at the II/III level.
- Relevant educational background in sciences, nursing education, or a healthcare-related field.
- Proven ability to effectively collaborate with multiple stakeholders in the clinical trial process.
- Strong knowledge of regulatory requirements and best practices in clinical research.
- Excellent organizational and communication skills to manage study logistics and documentation.
