Long-Term Clinical Study Assistant (Part time, Up to $14/hr) #HCK

RECRUIT EXPRESS PTE LTD; Singapore; On-site; SGD 17,000 - 25,000; Part time

Job summary

RECRUIT EXPRESS PTE LTD in Singapore is seeking a part-time research support staff to assist with day-to-day clinical study activities, perform ECGs on participants, obtain informed consent, and help manage samples and study documentation. This long-term, 5-day-per-week role is based at Buona Vista and offers hands-on experience in clinical research, including health screening procedures and data entry.

Applicants with healthcare or clinical research exposure, good attention to detail, and a

Qualifications

• > Healthcare, clinical research, nursing, or allied health background is advantageous.
• "> Able to follow study protocols with good attention to detail.
• "> Good organizational and communication skills; team-oriented.

Responsibilities

• > Support research projects and assist with day-to-day clinical study activities.
• "> Perform ECGs on research study participants.
• "> Obtain informed consent from research participants before procedures.
• "> Handle, process, and preserve biological samples per protocols.
• "> Perform data entry and data quality checks of study forms and reports.
• "> Maintain clinical inventory, equipment, and study supplies.
• "> Conduct health screening procedures and surveys.
• "> Train and assess staff in health screening procedures and surveys.
• "> Assist with everyday operation of research projects.
• "> Assist with other clinical and administrative duties related to research studies.

Skills

ECG procedures

Data entry

Health screening

Communication

Job description

Location: Buona Vista, Singapore

Working Schedule: 5 days per week

Salary: $14 per hour

Employment: Long-term Part time

Job Responsibilities

• Support research projects and assist with day-to-day clinical study activities.
• Perform ECGs on research study participants.
• Obtain informed consent from research participants before carrying out research procedures.
• Properly handle, process, and preserve biological samples in accordance with study protocols.
• Perform accurate data entry and data quality checks (QC) of study forms, reports, and related documentation.
• Maintain clinical inventory, equipment, and study supplies.
• Conduct health screening procedures and surveys according to established protocols.
• Train and assess staff in performing health screening procedures and surveys.
• Assist in ensuring the smooth, efficient, and productive operation of research projects.
• Assist with other clinical and administrative duties related to research studies as required.

Requirements

• Relevant qualifications or experience in healthcare, clinical research, occupational therapy, nursing, allied health, or a related field will be an advantage.
• Comfortable interacting with research participants and working as part of a team.
• Good attention to detail and ability to follow clinical study protocols accurately.
• Good organizational and communication skills.
• Willingness to learn and perform clinical procedures such as ECG and health screening.
• Previous clinical research experience is an advantage but not essential.

Why Join Us?

• Long-term employment opportunity
• Structured 5-day work week
• Hands-on experience in clinical research
• Opportunity to develop skills in clinical procedures, research operations, and participant management
• Convenient location at Buona Vista