JUMP TO CONTENT

Medical Project Specialist (Real world CRA)

  1. Hong Kong
2024-112604
  1. Clinical Monitoring
  2. ICON Strategic Solutions
  3. Office Based

About the role

This vacancy has now expired. Please click here to view live vacancies.

As a Medical Project Specialist you will be joining the world’s largest & most comprehensive clinical research organisation, powered by healthcare intelligence.

Working Location: Hong Kong client office based


What you will be doing:

  • Design and/or implement a series of local/regional/global planned LDGs, HECON and Post Approval Studies/researches with customers:
    • Work closely with internal and external stakeholders to implement and track the studies timely with quality, within budget and compliant.
    • Plan and evaluate study timeline, fair market value, budget and all resource required
    • Communicate with study related team regarding budget allocation and executive plan.
    • Generate site feasibility questionnaire and conduct site feasibility visit to enroll qualified sites
    • Generate start-up plan to ensure study can be initiated according to planned timeline
    • Prepare IRB and RA submission dossier
    • Arrange study material allocation and delivery
  • Design and/or implement a series of local/regional/global planned Investigator studies and in scope research types with customers:
    • Conduct denied paries screening and anti-bribery/corruption checks
    • Ensure Fair Market Value assessment is completed as appropriate
    • Negotiate contracts and budget with investigators and hospitals
    • Send quarterly status update report request
    • Ensure study database is updated and maintained throughout the study phase
    • Provide professional guidance to investigators
  • Maintain good relationship with site personnel
  • Involve and/or conduct audit, inspections and other quality assurance activities
  • Contribute to Medical Scientific Affairs operational excellence

You are:

  • Bachelor's degree in life science courses (Pharma, Biology, Medical Science, Nursing, etc)
  • At least 1-3 years of handling experience in clinical trials or investigator-initiated studies
  • Strong project management skills and sense of urgency
  • Clinical study execution related knowledge, including but not limited to GCP, GPP, IRB submission, etc.
  • Demonstrate ethics and integrity
  • Driven result, focus on customers and patients
  • Proficiency in Cantonese and English


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 maximise savings and plan with confidence for the years ahead
  • Global Employee Assistance Programme, TELUS Health, offering 24-hour access to a global network of over 80,000 independent specialised 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, subsidised travel passes, health assessments, among others



Visit our careers website to read more about the benefits of working at ICON: https://careers.iconplc.com/benefits

At ICON, diversity, inclusion & belonging are fundamental to our culture and values. Our rich diversity makes us more innovative which helps us better serve our people, patients, customers, and our communities. We're proud of our diverse workforce and the work we’ve done to become a more inclusive organisation. 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 through the form below.

https://careers.iconplc.com/reasonable-accommodations

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.

 

#LI-ST1

#LI-Hybrid

List #1

Day in the life

A picture of chemists on a superimposed periodic table
5 reasons why you should consider a career in Clinical Research

Teaser label

Inside ICON

Content type

Blogs

Publish date

01/17/2025

Summary

Five Reasons Why You Should Work at a Contract Research Organization Contract research organisations (CROs) play a pivotal role in advancing medical science, offering career opportunities that are

Teaser label

If you’re seeking a rewarding and fulfilling work environment, a career at a CRO might be the perfect fit.

Read more
Man with headphones on looking at a laptop
Tips to make a lasting impression in a video interview

Teaser label

Career Progression

Content type

Blogs

Publish date

05/10/2024

Summary

Although many employers are returning to the office, we’re still seeing a mix of both video and in-person interviews in application processes. Early in 2020, the number of companies using video interv

Teaser label

Ace your virtual job interview with these proven video interview tips.

Read more
A picture of Debora Oh
How to excel as a CRA in a Clinical Research Organisation

Teaser label

Our People

Content type

Blogs

Publish date

08/29/2023

Summary

To excel as a Clinical Research Associate (CRA) in a Clinical Research Organization (CRO), you need a combination of education, skills, and the right mindset. Brazil-based CRA II Debora shares her

Teaser label

Brazil-based CRA II Debora Oh shares her tips on how to become a great CRA and provides insight into life at ICON.

Read more
View all

Similar jobs at ICON

Senior Clinical Research Associate - Quebec

Salary

Location

Canada

Department

Clinical Monitoring

Location

Canada

Remote Working

Remote

Business Area

ICON Strategic Solutions

Job Categories

Clinical Monitoring

Job Type

Permanent

Description

As a CRA you will be joining the world’s largest & most comprehensive clinical research organization, powered by healthcare intelligence. En tant qu’ARC (Associé(e) de recherche clinique), vous rejoin

Reference

2025-121578

Expiry date

01/01/0001

Jamie Pruitt

Author

Jamie Pruitt
Read more Shortlist Save this role
CRA II

Salary

Location

UK, Reading

Department

Clinical Monitoring

Real World Solutions

Location

Reading

Remote Working

Office or Home

Business Area

ICON Full Service & Corporate Support

Job Categories

Clinical Monitoring

Job Type

Permanent

Description

We are currently seeking a Clinical Research Associate II for our full service team in the UK. As a Clinical Research Associate II at ICON, you will play a pivotal role in designing and analyzing clin

Reference

JR136463

Expiry date

01/01/0001

Sophie Bingham Read more Shortlist Save this role
Senior Clinical Research Associate - southern Germany

Salary

Location

Germany

Department

Clinical Monitoring

Location

Germany

Remote Working

Remote

Business Area

ICON Strategic Solutions

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

2025-121769

Expiry date

01/01/0001

Roxana Rosca

Author

Roxana Rosca
Read more Shortlist Save this role
Clinical Research Associate - 12 months' monitoring experience required

Salary

Location

UK, Reading

Location

Reading

Remote Working

Office or Home

Business Area

ICON Strategic Solutions

Job Categories

Clinical Monitoring

Job Type

Permanent

Description

Role: Clinical Research Associate (12+ months' monitoring experience required) Location: Must be based in the UK, ideally in the Midlands or south West of the UK (nationwide travel) Fully sponsor dedi

Reference

JR136398

Expiry date

01/01/0001

Amani Yousef

Author

Amani Yousef
Read more Shortlist Save this role
CRA II

Salary

Location

Netherlands

Department

Clinical Monitoring

Location

Netherlands

Remote Working

Remote

Business Area

ICON Strategic Solutions

Job Categories

Clinical Monitoring

Job Type

Permanent

Description

As a Clinical Research Associate (CRA) you will be joining the world’s largest & most comprehensive clinical research organisation, powered by healthcare intelligence. For one of our sponsors, (based

Reference

2025-121531

Expiry date

01/01/0001

Iris Brouwer

Author

Iris Brouwer
Read more Shortlist Save this role
Sr. Clinical Research Associate

Salary

Location

Croatia, Zagreb

Location

Zagreb

Remote Working

Remote

Business Area

ICON Strategic Solutions

Job Categories

Clinical Monitoring

Job Type

Permanent

Description

We are looking to recruit experienced Senior CRA to join our ICON FSP team and work in a sponsor dedicated role for a global biopharmaceutical company who are the leader in fastest growing modern heal

Reference

JR135821

Expiry date

01/01/0001

Dariusz Sternlicht Read more Shortlist Save this role
View Jobs

Browse popular job categories below or search all jobs above