Clinical Research Associate Certification 2025

clinical research associate

A career as a Clinical Research Associate 2025 (CRA) offers a challenging and rewarding path to work on new medications that will improve the lives of patients. CRAs are involved in clinical trials that test the effectiveness and safety of drugs, medical devices, and other treatments.

CRAs are required to meet many qualifications, including a bachelor’s degree in life science or healthcare. These qualifications include a training program that teaches them how to identify problems in a trial.

Free Clinical Research Associate Practice Test Online

Clinical Research Associate

Every pill, vaccine, therapy and medical device that you might take or use to improve your health undergoes clinical research before it gets approval. You can be part of this process, working as a clinical research associate (CRA). This career is ranked fourth on CNN Money’s Best Jobs in America list. CRAs act as liaisons between those who sponsor the trials and the people who facilitate them. This job is incredibly rewarding and provides the chance to work on trials that have the potential to save lives.

You can find a position as a CRA in hospitals, universities, government agencies and pharmaceutical companies. Inexperienced graduates may be able to enter the industry as a clinical trials administrator or assistant, with the aim of progressing to a CRA role with experience and further qualifications.

You can complete a specialized program to gain a certification as a clinical research associate. This can be useful in establishing your career in the industry and can give you a competitive advantage over other applicants. Choosing the right clinical research associate training for your needs will depend on your individual goals and circumstances.

Clinical Research Associate Salary

Every pill, vaccine, therapy or medical device that you take to improve your health goes through a clinical trial. These trials ensure that any potential side effects – both good and bad – are documented. Clinical research associates (CRAs) play a vital role in this process. CRAs work for either a pharmaceutical or medical device company, contract research organization, a university department or physician office.

To become a CRA, you need at least a bachelor’s degree in a health-related field. This can include degrees in health sciences, nursing, medical technology or biological science. Some CRAs also pursue a postgraduate qualification. This may give them an advantage when applying for senior positions or advancing into protocol development.

While a postgraduate qualification is not essential, it can make you stand out to employers and improve your salary. In addition, gaining a certification from the Association of Clinical Research Professionals (ACRP) is a great way to demonstrate your skills and experience.

clinical research associate jobs

Clinical Research Associate Jobs

Every pill, vaccine, device or therapy that improves health conditions undergoes clinical research trials before it gets on the market. These trials ensure that new products are safe and effective, and are not likely to cause side effects. Clinical research associates (CRAs) oversee the trials and work in pharmaceutical labs or contract research organisations. CRAs also work for hospitals and private clinics. They may have to travel between sites.

A day in the life of a CRA revolves around setting up and monitoring trials, ensuring that all equipment is labelled and tagged, and recording all procedures for future reference. Occasionally they are required to close down trials at site and sometimes this requires international travel.

The qualifications for becoming a CRA include a degree or equivalent work experience and a good understanding of the ICH guidelines. Those without a degree can gain experience by working as an LPN, LVN or RN and can progress to the role with additional training. Some companies will even hire someone straight out of high school for a position as an admin assistant or data coordinator to get them started on the career path.

Clinical Research Associate Entry Level

If you want to become a clinical research associate (CRA), you need to have a bachelor’s degree in a health science-related field. You can also pursue a master’s degree, which may make you more competitive in the job market. In addition, you should participate in clinical research projects to gain experience.


CRAs monitor the progress of clinical trials and ensure that they meet quality standards. They perform a variety of tasks, including screening and assessing potential trial participants, preparing sites for the study, stocking supplies, and recording data. They also conduct in-person or virtual site visits to verify that the research is meeting its goals.

CRAs are a vital part of the clinical trials process and work in many different areas of medicine. Depending on the company, they might work for a pharmaceutical or biotechnology firm or a medical consulting firm. Some CRAs even work for a hospital. A good way to get started in the field is by enrolling in a CRA academy. The CRA Academy’s comprehensive ICH-Good Clinical Practice E6 R2 training can help you learn and develop your skills in clinical monitoring.

Clinical Research Associate Resume

A clinical research associate (CRA) works independently of the sponsor’s investigative staff, monitoring studies based on a clinical trial monitoring plan. They collect and analyze data, oversee regulatory compliance, and conduct site visits in person or remotely. Some CRAs work for companies that specialize in medical research, while others are employed by universities or government agencies.

A strong clinical research associate resume objective highlights your professional qualifications, including the ability to work as part of a team and your commitment to advancing medical science through research initiatives. It also emphasizes your dedication to making a difference in patients’ lives. It should include a detailed list of your work experience in a related field and any professional certifications or specializations you have earned.

A CRA resume should start with your education section, which includes any degrees you have earned and the name of the university from which you graduated. You should also include any additional training programs or continuing education courses that relate to your job responsibilities. If you have a specialty certification, be sure to include the name of the organization and the year in which you received it.

clinical research associate training

Clinical Research Associate Training

Whether you should pursue certification as a Clinical Research Associate depends on your individual goals and interests. CRAs are in demand and have many opportunities for advancement. However, it’s important to understand what certifications are available and how they differ from one another. A CRA certification shows employers that you have met specific requirements for working in the field of clinical research.

Training for a Clinical Research Associate is provided by a variety of sources. Some large contract research organizations will train an inexperienced graduate into a monitoring role and provide on-the-job training, while hospitals often recruit graduates into their clinical trials departments. Specialist recruitment agencies also handle CRA vacancies.

A CRA requires excellent organizational and communication skills, and a strong understanding of the clinical trial process and regulations. They must also have excellent attention to detail and be able to work independently. They may be required to travel to clinical trial sites, and should have a clean driving licence for this purpose. Having a relevant undergraduate degree is essential, but postgraduate qualifications are not necessary.

CCRA Community VA

If you want to advance your career in clinical research, consider getting certified as a CCRA. There are several options for obtaining your certification, including taking a course, attending study sessions, or studying on your own. The CRA exam is difficult, and you should prepare for it by studying several hours each week. You can also participate in weekly webinars to discuss subject matters that may appear on the exam.


FTC will continue its support of the Community Care Referrals and Authorizations (CCRA) system, an automated solution that generates referrals and authorizations for veterans receiving community care services. This five-year, $217 million contract includes one base year and four option years.

The CCRA system is a commercial off-the-shelf software solution hosted on Amazon Web Services GovCloud. It interfaces with VA systems to enable bi-directional exchange of appointment data and is rated FedRAMP FISMA High. The system has already generated more than ten million community care referrals and authorizations, saving both time and resources for Veterans and VA community care staff.

Clinical Research Associate Near Me

To become a clinical research associate (CRA), you need to have at least a bachelor’s degree in life sciences or medical sciences. It’s also possible to get into the career with a higher national diploma (HND), but this is unlikely to make you eligible for clinical trials work. Large contract research organisations may hire inexperienced graduates into a monitoring role and provide the training to progress to a CRA position. Hospital academic departments also occasionally employ CRAs within their clinical trials units.

CRAs monitor clinical studies conducted by pharmaceutical companies and medical research institutes, and ensure that the trials adhere to Good Clinical Practice (GCP) guidelines. They also perform a number of other duties, including coordinating project meetings and writing visit reports.

To advance in the career, you can pursue a master’s degree program to qualify for management roles or increase your salary. The following are the most common skills that employers expect Clinical Research Associates to have. We’ve also included the percentage of job postings that request each skill and the marginal value of having it.

Clinical Research Associate Questions and Answers

Clinical research associates often organize clinical trials for research centers, clinical agencies, and pharmaceutical corporations. They collaborate closely with other clinical research experts to evaluate novel medications, techniques, and biotechnologies that might improve current medical procedures and patient conditions. Their responsibility is to assess the trial’s possible dangers and consult with other experts to choose the appropriate safety precautions.

In order to offer study or trial results, they could also be in charge of developing and maintaining agreements with data management facilities.

A clinical research associate (CRA), often known as a clinical monitor or trial monitor, is a health care practitioner who manages a variety of tasks for clinical trials and other types of medical research. Clinical research associates are employed by a variety of organizations, including pharmaceutical firms, hospitals, and governmental organizations.

An associate in clinical research makes, on average, $79,359 per year. This compensation is subject to change based on the size and location of the organization. Be sure to verify with other businesses in your area before determining a competitive wage for your Clinical Research Associate.

A CRA needs to be self-motivated and possess strong core principles in order to handle the day-to-day responsibilities and challenges of the role in a field where transparency and ethics are paramount.

Finding honest and qualified clinical research associates (CRAs) has taken on a new relevance within the business as recruiters and hiring directors for clinical research organizations (CROs) detect a sharp rise in the amount of fraudulent applications for open positions.

If you want to advance your career and challenge yourself, clinical research is a great field to work in. At ICON, we take that responsibility very seriously. There is a shortage of CRAs, but there is no shortage of talent ready to be taught. The norm in the industry is that you need two years of experience inside the sector to work as a Clinical Research Associate (CRA) and supervise tests.

Every step of the clinical monitoring and site management process is carried out and coordinated by a senior clinical research associate. They plan, carry out, and keep an eye on clinical experiments.

Clinical research associates (CRA) are essential to the healthcare sector and the advancement of public health. They serve as the intermediaries between individuals who support clinical research and those who sponsor it. Rising population density and international travel have accelerated the spread of both new and old diseases even before the COVID-19 pandemic. Gaining evidence-based insights on how well a medicine or vaccination performs requires clinical research.

  1.  Study for a bachelor’s degree in a field connected to health sciences. Candidates for clinical research associate roles often need a bachelor’s degree in a discipline relevant to health sciences. 
  2. Gain experience Most firms prefer candidates with prior experience in the industry when hiring entry-level employees for clinical research employment. By seeking for part-time jobs in a lab or clinic, you can gain expertise. 
  3. Think about getting a master’s in a discipline linked to health sciences. Consider pursuing a master’s degree in a topic connected to health sciences if you believe you might want to work in management or supervision in the future. 
  4. Think about certification You could pursue certification as a Certified Clinical Research Associate (CCRA), which the Association of Clinical Research Professionals offers, after gaining some experience as a clinical research associate.

Yes, it is possible for Clinical Research Associates (CRAs) to work from home, especially in certain circumstances or during specific stages of a clinical trial. However, it’s important to note that the extent of remote work opportunities may vary depending on the specific requirements and nature of the trial, as well as the policies of the sponsoring organization or contract research organization (CRO).

Yes, Clinical Research Associates (CRAs) often travel as part of their job responsibilities. Travel is a significant component of a CRA’s role, especially during the monitoring phase of clinical trials. The extent of travel can vary depending on factors such as the geographic scope of the trial, the number of investigational sites involved, and the duration of the study.

As of May 25, 2023, the average Senior Clinical Research Associate wage in the United States is $106,951, although the normal salary range is between $93,125 and $122,519. Salary ranges can vary significantly depending on a variety of crucial aspects, including schooling, credentials, supplementary talents, and the length of time you’ve been working in a given field.

You must pass the CRAC credentialing exam in order to become a certified Canadian CRA. You must meet one of the following conditions in order to register for the test:

  • 2 years of recent experience conducting clinical research 
  • 3,500 part-time hours, with at least a year of experience in Canada during the previous five years. 
  • A post-graduate certificate in clinical research and at least one year’s worth of experience in clinical research over the previous two years. You need to have worked in Canada for at least a year.

Complete 1,500 hours of equivalent work experience or 3,000 hours executing key job functions through eligible clinical research degree programs certified by the Council for Higher Education.