Description

Clinical research associates (CRA) are accountable to assist in the process of conducting clinical research, offering advanced technical assistance in areas such as handling equipment, ordering tests, and presenting results, specific research data to the general public, and various administrative tasks. CRAs must adhere to strict safety and privacy regulations to avoid problems with their subjects and ethical concerns They must also organize themselves and give careful attention to the finer points when conducting research using investigative techniques in healthcare or clinical settings.

Communication skills are essential for this job to build strong relationships with business partners and multitasking abilities are essential to complete documents and maintain research records to be able to refer back later. They can collaborate with other teams to achieve targets within strict deadlines, however, they should be able to work independently with little supervision. CRAs should be adept with computers to record research data and complete applications, documents, and other data that is required and also Microsoft Office applications to write comprehensive reports based on their research findings. They also make use of electronic communications to collect information.

Research associates in clinical research work within offices or lab environments based on the company, and must be able to stand in a position for extended durations of time. They should be skilled in research and know how to utilize equipment and tools for research and also perform maintenance and cleaning services even when they are not using. High school graduation is needed for this job, and previous experience in the field of clinical research is extremely beneficial. Research certificates are also beneficial.

Roles & Responsibilities

As a Clinical Research Associate CRA with 0-3 years of experience in the United Kingdom, your main responsibilities include:

  • Assisting in the coordination and execution of clinical trials, ensuring compliance with all applicable regulations and guidelines.
  • Collecting and verifying data from study sites, ensuring accuracy and completeness.
  • Conducting site initiation, monitoring, and close-out visits to ensure protocol adherence and patient safety.
  • Collaborating with cross-functional teams, including investigators, sponsors, and regulatory authorities, to ensure efficient and successful study implementation.

Qualifications & Work Experience

For a Clinical Research Associate (CRA) job role, the following qualifications are required:

  • Bachelor's degree in a relevant scientific field such as biology, pharmacology, or clinical research.
  • Strong knowledge and understanding of the clinical research process, including regulatory guidelines and good clinical practice (GCP) standards.
  • Excellent attention to detail and the ability to meticulously collect, record, and analyze clinical trial data accurately and efficiently.
  • Effective communication and interpersonal skills to collaborate with cross-functional teams, investigators, and study participants, ensuring smooth coordination and adherence to protocol requirements.

Essential Skills For Clinical Research Associate (CRA)

1

Data Management

2

Clinical Research

3

Verbal Communication

4

Data Analysis

5

Medical Technology

Skills That Affect Clinical Research Associate (CRA) Salaries

Different skills can affect your salary. Below are the most popular skills and their effect on salary.

Clinical Research

1%

Healthcare Operations

3%

Monitoring Data

4%

Career Prospects

The Clinical Research Associate CRA plays a crucial role in the healthcare industry. For individuals with 0-3 years of experience in the field in the United Kingdom, there are several alternative roles to consider. Here are following options:

  • Clinical Trial Coordinator: Assisting in the coordination and administration of clinical trials, working closely with investigators, sponsors, and regulatory bodies.
  • Data Manager: Responsible for collecting, organizing, and managing clinical trial data, ensuring accuracy and compliance with regulatory guidelines.
  • Regulatory Affairs Associate: Supporting the preparation and submission of regulatory documents, ensuring compliance with applicable laws and regulations.
  • Clinical Research Administrator: Assisting in the administrative aspects of clinical trials, maintaining study documentation, and coordinating communication among stakeholders.

How to Learn

The job role of a Clinical Research Associate (CRA) in the United Kingdom is projected to experience significant growth in the market. Over the past 10 years, the demand for CRAs has steadily increased due to the expansion of the pharmaceutical and healthcare industries. This trend is expected to continue, with a positive outlook on the availability of future employment opportunities. According to recent data from Google, the number of job openings for CRAs in the UK is expected to rise in the coming years, reflecting the growing need for professionals in this field.