Clinical Research Assistant

QA Employment Consultant

Clinical Research Assistant

For a MNC company

-5 working days
-Attractive remuneration
-Attractive company benefits
-Attractive Bonus

Job Descriptions:

– Assist Clinical Research Manager (CRM) with the identification and selection of investigators to undertake clinical studies, when required.
– Assist the CRM in preparing study budget.
– Prepare documentation for Ethics Committee submission.
– Coordinate receipt and distribution of clinical trial supplies.
– Liaise with various parties (investigators, site staff, vendors) to coordinate timely set up of study logistics and initiate studies.
– Prepare and conduct initiation visits.
– Implement appropriate monitoring tools.
– Monitor and document the progress of assigned clinical studies through regular visits and telephone contact with site personnel.
– Communicate effectively with global and local study managers, fellow CRAs, and country office colleagues from other departments

– Perform quality control/monitoring visits to ensure:
– Documentation of investigator contacts and all study related communications.
– Maintain drug accountability of all clinical supplies and arrange for destruction as per specified clinical study.
– Perform Source Data Verification to ensure accurate data is recorded.
– Liaise effectively with investigators and site staff to train, troubleshoot and drive patient recruitment
– Ensure that Serious Adverse Event Reports are reviewed and reported in accordance to timelines.

– Ensure study documentation for each clinical trial is complete in accordance with set schedules.
– Assist CRM to track study payments to ensure payments are on time and within budget.
– Review and prepare study reports for regulatory agency when required.
– Timely and accurate completion of Monitoring visit reports.
– Ensure regular updating of Clinical Research tracking systems, every month.
– Prepare monthly study progress reports for CRM or other project team members by specified dates.
– Meet as required with CRM to discuss ongoing performance and development, and CSM to identify, discuss and resolve study issues and determine priorities and timelines.

Job Requirements

-Minimum Degree in Biomedical, Pharmaceutical or relevant
-Minimum 2 years of experience in the research related positions
-Excellent coordination and time management skills
-Excellent Team player

To apply, please email resume to
For more information, Please call 6337 7449

(Wong Yen Yong Christine, EA Registration No: R1101725)

To apply for this job please visit

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