Job Summary
The Clinical Research Associate (CRA) plays a vital role in conducting clinical trials and research studies for a full-service organization. The primary focus is to ensure the integrity of data collected during clinical investigations, adhering to regulatory requirements and standards. CRAs act as a liaison between the study sites, regulatory bodies, and the organization, ensuring seamless communication and effective project execution.
Responsibilities
- Oversee and manage clinical trial sites to guarantee compliance with study protocols and regulatory guidelines.
- Monitor the progress of clinical trials, ensuring timely data collection and reporting.
- Conduct site visits to evaluate trial progress and enhance participant engagement.
- Provide training and support to site staff on study protocols and procedures.
- Document and report any adverse events or discrepancies in accordance with organizational policies.
- Facilitate effective communication between stakeholders, including study sponsors and site personnel.
Qualifications
- Bachelor’s degree in life sciences, nursing, or a related field.
- Proven experience as a CRA or in a similar role within the clinical research environment.
- Strong understanding of Good Clinical Practice (GCP) and relevant regulatory requirements.
- Excellent organizational and problem-solving skills.
- Proficient in conducting data analysis and maintaining documentation.
- Effective communication and interpersonal skills to engage with diverse teams and stakeholders.
