Job Summary
We are seeking a dedicated Clinical Research Associate (CRA) to join our team in Dallas, Texas. This role is pivotal in overseeing the conduct of clinical trials and ensuring compliance with regulatory standards. The CRA will collaborate closely with investigators and site staff to facilitate smooth operations throughout the study process.
Responsibilities
- Monitor clinical trial activities to guarantee adherence to protocols and regulations.
- Evaluate and confirm the qualifications and training of investigators.
- Provide support and guidance to site staff throughout the trial.
- Coordinate communication between the sponsor and the site, ensuring all information is processed efficiently.
Qualifications
- Experience in clinical research or in a related field is preferred.
- Strong understanding of regulatory requirements and good clinical practices.
- Excellent communication and interpersonal skills for effective collaboration with various stakeholders.
- Ability to manage multiple tasks and maintain attention to detail.
Medpace 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.
