Job Summary
The Home-Based Experienced Clinical Research Associate (CRA) plays a vital role in the successful execution of clinical trials. This position involves working remotely while maintaining a strong focus on project management within clinical settings, ensuring that studies are conducted according to regulatory guidelines and standards. The CRA will be a key liaison between sponsors, site staff, and other stakeholders, contributing to the oversight of clinical trial sites.
Responsibilities
- Manage and monitor clinical trials from initiation through to completion.
- Conduct site assessments, initiation visits, and monitoring visits.
- Ensure compliance with Good Clinical Practice (GCP) and regulatory requirements.
- Review and verify clinical data for accuracy and completeness.
- Coordinate site communication and act as a point of contact for query resolution.
- Prepare and submit reports on trial progress and any issues encountered.
Qualifications
- Bachelor’s degree in life sciences, nursing, or related field.
- Proven experience in clinical monitoring or as a CRA in a similar environment.
- Strong knowledge of GCP, ICH, and regulatory guidelines.
- Excellent organizational and communication skills.
- Ability to work independently and manage multiple projects effectively.
- Proficiency in using electronic data capture and clinical trial management systems.
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.
