Job Summary
The Clinical Research Associate I (CRA I) plays a crucial role in overseeing clinical trials and ensuring compliance with regulatory standards. This position involves monitoring various aspects of clinical studies, ensuring data integrity and subject safety while collaborating with research teams to facilitate the smooth progression of trials.
Responsibilities
- Conduct site visits to assess and monitor clinical trial sites, ensuring adherence to study protocols and regulatory requirements.
- Document and report findings from site visits, addressing any issues or concerns promptly.
- Support the initiation and closure of clinical sites, ensuring that all necessary documentation is in place.
- Assist in the training of site staff on protocol requirements and study procedures.
- Maintain accurate and timely study records and reports.
- Collaborate with cross-functional teams, including project managers and data managers, to ensure optimal trial execution.
Qualifications
- A bachelor’s degree in life sciences or a related field is preferred.
- Experience in clinical research or a related field is advantageous but not mandatory.
- Strong attention to detail and organizational skills.
- Excellent communication and interpersonal abilities.
- Ability to work collaboratively in a team environment and manage multiple tasks efficiently.
- Familiarity with Good Clinical Practice (GCP) guidelines is a plus.
