What Jobs are available for Research Coordinator in Hong Kong?

Senior Manager (at the rank of Administrative Assistant II), HKU Jockey Club Enterprise Sustainability Global Research Institute in the Faculty of Business and Economics (Ref.: to commence as soon as possible, on a two-year fixed-term basis, with contract-end gratuity and University contribution to a retirement benefits scheme, totaling up to 10% of basic salary, with the possibility of renewal subject to satisfactory performance)

The HKU Jockey Club Enterprise Sustainability Global Research Institute is a strategic collaboration between The University of Hong Kong (HKU) and The Hong Kong Jockey Club (HKJC). Its goal is to create a world-class hub and network of distinguished scholars in Governance and Sustainability worldwide. To achieve this, the Institute offers various forms of support, including grants and publicity, to its affiliated scholars.

Applicants should possess a bachelor's degree or above in business-related disciplines with a minimum of 6 years' relevant administrative, project management, and/or communications experience, including at least 3 years' work experience at supervisory role. Experience working in international environment and/or interacting with academic researchers are highly advantageous.

They should have demonstrated success in orchestrating communications and efforts towards an organization's strategic goals, managing projects in compliance with guidelines and processes of public organisations, managing stakeholders from various teams and departments. They should also have excellent verbal and written communication skills, in both Chinese and English. They should show proven ability to communicate confidently with staff at all levels and establish networks within the HKU Business School overseas and in China.

The appointee will have the primary job responsibilities include, but not limited to, the following:

• Curate and maintain a strong network of HKU and global scholars affiliated with the Institute, with communications/publicity, events, and resource support listed below

• Coordinate communications effort in various digital channels (social media, eDM) to promote the Institute and the Faculty internationally, including but not limited to research spotlight and event recap

• Manage and organize the Institute's research events

• Manage the Institute's research budget, including the operation and management of any relevant grant, prize and sponsorship schemes, in compliance with relevant guidelines from the Faculty

• Manage and organize the Institute's research support initiatives, including but not limited to a potential data platform and data acquisitions, and publications to promote research work by the Institute's affiliates

• Perform any other duties as assigned by supervisors

• Work outside normal office hours may be required.

A highly competitive salary commensurate with qualifications and experience will be offered, in addition to annual leave and medical benefits.

The University only accepts online applications for the above post.  Applicants should apply online at the University's careers site ) and upload an up-to-date C.V.  Review of applications will commence as soon as possible and continue until August 17, 2025, or until the post is filled, whichever is earlier.

The University is an equal opportunities employer and

is committed to equality, ethics, inclusivity, diversity and transparency

Job Title:Assistant Librarian/Assistant Manager (Research & Learning Support)

Department:Library

Job ID:10882

Job Posting Details

As a key member of HKUST Library's Research & Learning Support team, dedicated to enhancing information literacy, research workflows, and academic success for students and researchers through innovative library services, the appointee will assist in:

• Designing, developing, and delivering engaging information and digital literacy learning programs face to face or online.

• Create appealing content for learning and community outreach, including videos, interactive games, quizzes, and posters.

• Collect and analyze library data, including learning assessments, to support evidence-based decision-making.

• Contribute to the organization and management of scholarly outputs and other research support services.

• RLS unit administration, including office management, library classes, information services, student helper supervision, and outreach activities.

Required Qualifications

Applicants must have:

• A bachelor's degree with at least 3 years' relevant work experience.

• Strong motivation, proactivity, and the ability to multitask effectively in a fast-paced, collaborative environment.

• Excellent written and spoken English; proficiency in Chinese (Cantonese and Putonghua) is an advantage.

Desirable Qualifications

• A Master's degree in Library Science (MLS) or equivalent.

• Academic background or experience in creative media, or data analysis and visualization will be an advantage

• Proficiency in graphic design tools (e.g., Adobe Creative Cloud, Canva) and/or programming languages (e.g., Python) is highly desirable.

• A portfolio showcasing visuals, e-learning content, or related work is strongly preferred.

Candidates with a keen interest in information literacy, visual learning, information visualization, or research management and less experience are encouraged to apply and will be considered. (Duration: 2 years, renewable).

(Applicants who have responded to the previous advertisements need not re-apply.)

Starting salary will be commensurate with qualifications and experience.  Fringe benefits including annual leave, medical and dental benefits will be provided.  A gratuity will be payable upon successful completion of contract.

Application Procedure

In support of a green work environment, we accept applications submitted online only.  To apply, please complete an online application form through the HKUST Careers website ) and return it online to the Human Resources Office on or before Monday, 29 September Applicants will receive an acknowledgement by email upon successful submission.  We thank applicants for their interest, but advise that only shortlisted candidates will be notified of the result of the application.

(Information provided by applicants will be used for recruitment and other employment-related purposes.  Applicants should read the Personal Information Collection Statement before submission of application.)

HKUST is an equal opportunities employer and is committed to our core values of

inclusiveness, diversity, and respect.

Qube Research & Technologies (QRT) is a global quantitative and systematic investment manager, operating in all liquid asset classes across the world. We are a technology and data driven group implementing a scientific approach to investing. Combining data, research, technology, and trading expertise has shaped our collaborative mindset, which enables us to solve the most complex challenges. QRT's culture of innovation continuously drives our ambition to deliver high quality returns for our investors.

Your future role within QRT

You will join the Research & Trading Data production support team which is a part of the larger Production Management team in Hong Kong, providing production and research data support to QRT's trading and research teams. In this role, you will be responsible for delivering prompt user support, investigating and resolving issues affecting production and research data, onboarding data extraction processes, and liaising with internal and external teams to ensure the effective day-to-day management of QRT's data infrastructur

**e.

What you will**

• do

Provide support for QRT's data system infrastructure, including extractors, pipelines, and data operations across research and tra
- dingUse cloud platforms to create and monitor data jobs and proce
- ssesSupport data systems and tasks running on Windows & Linux environm
- entsEnsure production and research data systems are stable and available, with all critical data tasks completed before the start of each trading
- dayCollaborate with production support teams and developers to investigate and resolve issues qui
- cklySupport the release management process ensuring stability of the production environ
- mentMaintenance and support of static databases and supporting proce
- ssesDevelop monitoring tools to improve visibility, reliability, and automation of proces
- ses.Evening/weekend support requirements (normally, through remote acc

**ess)

Requirem**

• ents

Minimum 3 years in a suppor
- t role2+ years of experience with Bash, PowerShell, Git, Python scr
- iptingBasic understanding of cloud se
- rvicesExcellent problem solving and highly effective analytics capabilities re
- quiredMust have a keen focus on ownership of issues and commitment to resolvin
- g themExcellent written and oral communication skills are ess
- entialExpert windows desktop and server administration experience is ess
- entialHigh level of Linux OS experience is ess
- entialExpert relational database skills (in order of preference: SQL Server, Postgres) are ess

**ential

Good-t**

• o-have

Experience managing the expectations of Front Office traders and senior ma
- nagementKnowledge of Equities, Futures, Commodities and FX asset
- classesKnowledge of market data feed handlers and executi
- on feedsKnowledge of market-making/liquidity provision and algorithmic

trading

QRT is an equal opportunity employer. We welcome diversity as essential to our success. QRT empowers employees to work openly and respectfully to achieve collective success. In addition to professional achievement, we are offering initiatives and programs to enable employees achieve a healthy work-life

balance.

Join our client's team and put your bilingual Chinese-English skills to work They are seeking detail-oriented professionals with strong data entry and spreadsheet experience. If you have an Android phone, a reliable computer with internet access, and the ability to follow clear instructions with precision, this opportunity is for you. Bring your accuracy, focus, and dedication to a role where your skills make a real impact. Apply today to take the next step in your career

Job Highlights

• Hourly Rate
  : USD 5, the equivalent in your local currency
• Paid Hours per Week:
  40 Hours
• Schedule:
  Monday – Friday, 9:00 AM – 6:00 PM Pacific (includes 1-hour unpaid break) |
  Client Timezone:
  Pacific Time
• Work Arrangement:
  Work from home
• Contract:
  Independent Contractor

Side note:
Since this is a permanent work-from-home position and an "Independent Contractor" arrangement, the candidates must have their own computer and internet connection. They will handle their own benefits and taxes. The professional fees are on hourly rates and the rate depends on your performance in the application process.

Scope

• 6-month project (ongoing until March 2026)
• Remote work with direct client management
• Work as part of a 4–5 person team collecting ~20,000 data points

Responsibilities

• Navigate Chinese-language mobile apps (Meituan and Alibaba's Ulema)
• Collect and extract specific data points from food delivery platforms
• Enter collected data into structured spreadsheets
• Follow established data collection processes and procedures
• Report daily progress to client management
• Ensure accuracy and consistency across all data entry tasks

Requirements

• Fluent in Chinese and English (bilingual capability essential)
• Own an Android phone for platform access
• Reliable computer/laptop with internet connection
• Experience with basic data entry and spreadsheet software
• Strong attention to detail and ability to follow instructions precisely

Independent Contractor Perks

• HMO coverage (eligible locations)
• Permanent work from home
• Immediate hiring

Reminder:

Kindly apply directly to the
link
provided; you will be redirected to BruntWork's Career Site. Complete the initial requirements, including the voice recording, pre-screening assessment, and technical check of your computer/device.

ZR_28099_JOB

This role is for upcoming future opportunities that may arise at Fortrea.

Fortrea is excited to connect with talented individuals for future opportunities. If you meet the job requirements, we'll invite you for an interview. If you're pre-selected, our recruiter will keep in touch and let you know when the role officially opens, so we can reconfirm your interest before moving forward with an offer.

Summary of Responsibilities:

• Site management responsibility for clinical studies according to Fortrea's Standard Operating Procedures, ICH GCP Guidelines, applicable project plans and Sponsor requirements, including verification of study training records.
• Conducts site monitoring responsibilities for clinical trials according to Fortrea's Standard Operating Procedures (SOPs), ICH guidelines and GCP; including Pre-study, Site Initiation, Process Monitoring, Routine Monitoring, and Close-out Visits.
• Prepares and implements project plans related to Clinical Monitoring responsibilities.
• Ensures the protection of subjects by verifying that informed consent procedures and protocol requirements are adhered to alongside applicable regulatory requirements.
• Safeguards data integrity by careful source document review, source document verification, query generation, and resolution against established data review guidelines on Fortrea or client data management systems.
• Confirms Site Regulatory documents and applicable eTMF/Sponsor Documents are complete and current throughout the duration of the trial.
• Guarantees that the study Investigational Product inventory and accountability is accurate and that study materials are stored securely and per protocol requirements.
• Ensures adherence to global quality control and CRA performance metrics.
• Ensures audit readiness at site level.
• Acts in the project role of a Lead CRA as assigned.
• General On-Site Monitoring Responsibilities:
• Ensure the study staff who will conduct the protocol have received the proper materials and instructions to safely enter subjects/patients into the study. Ensure the protection of study subjects or patients by performing eligibility review, verifying that screening, informed consent procedures and protocol requirements are adhered to according to the applicable regulatory requirements.
• Ensure the integrity of the source data reported by careful source document review. Monitor data for missing or implausible data.
• Ensure study data completeness, accuracy, consistency, and compliance; identify deficiencies, deviations and discrepancies, and initiate corrective action as required.
• Ensure the resources of the Sponsor and Fortrea are spent wisely by performing the required monitoring tasks in an efficient manner, according to SOPs and established guidelines, including managing travel expenses in an economical fashion according to Fortrea travel policy.
• Travel, including air travel, may be required and is an essential function of the job.
• Prepare and submit accurate and timely trip reports.
• Independently perform eCRF review, 100% source data verification, query generation and resolution against established data review guideline with or without direct supervision, on Fortrea or client data management systems, as assigned by management.
• Assist with the administration of clinical research projects, recruiting investigators (if applicable), collecting investigator documentation and site management.
• Update, navigate, and maintain Fortrea or study/Sponsor-specific trial management tools/eClinical systems.
• Track IP shipments and supplies, as needed.
• Track and follow-up on serious adverse events as assigned.
• Work closely with the study team, align monitoring to critical study timelines ensuring study deliverables are met.
• Prepare and implement study-specific monitoring plans and site Initiation slides, as assigned.
• Attend investigators' meetings (if applicable), project team meetings and teleconferences, and others as needed.
• Present training content for site initiation.
• Assist with training of new employees (e.g., co-monitoring).
• All other duties as needed or assigned.

Qualifications (Minimum Required):

•B.A./B.S. (Life Science preferred) or equivalent healthcare experience.

•Minimum 1 year experience as CRA. Has conducted on site monitoring in Hong Kong in the past 3 months.

•In lieu of the above requirement,

-CRA II: candidates with 2 more years of CRA monitoring experience in pharmaceutical or CRO industries may be considered.

-SCRA: candidates with 3 more years of CRA monitoring experience in pharmaceutical or CRO industries may be considered.

•Basic understanding of ICH Guidelines and GCP including a basic understanding of regulatory requirements.

•Basic understanding of the clinical trial process.

•Fluent in local language and English.

Fortrea is actively seeking motivated problem-solvers and creative thinkers who share our passion for overcoming barriers in clinical trials. Our unwavering commitment is to revolutionize the development process, ensuring the swift delivery of life-changing ideas and therapies to patients in need. Join our exceptional team and embrace a collaborative workspace where personal growth is nurtured, enabling you to make a meaningful global impact. For more information about Fortrea, visit

Clinical Research Associate (at the rank of Technical Officer/Research Assistant I/II) in the Clinical Trials Centre (Ref:

The Clinical Trials Centre (HKU-CTC) is a leading clinical trials management platform established under The University of Hong Kong LKS Faculty of Medicine (HKUMed) and is dedicated to managing and facilitating international-standard clinical trials on new drugs, medical devices and medical technologies.  HKU-CTC offers long-term development opportunities to passionate talents who are devoted to a career in the clinical trial profession.

Clinical studies are highly sophisticated, multi-disciplinary projects that require good planning, close monitoring and synchronization of research team members and activities.  HKU-CTC's Project Operations Unit (POU) is a professional unit dedicated to facilitating clinical study planning, performance and completion in compliance with international standards and in an efficient and high-quality manner.  POU is seeking talents who are interested/experienced in practising the project management profession in clinical research.  Comprehensive on-job training will be provided.  Fresh graduates will also be considered.

Main Responsibilities:

• Act as a key contact person among clinical study centres, sponsoring companies, regulatory authorities and other stakeholders to coordinate clinical trial activities;
• Facilitate the planning, initiation and monitoring of clinical studies throughout their project life cycles, ensuring adherence to protocols and regulatory requirements;
• Assess the feasibility of clinical studies at potential sites to support study planning;
• Conduct various visits (including Pre-Study Visits (PSV), Site Initiation Visits (SIV), Site Closure Visits (COV) and Monitoring Visits (MV)) to verify compliance, data integrity, and participant safety;
• Support study planning, preparation and initiation (e.g. setting study time plans/milestones, assisting in obtaining ethics and regulatory approvals, importing study products, coordinating logistics and workflows, and organizing study setup);
• Review and verify study data and source documentation for accuracy and completeness;
• Monitor the progress and quality of study activities (both on-site at study centres and remotely via electronic data capture systems);
• Oversee study centres' compliance with study protocols, Good Clinical Practice (GCP) and other research ethics and regulatory requirements, prepare and write monitoring reports;
• Assist in the proper closure of clinical studies;
• Facilitate study audits and inspections as needed; and
• Perform other duties related to clinical trial management as assigned.

Requirements:

• Bachelor's degree or above in Health, Biological/Life Sciences, Medical, Pharmacy, Nursing or related disciplines;
• Experience in clinical research operations and development, and/or basic knowledge in Good Clinical Practice (GCP) are added advantages;
• Good interpersonal and communication skills allowing collaboration with cross-functional teams;
• Good coordination and problem-solving skills, and commitment to quality and compliance;
• Detail-minded, able to handle multiple concurrent tasks, and have a strong sense of responsibility; and
• Good command of written and spoken English and Cantonese (proficiency in Putonghua is a plus).

The appointment will commence as soon as possible on a 1-year temporary basis or 2-year fixed-term basis, with the possibility of renewal subject to satisfactory performance.  A highly competitive salary commensurate with qualifications and experience will be offered, in addition to annual leave and medical benefits.  Appointment on 2-year fixed term basis will attract a contract-end gratuity and University contribution to a retirement benefits scheme, totalling up to 10% of basic salary.

Application Procedure

The University only accepts online application for the above post.  Applicants should apply online at the University's careers site ) and upload an up-to-date C.V.  Review of applications will start from October 9, 2025 and continue until October 25, 2025, or until the post is filled, whichever is earlier.

CRA II/ Senior CRA - office-based in Hong Kong. Join us and advance your career with an industry leading CRO.

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 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 trial activities to ensure they are conducted according to protocol, regulatory requirements, and industry standards. You will contribute to the success of clinical trials by ensuring data integrity, participant safety, and compliance throughout the study lifecycle.

What You Will Be Doing

• Monitoring clinical trial sites to ensure adherence to study protocols, regulatory requirements, and Good Clinical Practice (GCP) standards.
• Conducting site visits to assess site performance, resolve issues, and provide support to ensure successful trial execution.
• Collaborating with cross-functional teams to ensure timely and accurate data collection and reporting.
• Providing training and guidance to site staff and other CRAs to maintain high standards of clinical trial conduct.
• Building and maintaining effective relationships with site personnel and stakeholders to facilitate smooth trial operations.

Your Profile

• Advanced degree in a relevant field such as life sciences, nursing, or medicine.
• Extensive experience as a Clinical Research Associate, with a strong understanding of clinical trial processes and regulatory requirements.
• Proven ability to manage multiple sites and projects simultaneously, with strong organizational and problem-solving skills.
• Expertise in monitoring practices, data integrity, and site management, with proficiency in relevant clinical trial software and tools.
• Excellent communication, interpersonal, and stakeholder management skills, with the ability to influence and drive compliance within a complex environment.
• Ability to travel at least 60% of the time (international and domestic - fly and drive) and should possess a valid driver's license

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