Clinical Research Associate Salary: what to expect in this field.
Clinical research associates or CRAs have the responsibility of assisting the entire process of clinical
research. They also need to offer technical expertise at an advanced level in different steps like
collection of results, ordering tests, and handling supplies. It is also their responsibility to present very
specific information regarding the research to the general public.
Clinical research associates also handle different types of administrative tasks. They need to conform to
very strict safety and privacy regulations to avoid the occurrence of issues with different subjects and
any ethical concerns. CRAs need to be organized and they should be able to pay attention to all details
when they are conducting their research by applying different investigative methods in healthcare and
The expected salary
Many clinical research associates who are in the upper-levels like management can have a strong salary
upturn. The clinical trial managers can earn up to 97k dollars every year on average. Advancement in the
career of a clinical research associate leads them to become clinical project managers or even senior
clinical research associate. The median salaries for such positions are around 26k higher or 30k higher.
According to the survey, there is an indication that the clinical research associates have a large
professional skills toolkit. These include clinical research, oncology, and monitoring. These associates
tend to get more in terms of payment than the average. They may have a salary increase of up to 39
Clinical research associates have different duties which include the design, the planning, and the
implementation of the clinical research projects. They also oversee the overall clinical research
direction. They may also coordinate different activities of some colleagues in the company where they
work and in external entities.
A senior clinical research associate is looked upon to offer leadership in the activities involved in clinical
trials. They plan and implement the clinical trials that need to be carried out to ensure that all protocols
are adhered to.