What is a clinical trial associate job?
A clinical trial associate (CTA) is a professional who assists in the management and coordination of clinical trials. These professionals are responsible for ensuring the trials run smoothly, comply with regulations, and are completed on time. CTAs may work for pharmaceutical companies, research organizations, or contract research organizations (CROs).
What do clinical trial associates usually do in this position?
Clinical trial associates are responsible for a variety of tasks, including:
- Assisting with the planning and implementation of clinical trials
- Ensuring compliance with FDA regulations and guidelines
- Managing and organizing trial data
- Coordinating with study sites and investigators
- Preparing study documentation and reports
Top 5 skills for this position:
- Attention to detail
- Organizational skills
- Strong communication skills
- Ability to work independently
- Knowledge of FDA regulations and guidelines
How to become a clinical trial associate?
To become a clinical trial associate, you typically need a bachelor's degree in a related field, such as life sciences or healthcare. Relevant work experience is also important, as well as knowledge of FDA regulations and guidelines. Some employers may also require certification as a clinical research associate (CRA) or clinical research professional (CCRP).
Average salary:
According to Glassdoor, the average salary for a clinical trial associate in the United States is around $65,000 per year. However, salaries can vary depending on experience, location, and employer.
Roles and types:
Clinical trial associates can work in a variety of roles, including:
- Clinical research associate (CRA)
- Clinical project coordinator
- Clinical trial assistant
- Clinical data coordinator
Locations with the most popular jobs in USA:
Some of the top locations for clinical trial associate jobs in the United States include:
- Boston, MA
- San Francisco, CA
- New York, NY
- Chicago, IL
- San Diego, CA
What are the typical tools used in this position?
Clinical trial associates may use a variety of tools and software to manage and organize trial data, including:
- Electronic data capture (EDC) systems
- Clinical trial management systems (CTMS)
- Regulatory document management systems (RDMS)
- Microsoft Excel or other spreadsheet software
- Project management software
In conclusion:
Clinical trial associates play a vital role in the management and coordination of clinical trials. They are responsible for ensuring that trials run smoothly, comply with regulations, and are completed on time. To become a clinical trial associate, you typically need a bachelor's degree in a related field, relevant work experience, and knowledge of FDA regulations and guidelines. Salaries for clinical trial associates can vary depending on experience, location, and employer.