• Our Client is a well-established Healthcare Organization.

Responsibilities: 

Research Administration

• Recruitment of ward patients for participation in the clinical trial.
• Preparation, organisation and submission of documents required for research ethicsgovernance.
• Project management and coordination with research collaboration partner.
• Translation of research materials.
• Development of scientific papers and dissemination of study findings.

Data Collection and Analysis

• Record videos of the trial participants interacting with the robot and coding the videorecordings.
• Interviewing and taking clinical measurements of trial participants.
• Case note review.
• Conduct quantitative/qualitative analysis under the supervision of senior researchers.

Requirements:

• Bachelor’s Degree in Social Science (e.g. Psychology, Sociology).
• At least 2 years’ relevant working experience in Health-related research project.
• Excellent communication skills, both verbal and written.
• Ability to work independently and within a multidisciplinary team.
• Ideally have prior experience of reading/extracting data from electronic medical records.
• Evidence of publication is desirable.
• Prior experience of applying for ethical review is desirable.

Other Information:

• Six (6) Months' Contract.
• Working Location: West.
• Working Hours: Mondays to Fridays, 8.30am to 5.30pm.
• Critical: Due to the organization's affirmed support and commitment to developing a Singaporean core, this role is only available to Singaporeans.

To apply, please visit www.gmprecruit.com and search for Job Reference: 17922.
To learn more about this opportunity, please contact Novita Tan at novita.tan@gmprecruit.com
We regret that only shortlisted candidates will be notified.
GMP Recruitment Services (S) Pte Ltd | EA License: 09C3051 | EA Personnel: Novita Tan | Registration No: R1220374