Description

Clinical research associates (CRA) are responsible for assisting in the clinical research process, providing advanced technical expertise in steps such as handling supplies, ordering tests, and collecting results, presenting specific research information to the public, and a variety of administrative tasks. CRAs must follow strict privacy and safety regulations to prevent problems with subjects and ethical concerns; they must also be organized and pay close attention to detail when conducting research using investigative methods in clinical or healthcare settings.

Excellent communication skills are important in this position in order to develop strong business relationships, and multitasking skills are important to complete paperwork and keep research records for future reference. They may work in teams to reach goals under strict deadlines, but should also work well on their own with minimal supervision. CRAs must be proficient with computers to log research information and fill out applications, documents, and other required data, as well as Microsoft Office applications to write detailed reports based on their findings. They also use electronic communication to gather information.

Clinical research associates work in offices and laboratory environments depending on the employer, and should be able to stand on their feet for long periods of time. They must be highly skilled in research and how to use research tools and equipment, as well as provide maintenance and cleaning functions when not in use. A high school diploma is required for this position, and prior work experience in a clinical research capacity is highly beneficial. Research certifications are also helpful.

Roles & Responsibilities

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

  • Conducting site initiation visits, ensuring ethics committee approvals, and collecting regulatory documents.
  • Performing site qualification visits, assessing investigators' capabilities, and ensuring site compliance with protocols and regulations.
  • Monitoring clinical trial activities, including source data verification, adherence to protocol, and reporting adverse events.
  • Coordinating and maintaining study documentation, including study binders, regulatory files, and study tracking systems.

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

Clinical Research

2

Healthcare Operations

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

4%

Healthcare Operations

13%

Career Prospects

For a Clinical Research Associate CRA with 0-3 years of work experience in Singapore, various alternative roles can be considered. Here are following options to explore:

  • Clinical Trial Coordinator: An entry-level role that involves supporting the coordination and administration of clinical trials, ensuring compliance with protocols and regulatory guidelines.
  • Data Management Associate: A role focused on collecting, managing, and analyzing clinical trial data, ensuring accuracy and integrity throughout the process.
  • Regulatory Affairs Assistant: A position that involves assisting with the preparation and submission of regulatory documents, ensuring compliance with applicable regulations and guidelines.
  • Quality Assurance Specialist: A role focused on ensuring compliance with Good Clinical Practice GCP guidelines, conducting audits, and implementing quality control measures in clinical research processes.

How to Learn

The job role of Clinical Research Associate (CRA) in Singapore is projected to experience significant growth in the market. Over the past 10 years, the demand for CRAs has been rising steadily, with a positive trend expected to continue in the future. According to recent data, the employment opportunities in this field are expected to increase substantially. The projected growth reflects the expanding pharmaceutical and healthcare sectors in Singapore, as well as the growing importance of conducting clinical trials in the region. This upward trajectory indicates promising prospects for individuals pursuing careers as Clinical Research Associates in Singapore.