Investigator Services Assistant (Korean/Japanese)
at Thermo Fisher Scientific
Singapore 637431, Central, Singapore -
Start Date | Expiry Date | Salary | Posted On | Experience | Skills | Telecommute | Sponsor Visa |
---|---|---|---|---|---|---|---|
Immediate | 21 Nov, 2024 | Not Specified | 22 Aug, 2024 | N/A | Interpersonal Skills,Software,Databases,Data Flow | No | No |
Required Visa Status:
Citizen | GC |
US Citizen | Student Visa |
H1B | CPT |
OPT | H4 Spouse of H1B |
GC Green Card |
Employment Type:
Full Time | Part Time |
Permanent | Independent - 1099 |
Contract – W2 | C2H Independent |
C2H W2 | Contract – Corp 2 Corp |
Contract to Hire – Corp 2 Corp |
Description:
JOB REQUIREMENTS:
- Proven experience in a similar role within the clinical research industry.
- Exceptional attention to detail and ability to ensure flawless data flow.
- Strong communication and interpersonal skills to effectively liaise with sites, monitors, and internal departments.
- Ability to triage and resolve issues promptly and efficiently.
- Understanding of study protocols and pre-analytical requirements.
- Highly organized with the ability to manage multiple tasks and prioritize effectively.
- Proficient in using databases and software for data management.
- Fluency in Korean and Japanese languages.
- Ability to work collaboratively in a team environment.
- Ambitious and self-motivated, with a drive to compete and succeed.
Responsibilities:
- Act as the main point of contact for sites and monitors, ensuring timely resolution of complaints, concerns, and discrepancies.
- Communicate with sites regarding protocol-related aspects, providing guidance on pre-analytical study requirements.
- Triage calls and redirect them to the appropriate department for resolution.
- Review and resolve exceptions to ensure data cleaning within agreed timelines.
- Resolve queries to facilitate efficient sample analysis and meet report turnaround time.
- Notify sites and relevant contacts of critical values and study-specific requirements.
- Monitor and report site issues to the relevant departments for resolution.
- Evaluate requests for additional tests and inform investigator sites of the results or reasons for not proceeding.
- Coordinate and resolve issues with samples and requisition forms for timely accessioning and reporting.
- Amend patient information in the site database as required.
- Attend study meetings to discuss risk assessment and business concerns.
- Collaborate with the study PM team to create requisition forms capturing visit and study collection requirements.
REQUIREMENT SUMMARY
Min:N/AMax:5.0 year(s)
Information Technology/IT
Pharma / Biotech / Healthcare / Medical / R&D
Software Engineering
Graduate
Proficient
1
Singapore 637431, Singapore