Job Summary
The Clinical Research Associate I will play a crucial role in executing clinical trials for medical devices. This entry-level position involves collaborating with research teams to ensure compliance with regulatory standards and the integrity of clinical data. The ideal candidate will contribute to the planning, monitoring, and completion of clinical studies while obtaining valuable experience in the field of clinical research.
Responsibilities
- Assist in the initiation, activation, and maintenance of clinical trial sites.
- Conduct regular site visits to monitor trial progress and ensure adherence to protocols.
- Review documentation to ensure compliance with regulations, protocols, and Good Clinical Practice (GCP).
- Support data collection and verification activities, ensuring accuracy and completeness of data.
- Provide training and guidance to site staff on study protocols and procedures.
- Communicate effectively with study teams, including investigators and site personnel, to resolve issues.
- Maintain study files and documentation in accordance with regulatory requirements and company policies.
Qualifications
- Bachelor’s degree in a relevant life science or healthcare field.
- Strong understanding of clinical research processes and regulatory requirements.
- Excellent organizational and communication skills.
- Ability to work independently and collaboratively in a team environment.
- Problem-solving skills and attention to detail.
- Willingness to travel to clinical sites as required.
