28 Healthcare Specialist jobs in Hong Kong

二級病人服務助理 (門診/病房/急症門診) Patient Care Assistant II (In-Patient/ Out-Patient/ Emergency Medicine Centre)

職責:

• 處理一般門診/病房服務流程: 例如接待病人、量度維生指數、床邊護理、預約登記、整理病歷及基本收費服務
• 協助醫生和護士為病人執行日常檢查工作和診症
• 提供優質客戶服務

入職要求:

• 中五或以上程度
• 須具備相關工作經驗
• 須持有醫護支援人員訓練或相關課程證書
• 能操流利粵語,略懂英語、普通話及電腦操作
• 工作時間按各部門而定 , 通常每更工作時間約7小時
• 提供在職訓練及持續進修培訓
• 如工作表現優良及符合入讀資格,可保薦升讀本院之登記護士課程

員工可享有有薪年假、銀行假期、在職培訓、住院保險、門診津貼、渡假屋等福利。

求職者可在本院網站 ( (link removed) ) 下載職位申請表 (請寫上職位編號), 並連同證明文件經以下途徑遞交:

郵寄: 新界沙田大圍富健街十八號仁安醫院人力資源部收 或 電郵: Apply Now 或 傳真:

註一:所收集的資料只作招聘用途。

註二:若申請人於兩個月內仍未收到任何通知,則當自動落選;半年內已遞交同一職位申請之人士,無須再遞交申請表。

註三:因應「性罪行定罪紀錄查核」機制已實施,本院將會要求有關職位的準僱員進行性罪行定罪紀錄查核。

二級病人服務助理 (門診/病房/急症門診) Patient Care Assistant II (In-Patient/ Out-Patient/ Emergency Medicine Centre)

職責:

• 處理一般門診/病房服務流程: 例如接待病人、量度維生指數、床邊護理、預約登記、整理病歷及基本收費服務
• 協助醫生和護士為病人執行日常檢查工作和診症
• 提供優質客戶服務

入職要求:

• 中五或以上程度
• 須具備相關工作經驗
• 須持有醫護支援人員訓練或相關課程證書
• 能操流利粵語,略懂英語、普通話及電腦操作
• 工作時間按各部門而定 , 通常每更工作時間約7小時
• 提供在職訓練及持續進修培訓
• 如工作表現優良及符合入讀資格,可保薦升讀本院之登記護士課程

員工可享有有薪年假、銀行假期、在職培訓、住院保險、門診津貼、渡假屋等福利。

求職者可在本院網站 ( (link removed) ) 下載職位申請表 (請寫上職位編號), 並連同證明文件經以下途徑遞交:

郵寄: 新界沙田大圍富健街十八號仁安醫院人力資源部收 或 電郵: Apply Now 或 傳真:

註一:所收集的資料只作招聘用途。

註二:若申請人於兩個月內仍未收到任何通知,則當自動落選;半年內已遞交同一職位申請之人士,無須再遞交申請表。

註三:因應「性罪行定罪紀錄查核」機制已實施,本院將會要求有關職位的準僱員進行性罪行定罪紀錄查核。

At Transmedic, a company of EBOS Med Tech, we believe healthcare professionals and patients should have access to world-leading medical devices, whilst ensuring long-term economic sustainability within the healthcare system. As a leading independent distributor of medical technology, we bring innovative medical solutions to healthcare professionals by partnering with world leading companies who share our vision for innovation.

Key Responsibilities

• Provide clinical support & trouble shooting of medical equipment to healthcare professionals
• Assist healthcare professionals to become familiarized with the medical equipment in terms of product's features and usage
• Responsible for developing, building, and strengthening long-term collaborations including distributors and healthcare professionals
• Organize and conduct training to healthcare professionals to improve the benefits derived from products and/or services
• Provide prompt response to product and service enquiries, and take thorough follow-up actions on outstanding issues
• Communicate customer feedback on existing products and potential new product development to company

Pre-Requisites (Qualifications & Experience)

• Possess a diploma or above
• Fresh graduates are welcome to apply
• Candidates with previous experience in sales / technical support on medical devices will have added advantage
• Candidates with more experience may be considered for a senior position
• Knowledge of the Operating Room environment is highly preferable
• Good interpersonal and communication skills
• Highly motivated and result-oriented

More about Transmedic

Transmedic - Where the world's leading healthcare solutions meet the needs of our people.

We open the door to a world of healthcare solutions, connecting professionals and organisations in Asia with leading medical specialty products, local knowledge and personalised service to advance the quality of care for patients who need it most.

We take pride in being different. We put our customers at the heart of everything we do, stay nimble and adaptable, strive for excellence, and foster a team that's passionate and driven.

About Our Client

Our client is an international medical manufacturer known for producing top-notch medical technologies that has been curing patients around the world. To cope with their further expansion in APAC, they would like to invite a high calibre individual to join their professional teams as a clinical specialist.

About the Role:

• Provide training and education for both internal personnel and healthcare professionals with up-to-date information about signature products
• Liaising with medical practitioners and other healthcare professionals to maintain a close relationship and reputable company image
• Plan and implement Peer to peer training, case coverage, new hire training and new product development training
• Coordinate a team of clinical educators to help with product education
• Provide approved educational material and content in compliance with Off Label and Promotion Activities Policies

The Successful Applicant:

• Bachelor degree or above in a clinical and science-based field, or a degree in nursing
• A minimum of 3 years of medical professional training or clinical operations in hospital settings
• Clinical mastery related to medical devices
• Of independent and analytical character with professional work ethics and strong organisational skills
• Strong interpersonal skill and experience of training healthcare professionals
• Adept MS office skills for report and spreadsheet compilation, as well as presentations

Click "Apply * *Now* *" to apply for this position or call Stanley Leung at for a confidential discussion. All information collected will be kept in strict confidence and will be used for recruitment purpose only.

Overview

Join to apply for the Clinical Trial Specialist role at Emerald Clinical .

At Emerald Clinical Trials , we are a global, full-service Contract Research Organization (CRO) with a presence in the Asia-Pacific region. We support biopharmaceutical, medical device, and diagnostic customers across all trial phases, from registration to post-marketing.

Our therapeutic expertise spans renal , cardiometabolic , and oncology , areas where we make a meaningful impact on global health.

The Clinical Trial Specialist (CTS) is a member of the Clinical Operations team responsible for supporting clinical trial activities as the in-house site start-up and maintenance specialist. The CTS works with the project team to ensure trials are conducted in accordance with Federal Regulations, ICH guidelines, project plans, IRB/ Ethics Committee requirements, and applicable SOPs and guidelines. The CTS assists with feasibility, start-up activities, and collection of essential documents for site initiation, submissions to central IRBs/Ethics Committees, and changes to Informed Consent Forms (ICFs).

• Increase proficiency in Trial Master File (TMF) set-up and maintenance (filing), both hard copy and electronic as assigned by project.
• Upload and maintain TMF files and folders in Emerald Clinical’s file-sharing system by project as assigned.
• Serve as second reviewer for TMF QC.
• May function as TMF Lead, taking responsibility for TMF setup, maintenance and oversight.
• Assist with/end of study TMF filing (including site close-out documents), QC and archival.
• Develop skills in preparing and participating in audit responses.
• Perform QC of documents and emails prior to sending to ensure quality deliverables.
• Develop skills in data entry and maintaining files/folders for Clinical Trial Management System by project.
• Support data entry, tracking and submission for investigator payments by project.
• Collaborate with CRA/CTM/PM during site start-up for feasibility, acting as point of contact for sites where applicable.
• Assist in presenting final feasibility results to PM team and/or Sponsor.
• Assist sites in preparing, planning, organizing and collecting essential document packets (EDPs).
• Submit final EDPs to sponsor or CTM/PM as required.

• College/University diploma/degree; or at least 2 years related experience and/or training; or equivalent combination of education and experience.
• Ability to perform general administrative duties as needed.
• Exposure to medical terminology preferred.
• Knowledge of ICH/GCP, ethical and regulatory requirements preferred.

At our core, Emerald Clinical Trials is committed to transforming clinical research by putting people first—patients and employees. You’ll be part of a global network of professionals delivering better research and outcomes for millions worldwide.

Here’s what makes us stand out:

• Purpose-Driven Work : Contribute to clinical trials that improve lives in renal, cardiometabolic, and oncology areas.
• Global Reach, Local Expertise : Connect with local communities for trusted trial engagement.
• Collaboration and Innovation : A culture of diverse perspectives and creative solutions.

We provide a supportive environment with:

• Competitive Compensation : Tailored salary and benefits to reflect your skills and experience.
• Career Growth : Learning opportunities within a global network of scientific leaders.
• Employee Wellbeing : Programs promoting work-life balance, health, and team connection.
• Global Opportunities : Exposure to international projects and clients.

Interested? Apply now and help us improve health worldwide.

We are an equal-opportunity employer and encourage applications from all qualified candidates.

Overview

At Emerald Clinical Trials , we are a global, full-service Contract Research Organization (CRO) with a rich heritage in the Asia-Pacific region. We are dedicated to advancing clinical research through scientific expertise and operational excellence, supporting biopharmaceutical, medical device, and diagnostic customers across all trial phases, from registration to post-marketing. Our therapeutic expertise spans renal , cardiometabolic , and oncology —areas where we make a significant impact on improving global health. At the heart of our success is our ability to combine global reach with local knowledge. Our on-the-ground teams work closely with local communities, building trust and ensuring diverse, representative patient recruitment. By prioritizing people, we deliver better engagement, more accurate data, and faster results—bringing therapies to patients in need.

About The Role

The Clinical Trial Specialist (CTS) is a member of the Clinical Operations team responsible for supporting clinical trial activities as the in-house site start-up and maintenance specialist. As part of the clinical trial project team, the CTS is responsible for ensuring clinical trials are conducted according to Federal Regulations, ICH guidelines, appropriate project plans, IRB/Ethic Committee requirements, and applicable SOPs and guidelines. The CTS works closely with the project team to help manage clinical trial feasibility processes, coordinate clinical trial start-up activities including collection of essential documents for site initiation/startup, submissions to central IRBs/Ethic Committees, supporting site staff in the submission to local IRBs/Ethic Committees and changes to Informed Consent Forms (ICFs).

At Emerald Clinical Trials , we are a global, full-service Contract Research Organization (CRO) with a rich heritage in the Asia-Pacific region. We are dedicated to advancing clinical research through scientific expertise and operational excellence, supporting biopharmaceutical, medical device, and diagnostic customers across all trial phases, from registration to post-marketing. Our therapeutic expertise spans renal , cardiometabolic , and oncology —areas where we make a significant impact on improving global health. At the heart of our success is our ability to combine global reach with local knowledge. Our on-the-ground teams work closely with local communities, building trust and ensuring diverse, representative patient recruitment. By prioritizing people, we deliver better engagement, more accurate data, and faster results—bringing therapies to patients in need.

About The Role

The Clinical Trial Specialist (CTS) is a member of the Clinical Operations team responsible for supporting clinical trial activities as the in-house site start-up and maintenance specialist. As part of the clinical trial project team, the CTS is responsible for ensuring clinical trials are conducted according to Federal Regulations, ICH guidelines, appropriate project plans, IRB/Ethic Committee requirements, and applicable SOPs and guidelines. The CTS works closely with the project team to help manage clinical trial feasibility processes, coordinate clinical trial start-up activities including collection of essential documents for site initiation/startup, submissions to central IRBs/Ethic Committees, supporting site staff in the submission to local IRBs/Ethic Committees and changes to Informed Consent Forms (ICFs).

Join to apply for the Clinical Trial Specialist role at Emerald Clinical .

At Emerald Clinical Trials , we are a global, full-service Contract Research Organization (CRO) with a presence in the Asia-Pacific region. We support biopharmaceutical, medical device, and diagnostic customers across all trial phases, from registration to post-marketing.

Our therapeutic expertise spans renal , cardiometabolic , and oncology , areas where we make a meaningful impact on global health.

The Clinical Trial Specialist (CTS) is a member of the Clinical Operations team responsible for supporting clinical trial activities as the in-house site start-up and maintenance specialist. The CTS works with the project team to ensure trials are conducted in accordance with Federal Regulations, ICH guidelines, project plans, IRB/ Ethics Committee requirements, and applicable SOPs and guidelines. The CTS assists with feasibility, start-up activities, and collection of essential documents for site initiation, submissions to central IRBs/Ethics Committees, and changes to Informed Consent Forms (ICFs).

• Increase proficiency in Trial Master File (TMF) set-up and maintenance (filing), both hard copy and electronic as assigned by project.
• Upload and maintain TMF files and folders in Emerald Clinical’s file-sharing system by project as assigned.
• Serve as second reviewer for TMF QC.
• May function as TMF Lead, taking responsibility for TMF setup, maintenance and oversight.
• Assist with/end of study TMF filing (including site close-out documents), QC and archival.
• Develop skills in preparing and participating in audit responses.
• Perform QC of documents and emails prior to sending to ensure quality deliverables.
• Develop skills in data entry and maintaining files/folders for Clinical Trial Management System by project.
• Support data entry, tracking and submission for investigator payments by project.
• Collaborate with CRA/CTM/PM during site start-up for feasibility, acting as point of contact for sites where applicable.
• Assist in presenting final feasibility results to PM team and/or Sponsor.
• Assist sites in preparing, planning, organizing and collecting essential document packets (EDPs).
• Submit final EDPs to sponsor or CTM/PM as required.

• College/University diploma/degree; or at least 2 years related experience and/or training; or equivalent combination of education and experience.
• Ability to perform general administrative duties as needed.
• Exposure to medical terminology preferred.
• Knowledge of ICH/GCP, ethical and regulatory requirements preferred.

At our core, Emerald Clinical Trials is committed to transforming clinical research by putting people first—patients and employees. You’ll be part of a global network of professionals delivering better research and outcomes for millions worldwide.

Here’s what makes us stand out:

• Purpose-Driven Work : Contribute to clinical trials that improve lives in renal, cardiometabolic, and oncology areas.
• Global Reach, Local Expertise : Connect with local communities for trusted trial engagement.
• Collaboration and Innovation : A culture of diverse perspectives and creative solutions.

We provide a supportive environment with:

• Competitive Compensation : Tailored salary and benefits to reflect your skills and experience.
• Career Growth : Learning opportunities within a global network of scientific leaders.
• Employee Wellbeing : Programs promoting work-life balance, health, and team connection.
• Global Opportunities : Exposure to international projects and clients.

Interested? Apply now and help us improve health worldwide.

We are an equal-opportunity employer and encourage applications from all qualified candidates.

Job Description:

We are seeking two detailed-oriented and proactive Clinical Trial Specialists to lead community health initiatives with local resources to improve chronic disease management, prevention, and education. This role involves strategic collaboration between Hong Kong and Mainland China, requiring occasional travel to align with organizational goals. If you are passionate about biomedical innovation and public health, we invite you to join our dynamic team.

Responsibilities:

• Program Development & Data Management: Design, implement, and oversee data-driven health programs (e.g., cardiovascular disease prevention).

• Stakeholder Collaboration: Partner with hospitals, NGOs, and community organizations to strengthen referral networks and resource integration.

• Training & Capacity Building: Educate healthcare providers and patients on chronic disease management, digital health tools (e.g., AI, remote monitoring), and best practices.

• Performance & Compliance: Monitor programme effectiveness, analyse outcomes, and ensure adherence to regulatory standards (ICH-GCP & local healthcare laws).

• Perform other duties as assigned to advance COCHE's mission.

General Qualification:

Education:

• Master's degree or higher in Medicine, Public Health, Nursing, or a related field preferred.

Experience:

• Minimum 3 years in community health programs, with expertise in risk assessment and intervention strategies.

Skills & Competencies:

1. Fluency in English and Chinese (Cantonese proficiency is a plus).

1. Proficiency in data analysis tools (SPSS, Excel) and familiarity with health IT systems/digital healthcare applications.

2. Strong strategic thinking, adaptability to cross-cultural environments, and willingness to travel (~25% of time).

3. Excellent communication and interpersonal skills, with experience engaging diverse stakeholders.