What Jobs are available for Research Study in Hong Kong?

招聘職位 Job Title

中國科學院香港創新研究院科技處項目管理

Coordinator, Scientific and Technological Department, Hong Kong institute of Science & Innovation, Chinese Academy of Sciences

工作地址 Office Address

中國香港特別行政區新界沙田白石角香港科學園10W 7層

7/F, Building 10W (Lakeside 2), Hong Kong Science Park West Avenue 10, Sha Tin

工作職責 Responsibilities

1.負責聯繫國家科技部、國家自然科學基金委、香港創新科技署等內地及香港相關科技管理部門,組織科研項目申報工作;

Liaise with relevant technology management authorities in mainland China and Hong Kong, including the Ministry of Science and Technology, the National Natural Science Foundation of China, and the Hong Kong Innovation and Technology Commission, and organize research project applications.

2.負責聯繫中國科學院各院屬單位,科研項目策劃、組織申報和管理工作;

Coordinate with the institutions under the Chinese Academy of Sciences to plan, apply for, and manage projects.

3.承擔重大科技活動和學術活動的組織協調;

Organize and coordinate major scientific and academic events.

4.負責知識產權和成果轉化管理工作;

Manage intellectual property and technology transfer on a daily basis.

5.負責對外科技合作和課題管理工作;

Oversee international scientific cooperation and research project management.

6.負責領導交辦的其他工作。

Perform other duties as assigned by leadership.

應聘條件 Requirements

1.具有良好道德品質及職業操守,愛國愛港,遵紀守法;

Demonstrates excellent moral character and professional ethics; patriotic, committed to Hong Kong SAR, and compliant with laws and regulations.

2.碩士研究生學歷並具有3年及以上相關工作經驗,過往業績良好,或具有博士研究生學歷;

Holds a master's degree with generally 3 or more years of relevant work experience and a proven track record of performance, or a doctoral degree.

3.具有較高的職業素質,較強的責任心,服務意識及溝通協調能力;

Possesses strong professional qualities, a high sense of responsibility, service orientation, and excellent communication and coordination skills.

4.具有良好的普通話、英語、粵語書寫和表達能力。

Proficient in written and spoken Mandarin, English, and Cantonese.

5.信息技術或生命科技專業領域優先。

Priority given to candidates with academic backgrounds in information technology or life sciences.

應聘事項 Remarks

薪酬福利綜合確定,以最終簽訂的僱傭合約為準。

Remuneration package shall be reviewed with consideration, and subject to the Employment Contract.

自發佈招聘啟事起,凡符合應聘條件的人員均可報名。

Since release of the job ads, all interested applicants are welcomed to apply.

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

Established by Tung Wah Group of Hospitals ("TWGHs") in 2010, Tung Wah College (TWC) is a self-financing degree-granting institution registered under the Post Secondary Colleges Ordinance (Cap Following the educational ideals of TWGHs and leveraging on its renowned strengths and expertise, TWC aims to provide high quality tertiary education to nurture competent, socially responsible and caring professionals for the benefits of society.

With the staunch support of TWGHs, TWC has been developing rapidly and built up a niche in healthcare education. It is the first self-financing tertiary institution offering five professionally accredited degrees to train nurses and allied health professionals such as medical laboratory technologists, occupational therapists and radiation therapists. Besides, the College is also the first institution registered under Cap. 320 offering early childhood education degree and higher diploma programmes to train qualified kindergarten teachers and childcare professionals.

Currently, TWC has 4 schools (namely School of Arts and Humanities, School of Management, School of Medical and Health Sciences, and School of Nursing) running a total of 19 degree, sub-degree and diploma programmes in several disciplines.  It has a student population of over 4,000 in 2024/2025.

Being a young and vibrant institution, TWC aspires to become a leading private university in the long term.  It is planning to launch a number of new programmes, strengthen teaching and learning facilities and quality, and enhance research capability etc. in coming years.  To cope with its continuous development, we are now inviting highly qualified candidates to fill the following post:

Research Nurse/ Clinical Research Associate,

School of Nursing

(TWC/25/172/NUR/RN_CRA)

Duties

The appointee will provide support to the project "Diagnosis accuracy of a combination of near-infrared spectroscopy (fNIRS) and plasma biomarkers". Duties will be required but not limited to:

•    reviewing literature; providing administrative support;

•    ethical application;

•    collecting and analyzing quantitative data;

•    assisting the research team in preparing research reports;

•    conducting data analysis using SPSS, NVivo, or other tools such as Python and R; and

•    performing other tasks and duties as assigned to support the operation of the project.

Requirements

Applicants should:

•    hold a valid license as a Registered Nurse (RN) or Enrolled Nurse (EN) in his/her own region;

•    possess the skill of blood taking;

•    possess a bachelor's degree or above in Nursing (preferably Master);

•    have at least two years of clinical and research experience;

•    good interpersonal skills, and a strong sense of responsibility;

•    the ability to multitask independently; and

•    proficiency in both written and spoken Chinese (Cantonese) and English.

Applicants with less experience will be considered.

Salary will be competitive and commensurate with qualifications and experience.

To apply, please submit your application letter, resume and a completed application form (available at ) by mail to the Human Resources Office, Tung Wah College Cheung Kung Hai Memorial Building, 90A Shantung Street, Mongkok, Kowloon or email to   Please quote the reference number of the post in the application letter and on the envelope.  The College reserves the right to fill or not to fill the post.  Applicants who are not contacted by the College 6 months after the application deadline may consider their applications unsuccessful. For enquiries, please phone or send WhatsApp to

Application Deadline: 10 October 2025 (Friday)

All information and personal data collected will be used solely for recruitment related purposes. For more information about the College, please visit our website:

WE ARE AN EQUAL OPPORTUNITIES EMPLOYER

Are you interested in joining a team of systemic thinkers and practitioners in Asia in developing family therapy? We are looking for staff who share our values and perspectives. Come join our team where you can make a difference

Qualifications and Duty Requirements include:

·    At least Bachelor Degree holder from a recognized institution

·    Proficiency in Microsoft Office programs

·    Good command of written and spoken English and Chinese

·    Must be organized and able to handle a large volume of clinical data

·    Must be able to maintain good relationship with community stakeholders and the administrative/ research team

·    Ability to work a flexible schedule including both days and nights performing research or data entry, may require to work on weekday evenings and on Saturdays

·    Duties include assisting with academic and clinical research activities including literature reviews, data collection and data analysis as well as administrative duties such as organizing meetings, preparing program reports and meeting minutes

·    Performs other duties as assigned by supervising instructor

·    Salary negotiable

Interested parties, please send your cover letter, full resume with current & expected salary, and availability to us.

Job Posting Details

Key Responsibilities:

• Assist in research on visual and multimodal algorithms, including Visual Language Models (VLM), OCR, object detection/segmentation/recognition, image/video generation, and authenticity verification, particularly for financial and related applications.
• Support research on time series and spatio-temporal data analysis, including modeling, prediction, anomaly detection, and multimodal fusion with visual/language data.
• Keep up-to-date with state-of-the-art algorithms in image, video, multimodal, time series, and spatio-temporal domains; help design and implement algorithm pipelines under the guidance of senior researchers.
• Support data collection, preprocessing, cleaning, and quality assurance to ensure datasets (including sequential and spatio-temporal data) are ready for model training and evaluation.
• Implement and fine-tune machine learning and deep learning models using frameworks such as PyTorch and TensorFlow; assist in analyzing and optimizing model performance through experiments.
• Participate in technical seminars and group discussions, learning advanced algorithms and applying them to practical research projects.
• Contribute to research under supervision in academic conferences and journals.

Requirements:

• Bachelor's or Master's degree in Computer Science, Artificial Intelligence, Machine Learning, Electronic Engineering, Information Engineering, Mathematics, or a related field, with some research or project experience.
• Passion for data-oriented work with basic experience in data analysis, cleaning, or engineering; strong programming skills are required.
• Familiarity with deep learning frameworks (PyTorch, TensorFlow), basic knowledge of time series/spatio-temporal modeling, generative algorithms, and database systems such as MongoDB is preferred.
• Publications or conference participation in AI, computer vision, multimodal learning, time series analysis, or related fields is a plus.
• Internship or project experience at technology companies is desirable.
• Interest or experience in financial technology applications, document understanding systems, or sequential data modeling (e.g., financial time series, video analysis, trajectory prediction) is a bonus.
• Ability to collaborate effectively on interdisciplinary research projects.
• Proficiency in English and Mandarin Chinese is preferred.

(Duration: 1 year, renewable)

Starting salary will be commensurate with qualifications and experience. Fringe benefits including annual leave, medical and dental benefits will be provided.

Application Procedure

Please send your application with full CV, research statement, and publication list to: Review of applications will begin immediately and continue until positions are filled. Only shortlisted candidates will be notified.

(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.