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Data Entry jobs in Malaysia

Clinical Site Associate

ICON Clinical Research

Kuala Lumpur
On-site
MYR 100,000 - 150,000
Yesterday
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Sales & Support Consultant | Mandarin, Cantonese & English

Hunters International Sdn Bhd

Kuala Lumpur
On-site
MYR 150,000 - 200,000
Yesterday
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07 - Customer Program Management Analyst

Celestica

Johor Bahru
On-site
MYR 60,000 - 80,000
Yesterday
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Assistant Executive, Communication and Postal Regulation

Malaysian Communications and Multimedia Commission

Cyberjaya
On-site
MYR 100,000 - 150,000
Yesterday
Be an early applicant

Associate, Continuous Improvement

Celestica Inc.

Kulim
On-site
MYR 100,000 - 150,000
Yesterday
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Sr Layout Engineer

Celestica Inc.

George Town
On-site
MYR 70,000 - 100,000
Yesterday
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Senior Solution Architect/Project Manager SAP EWM, with good command in Mandarin

Sika AG

Kuala Lumpur
Hybrid
MYR 100,000 - 130,000
2 days ago
Be an early applicant

Staff Engineer, Mechanical Design

Celestica Inc.

George Town
On-site
MYR 120,000 - 150,000
Yesterday
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Junior Finance Executive (Accounts Payable)

QCP Group

Kuala Lumpur
On-site
MYR 40,000 - 60,000
Yesterday
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Staff Engineer, Hardware Design

Celestica Inc.

George Town
On-site
MYR 60,000 - 90,000
Yesterday
Be an early applicant

Lead Engineer, CPLD/ FPGA Engineer (HW Design)

Celestica Inc.

George Town
On-site
MYR 100,000 - 130,000
Yesterday
Be an early applicant

Administrator

27 Marketing Sdn Bhd

Puchong
On-site
MYR 100,000 - 150,000
Yesterday
Be an early applicant

Engineer, Manufacturing Process

Celestica

Kulim
On-site
MYR 50,000 - 70,000
Yesterday
Be an early applicant

Senior Manager, Continuous Improvement

Celestica

Kulim
On-site
MYR 120,000 - 150,000
Yesterday
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QC Online Assistant

Two95 International Inc.

Kajang Municipal Council
On-site
MYR 20,000 - 100,000
Yesterday
Be an early applicant

Field Industrial Hygiene Technician

Chemsain Konsultant Sdn Bhd

West Coast Division
On-site
MYR 100,000 - 150,000
Yesterday
Be an early applicant

TECHNICAL ASSISTANT

Chemsain Konsultant Sdn Bhd

West Coast Division
On-site
MYR 100,000 - 150,000
Yesterday
Be an early applicant

Engineer, Manufacturing Process

Celestica Inc.

Kulim
On-site
MYR 150,000 - 200,000
Yesterday
Be an early applicant

Accounts Cum Admin (AM/ Senior Executive)

Talent Recruit

Kuala Lumpur
On-site
MYR 100,000 - 150,000
2 days ago
Be an early applicant

Engineering Manufacturing Administration

Agensi Pekerjaan Talent Focus Sdn Bhd

Seberang Perai
On-site
MYR 150,000 - 200,000
2 days ago
Be an early applicant

Quantity Surveyor

Eco World Development Group Berhad

Negeri Sembilan
On-site
MYR 40,000 - 60,000
2 days ago
Be an early applicant

Data Entry Specialist

SupportFinity™

Seremban
On-site
MYR 30,000 - 40,000
3 days ago
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Precision Data Entry & Reporting Specialist

SupportFinity™

Seremban
On-site
MYR 30,000 - 40,000
3 days ago
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PENANG, MALAYSIA – SALES & CUSTOMER SERVICE EXECUTIVE

Ferrari Expéditions SA

Penang
On-site
MYR 100,000 - 150,000
Yesterday
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Data Science Manager

NielsenIQ

Kuala Lumpur
Hybrid
MYR 60,000 - 90,000
Yesterday
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Clinical Site Associate
ICON Clinical Research
Kuala Lumpur
On-site
MYR 100,000 - 150,000
Full time
Yesterday
Be an early applicant

Job summary

A global clinical research organization is seeking a Clinical Site Associate to support the execution of clinical trials. Responsibilities include managing site communications, maintaining document accuracy, and ensuring compliance with regulations. The ideal candidate holds a Bachelor's degree and has experience in clinical research. This role offers competitive salary and diverse benefits tailored for work-life balance and well-being.

Benefits

Annual leave entitlements
Health insurance offerings
Competitive retirement planning
Employee Assistance Programme
Flexible benefits options

Qualifications

  • Minimum Bachelor's degree in a relevant field.
  • Prior experience in clinical research preferred.
  • Experience in managing documents and compliance.

Responsibilities

  • Manage site-level communications and coordinate site training.
  • Maintain Trial Master File accuracy and perform quality control.
  • Support subject tracking, data entry oversight, and system maintenance.
  • Prepare for and support audits/inspections.
  • Ensure timely data entry and support issue resolutions.

Skills

Strong organizational skills
Communication skills
Attention to detail
Ability to work independently
Ability to prioritize tasks

Education

Bachelor's degree in life sciences or healthcare
Job description
Overview

JR140855 Clinical Site Associate

ICON plc is a world-leading healthcare intelligence and clinical research organization. We’re proud to foster an inclusive environment driving innovation and excellence, and we welcome you to join us on our mission to shape the future of clinical development.

We are currently seeking a Clinical Site Associate to join our diverse and dynamic team. As an IHCRA at ICON, you will play a pivotal role in supporting the execution and management of clinical trials, contributing to the advancement of Innovative treatments and therapies.

Responsibilities
  • Site Support & Oversight: Manage site-level communications, coordinate site training and systems access, and support site readiness activities including pre/post site visit tasks, and follow-up on action items.

  • Document Management: Maintain Trial Master File (TMF) and Investigator Site File (ISF) accuracy and inspection readiness; perform quality control, filing, and tracking of essential documents in partnership with CTM, CRAs and TMF Lead as applicable.

  • Data & System Management: Support subject tracking, data entry oversight, and system maintenance in CTMS and eTMF; assist with eCRF UAT testing and clinical sample tracking.

  • Compliance & Audit Readiness: Prepare for and support audits/inspections, support CAPA implementation, and ensure adherence to protocol, GCP, and regulatory requirements.

  • Monitoring & Issue Resolution: Ensure data entry timeliness, speedy query resolution, support CRA’s with protocol deviations follow-ups, and site escalations; support SAE and external data submissions and follow up.

Your profile
  • Bachelor's degree in a relevant field, such as life sciences or healthcare

  • Previous experience in clinical research or a related field preferred

  • Strong organizational and communication skills

  • Ability to work independently and collaboratively in a fast-paced environment

  • Attention to detail and ability to prioritize tasks effectively

What ICON can offer you

Our success depends on the quality of our people. That’s why we’ve made it a priority to build a diverse culture that rewards high performance and nurtures talent.

In addition to your competitive salary, ICON offers a range of additional benefits. Our benefits are designed to be competitive within each country and are focused on well-being and work life balance opportunities for you and your family.

Our benefits examples include:

  • Various annual leave entitlements

  • A range of health insurance offerings to suit you and your family’s needs.

  • Competitive retirement planning offerings to maximize savings and plan with confidence for the years ahead.

  • Global Employee Assistance Programme, LifeWorks, offering 24-hour access to a global network of over 80,000 independent specialized professionals who are there to support you and your family’s well-being.

  • Life assurance

  • Flexible country-specific optional benefits, including childcare vouchers, bike purchase schemes, discounted gym memberships, subsidized travel passes, health assessments, among others.

At ICON, inclusion & belonging are fundamental to our culture and values. We’re dedicated to providing an inclusive and accessible environment for all candidates. ICON is committed to providing a workplace free of discrimination and harassment. All qualified applicants will receive equal consideration for employment without regard to race, color, religion, sex, sexual orientation, gender identity, national origin, disability or protected veteran status.

If, because of a medical condition or disability, you need a reasonable accommodation for any part of the application process, or in order to perform the essential functions of a position, please let us know or submit a request here. (Reasonable accommodations process information removed)

Interested in the role, but unsure if you meet all of the requirements? We would encourage you to apply regardless – there’s every chance you’re exactly what we’re looking for here at ICON whether it is for this or other roles.

Are you a current ICON Employee? Please apply through the official channels.

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* The salary benchmark is based on the target salaries of market leaders in their relevant sectors. It is intended to serve as a guide to help Premium Members assess open positions and to help in salary negotiations. The salary benchmark is not provided directly by the company, which could be significantly higher or lower.

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