- Recognize, exemplify and adhere to ICON's values which center around our commitment to People, Clients and Performance.
- As a member of staff, the employee is expected to embrace and contribute to our culture of process improvement with a focus on streamlining our processes adding value to our business and meeting client needs.
- Perform genetic and molecular biology laboratory procedures involving traditional techniques such as PBMC, isolation of DNA and RNA, PCR, RT-PCR, Real-Time PCR, and other molecular techniques (knowledge of Illumina MiseqDx NGS and Luminex 200 are strongly desired)
- Operate equipment carefully and according to procedures; maintain laboratory automation equipment per established operating procedures.
- Perform necessary equipment checks, performance testing, preventive maintenance, and quality control on equipment per laboratory guidelines, as assigned.
- Assure equipment and instruments meet performance standards.
- Maintain QC related documents.
- Assure the accuracy of all tests performed by adhering to the laboratory’s Quality Control Standard Operating Procedures.
- Maintain complete documentation for assay tracking and results for review/reporting.
- Participate in the Proficiency Testing Program as assigned.
- Complete the performance of proficiency testing in assigned laboratory sections.
- Review all test requests thoroughly for errors, omissions, clarity, and potential problems.
- Verify patient identification at all steps of every procedure and maintain complete accuracy.
- Follow unidirectional flow of specimen handling to avoid contamination.
- Notify supervisor of discrepancies and records corrective action taken.
- Help maintain commonly used equipment and resolve minor equipment problems. Troubleshoot instrument related issues as they occur.
- Strong interpersonal and communication skills.
- Good laboratory and organizational skills, including the ability to work independently and efficiently are essential.
- Ability to multitask, along with an orientation toward teamwork and leadership.
- Strong creative thinking and problem solving skills.
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BlogsPublish date
05/07/2025
Summary
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IndustryContent type
BlogsPublish date
05/05/2025
Summary
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IndustryContent type
BlogsPublish date
04/22/2025
Summary
What is an IND or NDA? A Guide for Aspiring Clinical Research Professionals If you’re considering a career in clinical research or the broader pharmaceutical and biotech industry, you’ve likely c
Salary
Location
Taipei
Department
Clinical Trial Management
Location
Taipei
Remote Working
Office Based
Job Categories
Clinical Trial Management
Job Type
Permanent
Description
Jot Title: Site Care PartnerWorking location: client office based (Flexible WFH)Sponsor: Top 10 Global pharma ICON plc is a world-leading healthcare intelligence and clinical research organization. We
Reference
2025-119251
Expiry date
01/01/0001
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Salary
Location
Beijing
Department
Clinical Monitoring
Location
Beijing
Job Categories
Clinical Monitoring
Job Type
Permanent
Description
As a Clinical Research Associate you will be joining the world’s largest & most comprehensive clinical research organisation, powered by healthcare intelligence.
Reference
2025-117161
Expiry date
01/01/0001
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Salary
Location
Guangzhou
Department
Clinical Monitoring
Location
Guangzhou
Job Categories
Clinical Monitoring
Job Type
Permanent
Description
As a Clinical Research Associate you will be joining the world’s largest & most comprehensive clinical research organisation, powered by healthcare intelligence.
Reference
2025-117160
Expiry date
01/01/0001
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Salary
Location
Mexico
Department
Regulatory, Drug Safety/ Quality Assurance & Other roles
Location
Mexico
Remote Working
Remote
Job Categories
Other
Job Type
Permanent
Description
As a Senior Feasibility Specialist you will be joining the world’s largest & most comprehensive clinical research organisation, powered by healthcare intelligence.
Reference
2025-119242
Expiry date
01/01/0001
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Salary
Location
United States
Department
Clinical Trial Management
Location
United States
Remote Working
Remote
Job Categories
Clinical Trial Management
Job Type
Permanent
Description
As a Senior Clinical Study Lead, you will be joining the world’s largest & most comprehensive clinical research organisation, powered by healthcare intelligence.
Reference
2025-119201
Expiry date
01/01/0001
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Salary
Location
Canada
Department
Clinical Monitoring
Location
Canada
Remote Working
Remote
Job Categories
Clinical Monitoring
Job Type
Permanent
Description
The Study Start Up CRA is accountable for site selections as well as study specific start up activities and deliverables of assigned sites for Phase I-IV trials in the country in accordance with monit
Reference
2025-119257
Expiry date
01/01/0001
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