Job Summary
The Remote In-House Clinical Research Associate will play a pivotal role in supporting clinical trials and ensuring compliance with regulatory standards. This position involves collaborating with cross-functional teams to facilitate the successful execution of clinical studies while maintaining high-quality research practices. The ideal candidate will be proactive, detail-oriented, and possess strong communication skills to effectively manage responsibilities in a remote setting.
Responsibilities
- Coordinate and oversee clinical trial operations to ensure adherence to protocols and regulatory guidelines.
- Maintain accurate and up-to-date study documentation and reports.
- Assist in the selection and management of investigative sites.
- Monitor study progress through regular communication with clinical sites.
- Provide training and support to site personnel regarding study procedures and compliance.
- Participate in data collection, cleaning, and analysis as needed.
- Prepare for and assist with audits and inspections from regulatory authorities.
Qualifications
- Bachelor’s degree in a related field, such as life sciences or healthcare.
- Experience in clinical research, preferably in a similar role.
- Strong understanding of Good Clinical Practice (GCP) and regulatory requirements.
- Proficient in data management and electronic data capture systems.
- Excellent organizational skills and attention to detail.
- Effective communication and interpersonal abilities.
- Ability to work independently in a remote 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.
