WHAT IS AN on-site clinical research associate (traveling/remote) jobs?
An on-site Clinical Research Associate (CRA) is a professional who is responsible for monitoring clinical trials conducted by pharmaceutical companies, biotech firms, and medical device manufacturers. On-site CRAs are typically employed by Contract Research Organizations (CROs) that provide outsourced clinical research services to their clients. This position requires the CRA to travel to various clinical trial sites to oversee the trials and ensure compliance with regulations and protocols. However, some CRAs may also work remotely from their home office, depending on the requirements of the project.
WHAT USUALLY DO IN THIS POSITION?
The primary role of an on-site CRA is to ensure that clinical trials are conducted in compliance with the protocols, Standard Operating Procedures (SOPs), Good Clinical Practices (GCPs), and relevant regulatory guidelines. They are responsible for monitoring the conduct of clinical trials, including data collection, drug accountability, adverse event reporting, and ensuring the safety and well-being of trial subjects. Additionally, they are responsible for maintaining communication with study site personnel, study sponsors, and regulatory authorities.
TOP 5 SKILLS FOR POSITION
- Attention to Detail
- Communication Skills
- Analytical Thinking
- Organizational Skills
- Project Management Skills
HOW TO BECOME THIS TYPE OF SPECIALIST?
To become an on-site CRA, a Bachelor's degree in life sciences, nursing, or a related field is typically required. Additionally, some employers may require a Master's degree or an equivalent certification in clinical research. Some CRAs may gain entry-level experience through internships or entry-level positions in clinical research. However, most employers prefer candidates with at least 1-2 years of experience in clinical research.
AVERAGE SALARY
According to Glassdoor, the average salary for an on-site CRA in the United States is approximately $79,000 per year. However, salaries may vary depending on factors such as years of experience, location, and employer.
ROLES AND TYPES
There are various roles and types of CRAs, including on-site CRAs, remote CRAs, and in-house CRAs. On-site CRAs are responsible for traveling to clinical trial sites to monitor the trials, while remote CRAs work from their home office and monitor the trials through electronic data capture systems. In-house CRAs work from the sponsor's office and are responsible for overseeing the trial conduct and data management. In addition to these roles, there are also Lead CRAs, who are responsible for managing a team of CRAs, and Senior CRAs, who have more experience and are responsible for complex trials.
LOCATIONS WITH THE MOST POPULAR JOBS IN USA
The locations with the most popular on-site CRA jobs in the United States include California, Texas, New York, Massachusetts, and Pennsylvania. These states have a high concentration of pharmaceutical, biotech, and medical device companies, which create opportunities for clinical research professionals.
WHAT ARE THE TYPICAL TOOLS?
On-site CRAs typically use a range of tools and technologies to monitor clinical trials, such as Electronic Data Capture (EDC) systems, Clinical Trial Management Systems (CTMS), and Interactive Voice Response Systems (IVRS). They also use various communication tools such as email, phone, and video conferencing to maintain communication with study site personnel, study sponsors, and regulatory authorities.
IN CONCLUSION
On-site Clinical Research Associate (CRA) jobs involve traveling to various clinical trial sites or working remotely from home to monitor the conduct of clinical trials. This position requires a Bachelor's degree in life sciences, nursing, or a related field, with at least 1-2 years of experience in clinical research. The primary responsibilities of an on-site CRA include ensuring compliance with protocols, SOPs, GCPs, and relevant regulatory guidelines, monitoring the conduct of clinical trials, and maintaining communication with study site personnel, study sponsors, and regulatory authorities. The average salary for this position is approximately $79,000 per year. CRAs use a range of tools and technologies such as EDC systems, CTMS, and IVRS to monitor clinical trials and maintain communication. The most popular locations for on-site CRA jobs in the United States are California, Texas, New York, Massachusetts, and Pennsylvania.