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Recognize, exemplify and adhere to ICON's values which centres around our commitment to People, Clients and Performance
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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.
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Must make and document scientific observations and identify and solve problems in experimental designs independently
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Keeps manager and Project Leaders informed of study status, technical problems and other issues which impact the laboratory
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Independently interprets data to solve practical problems and isolate variables in situations where troubleshooting problematic assays or unanticipated failures is required and proposes next steps including implementation of effective CAPA.
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Advises and supports more junior scientists and the laboratory managers and project leaders when deviations or factors at may affect quality, accuracy and usefulness of the data occurs.
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The desire and ability to document results of test samples that include performing statistical analyses, identifying repeats or next trier analysis needs based on SOPs and other guiding documents.
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Document all work and results accurately, completely and in compliance with GXP regulations and SOPs.
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Plans daily, weekly and monthly activities based on goals and timelines established by supervisor for scheduled projects
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Work in compliance with Study Plans and validation plans.
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Generate high quality analytical results.
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Designs, directs and participates in equipment (and software) validations/calibration/maintenance as necessary
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Participates in internal seminars and poster sessions, and local and regional scientific meetings in own field as necessary to continue professional development and to distribute such knowledge to colleagues
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Assist in training new staff members in performance of routine lab tasks, methods and instruments
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Develops and mentors less experience lab members – encourages growth and provides regular performance feedback to staff and management
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Responsible for participating in the design, execution and review of the on-boarding and training process
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To perform this job successfully, an individual must be able to perform each essential duty satisfactorily. The requirements listed below are representative of the knowledge, skill, and/or ability required. Reasonable accommodations may be made to enable individuals with disabilities to perform the essential functions.
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Good verbal and written communication skills
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Ability to work independently on routine analysis.
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Strong computer skills (Microsoft Word, Excel, Access and Power Point).
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Ability to undertake tasks with minimal supervision.
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Good organizational skills and record keeping ability.
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Strong attention to detail
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Minimum 3 years lab based biotechnology/biology/chemistry/biochemistry experience
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Bachelor's degree in scientific discipline or local equivalent is preferred
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Salary
Location
China, Shanghai
Location
Guangzhou
Shanghai
Job Categories
Clinical Monitoring
Job Type
Permanent
Description
We are currently seeking a Senior Clinical Research Associate (CRA) to join our diverse and dynamic team. As a Senior CRA at ICON Plc, you will play a critical role in overseeing and managing clinical
Reference
JR129979
Expiry date
01/01/0001
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Salary
Location
China, Guangzhou
Location
Beijing
Guangzhou
Remote Working
Office Based
Job Categories
Clinical Monitoring
Job Type
Permanent
Description
CRA IIResponsibilities:• 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 emb
Reference
JR129957
Expiry date
01/01/0001
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Salary
Location
Australia
Department
Clinical Monitoring
Location
Australia
Job Categories
Clinical Monitoring
Job Type
Permanent
Description
Title: CRA II Location: Australia, Home-based As an experienced Clinical Research Associate, you will be joining the world’s largest & most comprehensive clinical research organisation, powered by hea
Reference
2025-119996
Expiry date
01/01/0001
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Salary
Location
Mexico, Mexico City
Location
Sao Paulo
Santiago
Bogota
Mexico City
Lima
Remote Working
Home or Office
Job Categories
Project Management
Job Type
Permanent
Description
Role Summary:Accountable for driving and accelerating the activation of global investigative sites in line with, or ahead of, the study's contractual timelines, within budgeted resources, with quality
Reference
JR131718
Expiry date
01/01/0001
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Salary
Location
Brazil
Department
Clinical Monitoring
Location
Brazil
Job Categories
Clinical Monitoring
Job Type
Permanent
Description
A Clinical Research Associate is a professional who contributes to accelerated drug/device/outcomes research through independent monitoring of studies to ensure patient safety and data integrity. You
Reference
2025-119866
Expiry date
01/01/0001
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Salary
Location
Mexico City
Department
Regulatory, Drug Safety/ Quality Assurance & Other roles
Location
Mexico City
Job Categories
Other
Job Type
Permanent
Description
We are currently seeking a Manager, Procurement to join our diverse and dynamic team. As a Manager, Procurement at ICON, you will be responsible for overseeing the procurement process, ensuring cost-e
Reference
2025-120103
Expiry date
01/01/0001
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