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.
Syneos Health Inc provides equal employment opportunities to all employees and applicants for employment and prohibits discrimination and harassment of any type without regard to race, color, religion, age, sex, national origin, disability status, genetics, protected veteran status, sexual orientation, gender identity or expression, or any other characteristic protected by federal, state or local laws.
