Job Summary
The Clinical Research Associate (CRA) plays a pivotal role in the management and monitoring of clinical trials. This position involves ensuring the integrity of data, compliance with regulatory requirements, and the overall successful conduct of clinical studies. The CRA collaborates closely with clinical teams to facilitate the execution of trials, ensuring that they adhere to the defined protocols and ethical standards.
Responsibilities
- Monitor clinical trials to ensure adherence to protocols and compliance with regulatory guidelines.
- Review and verify data collected during the trials for accuracy and completeness.
- Coordinate with clinical sites and personnel for the smooth operation of studies.
- Assist in the preparation of study documentation and reports.
- Conduct site visits to evaluate compliance and address any issues that arise during the trial.
- Facilitate communication among study stakeholders, including sponsors and investigators.
- Ensure timely submission of regulatory documents and reports.
Qualifications
- A degree in life sciences, nursing, or a related field.
- Previous experience in clinical research or a similar role is preferred.
- Familiarity with Good Clinical Practice (GCP) guidelines.
- Exceptional organizational and communication skills.
- Strong analytical skills with attention to detail.
- The ability to work independently and as part of a team in a fast-paced environment.
MiraVista Diagnostics 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.
