Senior CRA

Senior CRA

Location

Kuala Lumpur

Reference: JR159500

Categories Clinical Monitoring

-vacancyopjusttionswidget.opt-Business Area ICON Full Service & Corporate Support

-__vacancyopjusttionswidget.opt-Remote Working __ Remote or Office

About the role

Clinical Research Associate I/II

ICON is a global healthcare intelligence and clinical research organisation united by a mission to bring new medicines and treatments to patients faster.

As a values-driven organisation, integrity, collaboration, agility, and inclusion are at the heart of how we work and interact with each other, customers, patients and suppliers.

Work location: Home-based in Bangkok, Thailand

As a CRA II at ICON, you will design and analyse clinical trials, interpreting complex medical data, and contribute to the advancement of innovative treatments and therapies.

What You Will Do:

You will contribute to clinical trial monitoring activities, taking responsibility for your deliverables and working collaboratively.

Key responsibilities include:

• Conducting site qualification, initiation, monitoring, and close-out visits for clinical trials.
• Ensuring protocol compliance, data integrity, and patient safety throughout the trial process.
• Collaborating with investigators and site staff to facilitate smooth study conduct.
• Performing data review and resolution of queries to maintain high-quality clinical data.
• Contributing to the preparation and review of study documentation, including protocols and clinical study reports

Your Profile:

You will bring relevant clinical trial monitoring experience, along with the following qualifications and skills.

Required qualifications and experience:

• Bachelor's degree in a scientific or healthcare-related field.
• 2+ years of Global SIT Phase I to III onsite monitoring CRA experience: Oncology, Endocrinology or Cardiology is mandatory.
• In-depth knowledge of clinical trial processes, regulations, and ICH-GCP guidelines.
• Strong organizational and communication skills, with attention to detail.
• Ability to work independently and collaboratively in a fast-paced environment.
• Willingness to travel as required

LI-DP1

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.

Visit our careers site to read more about the benefits ICON offers.

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

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 click here to apply

Share:

Location

Kuala Lumpur

Reference: JR159500

Categories Clinical Monitoring

-vacancyopjusttionswidget.opt-Business Area ICON Full Service & Corporate Support

-__vacancyopjusttionswidget.opt-Remote Working __ Remote or Office

Not Ready to Apply?

Join our Talent Community for future alerts.

Sign up

Explore more about ICON

About ICON

Explore

Global Office Locator

Explore

Benefits & Rewards

Explore

Inclusion & Belonging

Explore

Career Pathways

Explore

Environmental, Social & Governance

Explore

List #1

Day in the life

Suzaita's story - an insight into working in Clinical Research

Teaser label

A Day In The Life

Content type

Blogs

Publish date

04/05/2023

Summary

Senior Clinical Research Associate Suzaita Hipolito talks about the satisfaction gained from working in Clinical Research. “What would it look like to wake up every day feeling happy and fulfil

Teaser label

Senior Clinical Research Associate, Suzaita Hipolito, talks about how working in Clinical Research gives her happiness and fulfilment.

Read more

by

Suzaita Hipolito

by

Suzaita Hipolito

View all

Similar jobs at ICON

Clinical Site Associate

Location

Spain, Madrid

Department

Clinical Monitoring

Location

Barcelona

Madrid

Remote Working

Hybrid

Business Area

ICON Full Service & Corporate Support

Job Categories Clinical Monitoring

Job Type Permanent

Description

• As a Clinical Site Associate at ICON, you will support site management activities and ensure that clinical trials are conducted efficiently, compliantly, and to the highest quality standards.

• What You

• Reference

• JR159616

• Expiry date

• 01/01/0001

• Author

• Lourdes Roy Prats

• Author

• Lourdes Roy Prats

• Read more

• Shortlist Save this role

• Read more

• Shortlist Save this role

• Clinical Research Associate 1

Location

Spain, Barcelona

Remote Working

Remote or Office

Business Area

ICON Strategic Solutions (FSP)

Job Categories Clinical Monitoring

Job Type Permanent

Description

• As a CRA I at ICON, you will contribute to our clinical trial operations function, working collaboratively to deliver high-quality outcomes across our clinical programmes. What You Will Do:Your role w