Job Summary
The In-House Clinical Research Associate plays a vital role in overseeing clinical trial operations and ensuring compliance with regulatory requirements. This position serves as a link between the clinical team and other departments, facilitating smooth project management and the execution of clinical studies.
Responsibilities
- Manage the planning, execution, and reporting of clinical trials.
- Coordinate with cross-functional teams to ensure adherence to protocols and timelines.
- Perform data collection, entry, and accuracy checks throughout the study lifecycle.
- Facilitate training sessions for study personnel on clinical trial procedures and compliance standards.
- Monitor study progress and prepare detailed reports on findings and outcomes.
- Maintain regular communication with regulatory bodies to ensure all trial activities meet legal standards.
Qualifications
- Bachelor’s degree in life sciences, nursing, or a related field; advanced degrees are a plus.
- Proven experience in clinical research or clinical operations.
- Strong understanding of Good Clinical Practice (GCP) guidelines and regulatory requirements.
- Excellent organizational, analytical, and communication skills.
- Ability to work independently and as part of a team in a fast-paced environment.
Alira Health 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.
