Contract Clinical Study Nurse ( 5 Days Office Hours ) #HCT

RECRUIT EXPRESS PTE LTD; Singapore; In loco; SGD 40.000 - 65.000; Tempo pieno

Descrizione del lavoro

Recruit Express Pte Ltd in Singapore seeks a Clinical Research Coordinator to assist investigators in administration of clinical research activities before, during and after studies, including enrolment of suitable subjects, taking vital signs, collecting data and processing samples.

You will work with the study team to ensure subjects' safety, follow SOPs and ICH-GCP guidelines, attend investigator meetings and liaise with internal and external agencies, performing other duties as assigned.

Competenze

• Bachelor's degree in sciences, Nursing, Biomedical or related discipline.
• Diploma may qualify as Associate Clinical Research Coordinator.
• At least 2 years coordinating clinical research activities.
• Strong interest and passion for research.
• Good interpersonal and communication skills.

Mansioni

• Assist investigators in overall administration of clinical research activities pre, during and post study, including enrolment, vital signs, sample collection and data entry.
• Work with the study team to ensure subjects' safety.
• Follow SOPs, study protocol and ICH-GCP guidelines and regulatory requirements.
• Attend investigator meetings and site initiation meetings; liaise with internal and external agencies.
• Perform other duties as assigned.

Conoscenze

Interpersonal communication

Research interest

Formazione

Bachelor's degree in sciences or related field

Diploma considered as Associate CRC

Descrizione del lavoro

Responsibilities:

• Assist the investigators in overall administration of clinical research activities prior to, during and post study such as enrol suitable subjects, take vital signs, collect and process biological samples, collect and enter data, monitor subjects' condition
• Work with the study team to ensure subjects' safety
• Carry out the required procedures according to the SOP, study protocol and Instruction manual(s) and in compliance with the Regulations and ICH Good Clinical Practice Guideline
• Attend investigator's meeting (local/overseas) and site initiation meeting as assigned and liaise with relevant internal and external agencies during the course of work
• Any other duties assigned from time to time

Requirements:

• Bachelor's degree in sciences, Nursing, Biomedical or any other discipline.
• Diploma will be considered as Associate Clinical Research Coordinators
• 2 years of working experience in coordination of clinical research activities
• Strong interest and passion in research
• Good interpersonal & communication skills