What Jobs are available for Cancer Research in Hong Kong?
Showing 39 Cancer Research jobs in Hong Kong
Clinical Research Associate
Posted today
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Job Description
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
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Clinical Research Associate
Posted today
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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.
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Clinical Research Associate II/ Senior Clinical Research Associate
Posted today
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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
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Clinical Research Associate II/ Senior Clinical Research Associate
Posted 10 days ago
Job Viewed
Job Description
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 ( 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
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(Senior) Clinical Research Associate (CRA)
Posted 14 days ago
Job Viewed
Job Description
Perform monitoring and site management work to ensure that sites are conducting the study(ies) and reporting study data as required by the study protocol, applicable regulations and guidelines, and sponsor requirements.
Essential Functions
- Perform site monitoring visits (selection, initiation, monitoring and close-out visits) in accordance with contracted scope of work and regulatory requirements, i.e., Good Clinical Practice (GCP) and International Conference on Harmonization (ICH) guidelines
- Work with sites to adapt, drive, and track subject recruitment plan in line with project needs to enhance predictability.
- Administer protocol and related study training to assigned sites and establish regular lines of communication with sites to manage ongoing project expectations and issues.
- Evaluate the quality and integrity of study site practices related to the proper conduct of the protocol and adherence to applicable regulations. Escalate quality issues as appropriate.
- Manage the progress of assigned studies by tracking regulatory submissions and approvals, recruitment and enrollment, case report form (CRF) completion and submission, and data query generation and resolution. May support start-up phase.
- Ensure copies/originals (as required) site documents are available for filing in the Trial Master File (TMF) and verify that the Investigator's Site File (ISF) is maintained in accordance with GCP and local regulatory requirements.
- Create and maintain appropriate documentation regarding site management, monitoring visit findings and action plans by submitting regular visit reports, generating follow-up letters and other required study documentation.
- Collaborate and liaise with study team members for project execution support as appropriate.
- If applicable, may be accountable for supporting development of project subject recruitment plan on a per site basis.
- If applicable, may be accountable for site financial management according to executed clinical trial agreement and retrieve invoices according to local requirement.
Qualifications
- Bachelor's Degree Degree in scientific discipline or health care preferred.
- Requires at least 1 year of on-site monitoring experience.
- Equivalent combination of education, training and experience may be accepted in lieu of degree.
- Good knowledge of, and skill in applying, applicable clinical research regulatory requirements (i.e., Good Clinical Practice (GCP) and International Conference on Harmonization (ICH) guidelines).
- Good therapeutic and protocol knowledge as provided in company training.
- Computer skills including proficiency in use of Microsoft Word, Excel and PowerPoint and use of a laptop computer and iPhone and iPad (where applicable).
- Written and verbal communication skills including good command of English language.
- Organizational and problem-solving skills.
- Effective time and financial management skills.
- Ability to establish and maintain effective working relationships with coworkers, managers, and clients.
IQVIA is a leading global provider of clinical research services, commercial insights and healthcare intelligence to the life sciences and healthcare industries. We create intelligent connections to accelerate the development and commercialization of innovative medical treatments to help improve patient outcomes and population health worldwide. Learn more at is a leading global provider of clinical research services, commercial insights and healthcare intelligence to the life sciences and healthcare industries. We create connections that accelerate the development and commercialization of innovative medical treatments. Everything we do is part of a journey to improve patient outcomes and population health worldwide.
To get there, we seek out diverse talent with curious minds and a relentless commitment to innovation and impact. No matter your role, everyone at IQVIA contributes to our shared goal of helping customers improve the lives of patients everywhere. Thank you for your interest in growing your career with us.
EEO Minorities/Females/Protected Veterans/Disabled
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Research Nurse/ Clinical Research Associate, School of Nursing
Posted today
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Job Description
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
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Research Scientist
Posted today
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Job Description
We are seeking a talented and motivated Research Scientist to join our Battery and Application Technology team. Help shape the future of battery technology by contributing to groundbreaking research and development projects.
Responsibilities
- Design and execute electrochemical tests on anode and cathode materials for aqueous battery systems.
- Develop advanced electrochemical diagnosis platforms and conduct in-situ testing on electrodes and components.
- Optimize charge-discharge and evaluation protocols to assess electrochemical performance.
- Explore and refine testing procedures for electrodes, electrolytes, and separators.
- Perform electrochemical cell teardowns and carry out failure analysis on battery materials and components.
- Visualize and analyze data, preparing comprehensive reports with actionable recommendations for battery additive R&D.
- Collaborate closely with research teams to guide promising scenarios toward production readiness.
Qualifications
- Ph.D. in Battery Chemistry, Electrochemistry, Material Chemistry, Material Physics, or a related discipline.
- 1 year of R&D experience in rechargeable battery research or energy storage materials is mandatory
- Proficiency in electrochemical testing techniques (e.g., CV, EIS, LSV, GITT), with proven ability to conduct independent R&D.
- Strong analytical and problem-solving skills, with a keen eye for data analysis and statistics.
- Excellent interpersonal and communication skills
- Strong sense of accountability, integrity, and results-oriented mindset
- Willingness to learn new concepts from patents and literature, and propose creative ideas
- Background in developing battery and inorganic materials, as well as familiarity with crystal structure analysis techniques (e.g., XRD) is preferred
- Experience with organic material development is preferred
For more company details, please visit our website at
If you are ready to drive innovation and make an impact in the world of battery technology, we would love to hear from you
We offer attractive remuneration package, 5-day work week and long-term career development opportunities to the right candidate. Please send your full resume with current and expected salary by clicking "Apply".
We are an equal opportunity employer. The information provided by you will be treated in strict confidence and used for recruitment purpose only. All personal data collected during the application process will be kept for 12 months after its completion, and will be destroyed thereafter.
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Research Scientist
Posted today
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Job Description
Are you ready to shape the future of oncology?
ZERO Biotech is a rapidly growing company at the forefront of the Nuclear Medicine revolution. As Hong Kong's pioneer in this cutting-edge field, we are developing innovative radiopharmaceuticals based on the powerful theranostic principle—to see the cancer and treat it.
We are building a world-class R&D team and will soon be joining the vibrant innovation ecosystem at the Hong Kong Science and Technology Parks (HKSTP). This is a rare opportunity to get in on the ground floor of a company with a mission to transform cancer care.
Together, we'll embark on an ambitious journey to make nuclear medicine a mainstream treatment, not just in Hong Kong but across Asia.
We are looking for passionate, high-caliber individuals to join our R&D team. If you are a visionary who thrives on challenges and wants to make a tangible impact, we want to hear from you.
Job Descriptions
· Assist in evaluating peptides or other molecules for licensing in for further drug development
· Conduct structure-activity relationship (SAR) studies to optimize compound leads
· Optimize radiolabeling methods and evaluate the properties of radiopharmaceutical candidates
· Devise and lead R&D projects best fit for company development
· Lead the application of R&D research funding application
· Lead and develop R&D team
· Stay current with state-of-the-art techniques and technologies in chemistry
Job Requirements
· Ph.D. in Chemistry, Pharmacy or other related disciplines.
· Postgraduate experience leading research projects in the capacity of Principal Investigator or in the pharmaceutical industry will be preferred
· Strong background in organic chemistry/inorganic chemistry, preferably also with background in biochemistry
· Strong knowledge of medicinal chemistry principles, drug design and optimization strategies.
· Experience working with radiopharmaceuticals is highly desirable
· Knowledge of structure-based drug design and computational chemistry tools will be advantageous.
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Research Scientist
Posted today
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Job Description
Job Description:
- Perform research directed toward investigation, evaluation, and application of known machine learning theories and principles, especially deep learning techniques.
- Plans and conducts, or direct engineering personnel performing complex engineering analyses and experiments to test, prove, or modify theoretical propositions on basis or research findings and experiences of others researching in related technological areas.
- Evaluate findings to develop new concepts, products, or processes, or to develop applications of findings to new uses.
- Write technical papers to be published in prestigious conferences and journals.
- Prepare technical reports for use by engineering or management personnel for long- and short-term planning.
Requirements:
- A PhD degree holder in Computer Science or related disciplines.
- Excellent verbal and written communication skills in English.
- Extensive knowledge in machine learning and AI algorithms, especially in natural language processing (NLP), speech recognition, and/or related areas is preferred.
- Strong mathematical/analytical foundation, problem solving skills.
- Experience in software developments for machine learning/AI algorithms are highly preferred.
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Research Scientist
Posted today
Job Viewed
Job Description
We are seeking a talented and motivated Research Scientist to join our Battery and Application Technology team. Help shape the future of battery technology by contributing to groundbreaking research and development projects.
Responsibilities
- Design and execute electrochemical tests on anode and cathode materials for aqueous battery systems.
- Develop advanced electrochemical diagnosis platforms and conduct in-situ testing on electrodes and components.
- Optimize charge-discharge and evaluation protocols to assess electrochemical performance.
- Explore and refine testing procedures for electrodes, electrolytes, and separators.
- Perform electrochemical cell teardowns and carry out failure analysis on battery materials and components.
- Visualize and analyze data, preparing comprehensive reports with actionable recommendations for battery additive R&D.
- Collaborate closely with research teams to guide promising scenarios toward production readiness.
Qualifications
- Ph.D. in Battery Chemistry, Electrochemistry, Material Chemistry, Material Physics, or a related discipline.
- 1 year of R&D experience in rechargeable battery research or energy storage materials is mandatory
- Proficiency in electrochemical testing techniques (e.g., CV, EIS, LSV, GITT), with proven ability to conduct independent R&D.
- Strong analytical and problem-solving skills, with a keen eye for data analysis and statistics.
- Excellent interpersonal and communication skills
- Strong sense of accountability, integrity, and results-oriented mindset
- Willingness to learn new concepts from patents and literature, and propose creative ideas
- Background in developing battery and inorganic materials, as well as familiarity with crystal structure analysis techniques (e.g., XRD) is preferred
- Experience with organic material development is preferred
- Frequent travel to PRC is required
For more company details, please visit our website at
If you are ready to drive innovation and make an impact in the world of battery technology, we would love to hear from you
We offer attractive remuneration package, 5-day work week and long-term career development opportunities to the right candidate. Please send your full resume with current and expected salary by clicking "Apply".
We are an equal opportunity employer. The information provided by you will be treated in strict confidence and used for recruitment purpose only. All personal data collected during the application process will be kept for 12 months after its completion, and will be destroyed thereafter.
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