Clinical Research Nurse — Patient-Centric Trial Support

Recruit Express Pte Ltd; Singapore; Presencial; SGD 42 000 - 65 000; Tempo integral

Resumo da oferta

Recruit Express Pte Ltd in Singapore is seeking a Nurse to provide clinical support within a research team. You will screen and recruit patients, brief them on study background, and obtain informed consent in line with protocols.

You will collect and document data from medical records and research sources, assist with data statistics, monitor adverse events, and perform phlebotomy when required. Prior research exposure is advantageous.

Qualificações

• Minimum Diploma or Degree in Nursing.
• At least 3 years hospital nursing experience.
• Strong clinical knowledge and patient-care skills.
• Good communication and interpersonal skills.
• Detail-oriented with good documentation skills.
• Able to work independently and as part of a research team.
• Relevant clinical research experience is an advantage.
• Prior experience in cannulation and drawing blood.

Responsabilidades

• Provide nursing and clinical support to the research team.
• Screen and recruit suitable patients to participate in research projects.
• Brief patients on the research background, objectives, and rationale.
• Obtain informed consent from patients in accordance with research protocols.
• Collect and document relevant data from patients' medical records and research records.
• Assist with the collection and documentation of research statistics and study data.
• Monitor and document any adverse events or reactions that may arise during the study.
• Perform phlebotomy and venepuncture when required.
• Perform other clinical and research-related duties as assigned.

Conhecimentos

Nursing

Phlebotomy

Clinical data collection

Informed consent

Documentation

Communication skills

Team collaboration

Formação académica

Diploma or Degree in Nursing

Descrição da oferta de emprego

Recruit Express Pte Ltd in Singapore is seeking a Nurse to provide clinical support within a research team. You will screen and recruit patients, brief them on study background, and obtain informed consent in line with protocols.

You will collect and document data from medical records and research sources, assist with data statistics, monitor adverse events, and perform phlebotomy when required. Prior research exposure is advantageous.