Job Summary
The Clinical Research Associate (CRA) plays a pivotal role in the clinical trial process, overseeing and facilitating the progression of clinical studies. This position involves extensive interaction with clinical sites, ensuring that all trial protocols are adhered to diligently while maintaining compliance with regulatory standards. The CRA serves as a vital link between the sponsor and the clinical sites, ensuring data quality and study integrity.
Responsibilities
- Monitor clinical trials to ensure compliance with study protocols and regulatory requirements.
- Conduct site visits to evaluate site performance and address any issues that may arise.
- Review and verify study data for accuracy and completeness.
- Collaborate with site staff to provide training and resources necessary for successful trial execution.
- Assist in the preparation of study reports and documentation for regulatory submissions.
- Facilitate communication between the sponsor and the clinical sites, ensuring clarity of expectations.
Qualifications
- Bachelor’s degree in life sciences or a related field.
- Experience in clinical research, preferably as a CRA or in a related position.
- Strong understanding of GCP, FDA regulations, and clinical trial processes.
- Excellent communication and organizational skills.
- Ability to work independently and manage multiple projects simultaneously.
- Proficiency in data analysis and reporting tools.
Armata Pharmaceuticals, 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.
