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

RECRUIT EXPRESS PTE LTD; Singapore; On-site; SGD 40,000 - 60,000; Full time

Job summary

RECRUIT EXPRESS PTE LTD in Singapore is seeking a Clinical Research Coordinator to support investigators in all aspects of clinical studies. You will enrol suitable subjects, take vital signs, collect and process samples, collect data, and enter it into the study database, while liaising with the study team and external agencies to ensure smooth operations.

You will work with the study team to safeguard subjects' safety, perform procedures per SOPs and the ICH-GCP guidelines, and participate in

Qualifications

• Bachelor's degree in sciences, Nursing, Biomedical or related field.
• Diploma may be considered as Associate Clinical Research Coordinators.
• Minimum 2 years of experience coordinating clinical research activities.
• Strong interest in research and good interpersonal & communication skills.
• Familiarity with SOPs, study protocol, instruction manuals and ICH-GCP guidelines.

Responsibilities

• Assist investigators in administration of clinical research before, during and after study.
• Enrol suitable subjects and monitor their condition.
• Take vital signs and collect/process biological samples.
• Collect and enter data, and liaise with internal and external teams during the course of work.
• Attend investigator meetings and site initiation meetings as assigned.

Skills

Clinical coordination

Data entry

Interpersonal communication

Regulatory compliance

Education

Bachelor's degree in sciences

Diploma holder considered

Job description

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