Clinical Research Coordinator (CRC)

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.

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

• Assist in managing clinical research projects, ensuring adherence to regulatory and ethical guidelines while maintaining accurate documentation. Help in overseeing the progress of clinical research studies, following established protocols, and ensuring compliance with regulatory standards.
• Collaborate with principal investigators, sponsors, and clinical trial teams in coordinating and organizing study activities. Work closely with research teams to facilitate smooth operation of clinical trials, coordinating tasks and ensuring effective communication among stakeholders.
• Recruit study participants and facilitate informed consent process, ensuring proper procedures are followed. Play a key role in identifying and enrolling eligible participants, explaining study details, obtaining consent, and ensuring participant safety throughout the research process.
• Collect and analyze research data, maintain accurate records, and assist in preparing reports for regulatory submissions.

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.

The role of a Clinical Research Coordinator CRC is crucial in managing clinical trials and ensuring smooth operations. With 0-3 years of experience in Singapore, here are following alternative roles to consider:

• Clinical Research Associate CRA: A position that involves monitoring and overseeing clinical trials, ensuring adherence to protocols and regulatory guidelines.
• Data Manager: A role focused on managing and analyzing clinical trial data, ensuring accuracy, and maintaining data integrity.
• Regulatory Affairs Coordinator: A position involved in preparing and submitting regulatory documents, ensuring compliance with local and international regulations.
• Clinical Trial Assistant: A role that supports CRCs in administrative tasks, such as organizing study documents, coordinating meetings, and maintaining trial databases.

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.