The Clinical Trials Assistant Role
a Perfect role for Newcomers in Clinical Research
If you’re interested in the healthcare industry, but don’t know where to start, consider becoming a Clinical Trials Assistant (CTA). This role can provide a valuable entry point into the world of clinical research, with opportunities for growth and career advancement. In this blog post, we’ll explore the benefits of a CTA role and why it’s a great choice for newcomers in clinical research.
Why Choose a CTA Role as a Newcomer?
The salary for a CTA can vary based on factors such as location, experience, and employer. In the United States, the median annual salary for a clinical trials assistant is around $49,000, with a range typically falling between $38,000 to $62,000. However, salaries can be higher or lower depending on the specific job and its location. It’s always a good idea to research the specific job and employer you are interested in to get a better understanding of the salary range.
The CTA ROLE
A Clinical Trials Assistant (CTA) is a member of the clinical research team responsible for supporting the planning and execution of clinical trials. CTAs typically work in a fast-paced and dynamic environment, assisting with trial coordination, data entry and management, regulatory compliance, and communication and collaboration with other team members.
Typical CTA tasks and responsibilities
The job responsibilities of a CTA can vary depending on the employer and the specific role. Some common job responsibilities of a CTA are:
Assisting with trial coordination: CTAs may help with the coordination of trial-related activities, such as scheduling participant visits, preparing study materials, and managing study supplies.
Data entry and management: CTAs may be responsible for entering data into study databases, tracking study progress, and monitoring participant safety and data quality.
Regulatory compliance: CTAs may help ensure that trials are conducted in compliance with regulatory requirements and study protocols, which may include preparing regulatory submissions, maintaining study documentation, and assisting with audits or inspections.
Communication and collaboration: CTAs may work closely with other members of the clinical research team, such as study coordinators, investigators, and sponsors, and may also communicate with study participants and their families.
Overall, the job responsibilities of a CTA involve supporting the clinical research team and contributing to the successful completion of clinical trials, with a focus on accuracy, efficiency, and adherence to study protocols and regulations.
Multiple Educational Backgrounds work
While a degree in life sciences or healthcare can be helpful, it’s not always a requirement for this specific role in clinical research. Strong organizational skills, attention to detail, and the ability to work well in a team are essential qualities for success in these roles. Any degree program that has provided you with these skills can be a good fit, including business, psychology, or even engineering.
To become a Clinical Trials Assistant (CTA), you typically need at least a high school diploma or equivalent. However, some employers may prefer some post-secondary education, such as an associate’s or bachelor’s degree in a related field, such as life sciences or healthcare.
While formal education can be helpful, relevant work experience can also be valuable for a clinical trials assistant role. Experience in a healthcare setting, such as working in a hospital or clinical research center, can demonstrate relevant skills and familiarity with the industry.
Other key skills and traits that can be beneficial for a clinical trials assistant include attention to detail, strong organizational and communication skills, the ability to follow protocols and regulations, and a willingness to learn and adapt in a fast-paced environment.
Ultimately, the specific qualifications and requirements for a clinical trials assistant role can vary depending on the employer and the job responsibilities.
Become Trained and Certified as a CTA
If you’re interested in becoming a Clinical Trials Assistant (CTA), consider obtaining your certification through VIARES. We offers a comprehensive training and certification program for clinical research professionals, including the CTA certification.
With VIARES, you’ll receive high-quality training from experienced professionals in the field, gain practical skills and knowledge, and be prepared to take your career in clinical research to the next level. Don’t wait – start your journey towards becoming a certified CTA with VIARES today.
The Clinical Trials Assistant role is an excellent entry point for newcomers to the healthcare and research industries. With opportunities for growth and career advancement, a CTA role can be a rewarding and fulfilling career choice. Become certified as a CTA by VIARES and take the first step towards a career in clinical research.
Hear from our Graduates
VIARES already supported 5500+ talents from 100+ countries on all continents. Here is a Snapshot of Graduate Experience and how they benefited from our Clinical Research Training Courses and Job Support.
IzabelaClinical Trial Administrator, IQVIA
I wanted to progress in my career, as I already was working in the field of clinical research. For me the course was a great experience, I learned a lot. I was able to broaden my knowledge about clinical trials and now
I feel prepared for the interviews and career steps to come! The teachers were extremely good trained and it was a pleasure to learn from them.
VassilClinical Coordinator, KCR CRO
Proud to announce that I have passed the Final Exam on the VIARES Clinical Research Talent Program. I strongly recommend it to all people interested in the field of clinical trials. Of course many thanks to Dietmar Eglhofer for creating this program
and all the great tutors: Eric Klaver, Gavin Chait and Gabriele Disselhoff.
ShilpaMSL Team Manager, Abbott
The VIARES Clinical Research Talent Program provided me a great opportunity to refresh and rebuild my clinical research skills and competencies. The program was well structured and covered the key aspects related to clinical research, drug
development, ICH guidelines, and clinical research regulations. The self-learning modules, followed by live webinars led by subject matter experts, provided the participants a platform to understand the key concepts and engage in great dialogue and discussions. I thank VIARES for giving me this opportunity and highly recommend this program to professionals looking to start a career in clinical research.
IwonaClinical Trial Administrator, DOCS (ICON) with Janssen
VIARES Academy supported me at every step in my course and answered my questions instantly. Moreover the platform is very organized and I could find my way around very fast.
The course content provided by the courses at VIARES have helped me to improve my knowledge at my current job as a clinical trials assistant.