Description

Clinical research coordinators (CRC) are in charge of coordinating clinical and administrative tasks in the research process on behalf of their organization. They attend to participants' questions and respond with details related to clinical steps as needed. Clinical research coordinators are responsible for collecting and organizing research data for future analysis, as well as performing appropriate research protocol procedures (such as taking vital signs, collecting and processing blood, and performing other necessary tasks).

Additionally, clinical research coordinators use a personal computer to keep accurate records of research participants, and detailed notes about the research process. They are also in charge of maintaining and dispensing clinical research product and supplies. Their main responsibilities also include managing and participating in study recruitment to ensure enrollment goals are met or exceeded. They need to be proficient with office applications to communicate with other research staff. These coordinators also conduct the informed consent process and monitor patient status, following all safety and privacy procedures.

A high school diploma or equivalent is generally required for this job. In addition, previous experience in a clinical research capacity is generally needed as well. Industry certifications may be beneficial. hey are organized individuals that pay close attention to detail. Clinical research coordinators must be well organized, have excellent communication skills, and be able to work with colleagues to reach all company objectives in a timely manner. They also need to perform effectively on their own with minimal supervision. Coordinators also need to have excellent organizational and time-management skills and be able to multitask on a variety of research projects.

Roles & Responsibilities

As a Clinical Research Coordinator CRC in Singapore with 3-6 years of experience, your main responsibilities include:

  • Oversee the planning and execution of clinical trials, ensuring compliance with protocols, regulations, and ethical guidelines.
  • Coordinate with investigators, study sponsors, and healthcare professionals to recruit and enroll eligible participants for research studies.
  • Manage and maintain accurate documentation and records of study protocols, participant data, adverse events, and regulatory submissions.
  • Collaborate with multidisciplinary teams to monitor study progress, evaluate data quality, resolve queries, and ensure timely completion of research projects.

Qualifications & Work Experience

For a Clinical Research Coordinator (CRC) job role, the following qualifications are required:

  • Bachelor's degree in a relevant field such as biology, chemistry, or health sciences.
  • Strong understanding of Good Clinical Practice (GCP) guidelines and regulatory requirements for clinical trials.
  • Excellent organizational and multitasking skills to effectively manage multiple research projects simultaneously.
  • Proficiency in data collection and analysis, including experience with electronic data capture (EDC) systems and statistical software.

Essential Skills For Clinical Research Coordinator (CRC)

1

Clinical Research

2

Clinical Study Reports

3

Research and Analysis

4

Reporting

Career Prospects

With 3-6 years of experience as a Clinical Research Coordinator CRC in Singapore, there are several alternative roles for professionals to consider. Here are following options to explore:

  • Clinical Research Associate CRA: A position that involves monitoring and managing clinical trials, ensuring compliance with regulatory requirements, and collecting and analyzing data.
  • Project Manager: A role focused on overseeing and coordinating clinical research projects, including budget management, timeline adherence, and team coordination.
  • Data Manager: A position that involves the collection, organization, and analysis of clinical trial data, ensuring data integrity and accuracy.
  • Regulatory Affairs Specialist: A role that involves ensuring compliance with regulatory guidelines and requirements, preparing and submitting documentation to regulatory authorities, and liaising with cross-functional teams.

How to Learn

The role of Clinical Research Coordinator (CRC) in Singapore is projected to witness significant growth in the job market. According to a 10-year analysis, employment opportunities for CRCs are expected to increase steadily. With advancements in medical research and increasing demand for clinical trials, the need for CRCs is likely to expand. The growing emphasis on evidence-based medicine and regulatory requirements in the healthcare industry further supports this trend. Based on the latest data points available from Google, it can be concluded that there will be ample employment opportunities for CRCs in the future, making it a promising career choice in Singapore.