136 Healthcare Project Management jobs in Hong Kong
Clinical Trials Assistant
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Guangzhou, China
Full time
R
Hybrid
Job available in additional locations
China
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Job Overview
Perform daily administrative activities, in conjunction with the Clinical Research Associates and Regulatory and Start-Up teams, to ensure a complete and accurate Trial Master File delivery.
Essential Functions
• Assist Clinical Research Associates (CRAs) and Regulatory and Start-Up (RSU) team with accurately updating and maintaining clinical documents and systems (e.g., Trial Master File (TMF)) that track site compliance and performance within project timelines.
• Assist the clinical team with the preparation, handling, distribution, filing, and archiving of clinical documentation and reports according to the scope of work and standard operating procedures.
• Assist with periodic review of study files for completeness.
• Assist CRAs and RSU with preparation, handling and distribution of Clinical Trial Supplies and maintenance of tracking information. Coordinate the tracking and management of Case Report Forms (CRFs), queries and clinical data flow.
• Act as a central contact for the clinical team for designated project communications, correspondence and associated documentation.
• May accompany CRAs on site visits to assist with clinical monitoring duties upon completion of required training.
• May collaborate with the clinical team on the preparation, handling, distribution, filing, and archiving of clinical documentation and reports according to the scope of work and standard operating procedures.
Qualifications
• High School Diploma or equivalent Req
• 3-4 years administrative support experience.
• r Equivalent combination of education, training and experience.
• Minimum one year clinical research experience strongly preferred.
• Computer skills including working knowledge of Microsoft Word, Excel and PowerPoint.
• Written and verbal communication skills including good command of English language.
• Effective time management and organizational skills.
• Ability to establish and maintain effective working relationships with coworkers, managers, and clients.
• Basic knowledge of applicable clinical research regulatory requirement, i.e., Good Clinical Practice (GCP) and International Conference on Harmonization (ICH) guidelines as provided in company training.
• Knowledge of applicable protocol requirements as provided in company training.
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
Clinical Trials Assistant (CTA) (Evergreen)
Posted 22 days ago
Job Viewed
Job Description
Join to apply for the Clinical Trials Assistant (CTA) (Evergreen) role at IQVIA
Clinical Trials Assistant (CTA) (Evergreen)1 day ago Be among the first 25 applicants
Join to apply for the Clinical Trials Assistant (CTA) (Evergreen) role at IQVIA
Job Overview
Perform daily administrative activities, in conjunction with the Clinical Research Associates and Regulatory and Start-Up teams, to ensure a complete and accurate Trial Master File delivery.
Job Overview
Perform daily administrative activities, in conjunction with the Clinical Research Associates and Regulatory and Start-Up teams, to ensure a complete and accurate Trial Master File delivery.
Essential Functions
- Assist Clinical Research Associates (CRAs) and Regulatory and Start-Up (RSU) team with accurately updating and maintaining clinical documents and systems (e.g., Trial Master File (TMF)) that track site compliance and performance within project timelines.
- Assist the clinical team with the preparation, handling, distribution, filing, and archiving of clinical documentation and reports according to the scope of work and standard operating procedures.
- Assist with periodic review of study files for completeness.
- Assist CRAs and RSU with preparation, handling and distribution of Clinical Trial Supplies and maintenance of tracking information.
- Assist with the tracking and management of Case Report Forms (CRFs), queries and clinical data flow.
- Act as a central contact for the clinical team for designated project communications, correspondence and associated documentation.
- May accompany CRAs on site visits to assist with clinical monitoring duties upon completion of required training.
- High School Diploma or equivalent Req.
- 3 years administrative support experience.
- Equivalent combination of education, training and experience.
- Computer skills including working knowledge of Microsoft Word, Excel and PowerPoint.
- Written and verbal communication skills including good command of English language.
- Effective time management and organizational skills.
- Ability to establish and maintain effective working relationships with coworkers, managers, and clients.
- Awareness of applicable clinical research regulatory requirements, i.e., Good Clinical Practice (GCP) and International Conference on Harmonization (ICH) guidelines as provided in company training.
- Knowledge of applicable protocol requirements as provided in company training.
- Seniority level Entry level
- Employment type Full-time
- Job function Research, Analyst, and Information Technology
- Industries Pharmaceutical Manufacturing
Referrals increase your chances of interviewing at IQVIA by 2x
Get notified about new Clinical Trial Assistant jobs in Kwai Tsing District, Hong Kong SAR .
Temporary Research Assistant I / Research Assistant II Part-time Research Assistant II (R6681) (S&T) Temporary Research Associate/Research Assistant I/Research Assistant IIHong Kong SAR HK$13,110.00-HK$13, hours ago
Temporary Research Assistant I / Research Assistant II - (25001HL) Research Assistant (Fresh Graduates Welcome) Temporary Research Associate/Research Assistant I/Research Assistant II - (25001HN)We’re unlocking community knowledge in a new way. Experts add insights directly into each article, started with the help of AI.
#J-18808-LjbffrClinical Trials Assistant (CTA) (Evergreen)

Posted 15 days ago
Job Viewed
Job Description
Perform daily administrative activities, in conjunction with the Clinical Research Associates and Regulatory and Start-Up teams, to ensure a complete and accurate Trial Master File delivery.
**Essential Functions**
- Assist Clinical Research Associates (CRAs) and Regulatory and Start-Up (RSU) team with accurately updating and maintaining clinical documents and systems (e.g., Trial Master File (TMF)) that track site compliance and performance within project timelines.
- Assist the clinical team with the preparation, handling, distribution, filing, and archiving of clinical documentation and reports according to the scope of work and standard operating procedures.
- Assist with periodic review of study files for completeness.
- Assist CRAs and RSU with preparation, handling and distribution of Clinical Trial Supplies and maintenance of tracking information.
- Assist with the tracking and management of Case Report Forms (CRFs), queries and clinical data flow.
- Act as a central contact for the clinical team for designated project communications, correspondence and associated documentation.
- May accompany CRAs on site visits to assist with clinical monitoring duties upon completion of required training.
**Qualifications**
- High School Diploma or equivalent Req.
- 3 years administrative support experience.
- Equivalent combination of education, training and experience.
- Computer skills including working knowledge of Microsoft Word, Excel and PowerPoint.
- Written and verbal communication skills including good command of English language.
- Effective time management and organizational skills.
- Ability to establish and maintain effective working relationships with coworkers, managers, and clients.
- Awareness of applicable clinical research regulatory requirements, i.e., Good Clinical Practice (GCP) and International Conference on Harmonization (ICH) guidelines as provided in company training.
- Knowledge of applicable protocol requirements as provided in company training.
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
Clinical Trials Assistant (CTA) (Evergreen)
Posted 23 days ago
Job Viewed
Job Description
Join to apply for the Clinical Trials Assistant (CTA) (Evergreen) role at IQVIA
Clinical Trials Assistant (CTA) (Evergreen)1 day ago Be among the first 25 applicants
Join to apply for the Clinical Trials Assistant (CTA) (Evergreen) role at IQVIA
Job Overview
Perform daily administrative activities, in conjunction with the Clinical Research Associates and Regulatory and Start-Up teams, to ensure a complete and accurate Trial Master File delivery.
Job Overview
Perform daily administrative activities, in conjunction with the Clinical Research Associates and Regulatory and Start-Up teams, to ensure a complete and accurate Trial Master File delivery.
Essential Functions
- Assist Clinical Research Associates (CRAs) and Regulatory and Start-Up (RSU) team with accurately updating and maintaining clinical documents and systems (e.g., Trial Master File (TMF)) that track site compliance and performance within project timelines.
- Assist the clinical team with the preparation, handling, distribution, filing, and archiving of clinical documentation and reports according to the scope of work and standard operating procedures.
- Assist with periodic review of study files for completeness.
- Assist CRAs and RSU with preparation, handling and distribution of Clinical Trial Supplies and maintenance of tracking information.
- Assist with the tracking and management of Case Report Forms (CRFs), queries and clinical data flow.
- Act as a central contact for the clinical team for designated project communications, correspondence and associated documentation.
- May accompany CRAs on site visits to assist with clinical monitoring duties upon completion of required training.
- High School Diploma or equivalent Req.
- 3 years administrative support experience.
- Equivalent combination of education, training and experience.
- Computer skills including working knowledge of Microsoft Word, Excel and PowerPoint.
- Written and verbal communication skills including good command of English language.
- Effective time management and organizational skills.
- Ability to establish and maintain effective working relationships with coworkers, managers, and clients.
- Awareness of applicable clinical research regulatory requirements, i.e., Good Clinical Practice (GCP) and International Conference on Harmonization (ICH) guidelines as provided in company training.
- Knowledge of applicable protocol requirements as provided in company training.
- Seniority level Entry level
- Employment type Full-time
- Job function Research, Analyst, and Information Technology
- Industries Pharmaceutical Manufacturing
Referrals increase your chances of interviewing at IQVIA by 2x
Get notified about new Clinical Trial Assistant jobs in Kwai Tsing District, Hong Kong SAR .
Temporary Research Assistant I / Research Assistant II Part-time Research Assistant II (R6681) (S&T) Temporary Research Associate/Research Assistant I/Research Assistant IIHong Kong SAR HK$13,110.00-HK$13, hours ago
Temporary Research Assistant I / Research Assistant II - (25001HL) Research Assistant (Fresh Graduates Welcome) Temporary Research Associate/Research Assistant I/Research Assistant II - (25001HN)We’re unlocking community knowledge in a new way. Experts add insights directly into each article, started with the help of AI.
#J-18808-LjbffrProject Planning Manager
Posted today
Job Viewed
Job Description
- Develop and manage comprehensive project schedules for E&M works using tools such as Primavera P6 or MS Project.
- Coordinate with multidisciplinary teams including civil, structural, architectural, and systems engineering to ensure integrated planning.
- Monitor project progress, identify risks and delays, and propose mitigation strategies.
- Lead planning meetings and workshops with internal and external stakeholders.
- Prepare and present planning reports, dashboards, and progress updates to senior management and clients.
- Ensure compliance with contractual requirements, safety standards, and regulatory guidelines.
- Support tendering and procurement processes by providing planning input and resource analysis.
- Collaborate with site teams to ensure alignment between construction activities and project timelines.
- Bachelor's degree in Electrical, Mechanical, or Civil Engineering, or related discipline.
- Minimum 8–10 years of experience in project planning, with at least 5 years in large-scale infrastructure projects (e.g., rail, airport, utilities, tunnels).
- Proficiency in planning software such as Primavera P6, MS Project, and Excel.
- Strong understanding of E&M systems including HVAC, fire services, electrical distribution, and plumbing.
- Excellent communication, leadership, and stakeholder management skills.
- PMP or similar project management certification is a plus.
Engineer / Assistant Engineer - Project Planning
Posted today
Job Viewed
Job Description
Chevalier (HK) Limited provides installation, testing, repair, maintenance, and modernization services of lifts and escalators. We participate in different kinds of development projects consisting of commercial buildings, hotels, private residential estates and public housing projects etc. Established in 1970, the lift and escalator division was Chevalier's first business division and today it remains one of our core businesses.
Responsibilities
- Provide technical support in installation and modernization design works of lifts and escalator projects
- Prepare relevant project correspondences including technical specification, quotation, shop drawings, etc
- Maintain close communications with vendors and factory
- Conduct site visit and meetings with architects and consultants
Requirements
- Degree holder in Mechanical / Electrical / Electronic / Building Services Engineering
- 1 year of relevant experience in E&M field
- Good command of both written and spoken English and Chinese
- Proficient in MS Office application (Word, Excel, Powerpoint), AutoCAD and Chinese Word Processing
- Candidates with more working experience will be considered for the position of Engineer
Benefits
- 5-Day Work Week
- Year End Bonus
- Medical Insurance
- Education Allowance
- Paid Annual Leave
- Paid Sick Leave
- Paid Marriage Leave & Marriage Gift
- New Born Baby Gift
- Scholarship for Employee's Children
We offer HKIE Graduate Training Scheme 'A' in Control, Automation & Instrumentation discipline to right candidate.
Attractive remuneration package will be offered to the right candidate. Interested parties, please send us your resume with current and expected salary by clicking "Apply Now" or mail to: The Human Resources Manager, Chevalier Group, 22/F, Chevalier Commercial Centre, 8 Wang Hoi Road, Kowloon Bay, Hong Kong
We are an equal opportunity employer and welcome applications from all qualified candidates. Personal data collected would be used for recruitment purpose only.
Engineer / Assistant Engineer - Project Planning
Posted today
Job Viewed
Job Description
Chevalier (HK) Limited provides installation, testing, repair, maintenance, and modernization services of lifts and escalators. We participate in different kinds of development projects consisting of commercial buildings, hotels, private residential estates and public housing projects etc. Established in 1970, the lift and escalator division was Chevalier's first business division and today it remains one of our core businesses.
Responsibilities
- Provide technical support in installation and modernization design works of lifts and escalator projects
- Prepare relevant project correspondences including technical specification, quotation, shop drawings, etc
- Maintain close communications with vendors and factory
- Conduct site visit and meetings with architects and consultants
Requirements
- Degree holder in Mechanical / Electrical / Electronic / Building Services Engineering
- 1 year of relevant experience in E&M field
- Good command of both written and spoken English and Chinese
- Proficient in MS Office application (Word, Excel, Powerpoint), AutoCAD and Chinese Word Processing
- Candidates with more working experience will be considered for the position of Engineer
Benefits
- 5-Day Work Week
- Year End Bonus
- Medical Insurance
- Education Allowance
- Paid Annual Leave
- Paid Sick Leave
- Paid Marriage Leave & Marriage Gift
- New Born Baby Gift
- Scholarship for Employee's Children
We offer HKIE Graduate Training Scheme 'A' in Control, Automation & Instrumentation discipline to right candidate.
Attractive remuneration package will be offered to the right candidate. Interested parties, please send us your resume with current and expected salary by clicking "Apply Now" or mail to: The Human Resources Manager, Chevalier Group, 22/F, Chevalier Commercial Centre, 8 Wang Hoi Road, Kowloon Bay, Hong Kong
We are an equal opportunity employer and welcome applications from all qualified candidates. Personal data collected would be used for recruitment purpose only.
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Engineer / Assistant Engineer - Project Planning
Posted today
Job Viewed
Job Description
Engineer / Assistant Engineer - Project Planning(Ref. No.:CHK/OPR/AE)
Responsibilities
Provide technical support in installation and modernization design works of lifts and escalator projects
Prepare relevant project correspondences including technical specification, quotation, shop drawings, etc
Maintain close communications with vendors and factory
Conduct site visit and meetings with architects and consultants
Requirements
Degree holder in Mechanical / Electrical / Electronic / Building Services Engineering
1 year of relevant experience in E&M field
Good command of both written and spoken English and Chinese
Proficient in MS Office application (Word, Excel, Powerpoint), AutoCAD and Chinese Word Processing
Candidates with more working experience will be considered for the position of Engineer
APPLY NOW
Please apply with full resume and expected salary to: (Please include the job title and reference number in the subject line) or Human Resources Manager, Chevalier Group, 22/F, Chevalier Commercial Centre, 8 Wang Hoi Road, Kowloon Bay, Hong Kong.
We are an equal opportunity employer and welcome applications from all qualified candidates. Personal data collected would be used for recruitment purpose only.
Project Engineer – Airport Planning
Posted today
Job Viewed
Job Description
ADP Ingenierie becomes Artelia Airports To strengthen our teams in the Hong Kong Business Unit, we are looking for a Project Engineer - Airport Planning.
Missions :
The Project Engineer:
- is expected to conduct airport planning exercises for regional projects, by applying their technical know-how, industry recognized benchmark data, codes and regulations
- has the flexibility to evolve in different geographical environments, is mobile for missions abroad and has the capability to adapt to the local context
Responsibilities
- analyze the necessary data and clients' objectives/requirements
- conduct integrated airport planning approaches and define the possible planning strategies for the airports
- performs airport planning technical studies, in compliance with standards and best practices: Basic market analysis / traffic forecast analysis
- Airport system capacity analysis and define program requirements
- Assist architects / master planners on airport related functional layout design
- Business plan / investments costs assessment
- Deliverables production including studies, notes, reports, presentations, etc.
- act as project coordinator to liaise with clients and partners liaison and coordinate with other internal and external experts
- contribute to the our Airport Planning Practice via development and update of tools and methodologies
- keeps up to date with latest industry trends and data
- participates in proposal preparations
Qualifications and Experiences
- Bachelor or Master's Degree in Engineering or Science or equivalent
- Strong analytical and problem solving skills and capable to exercise independent judgement
- Capable to work independently and in a multidisciplinary team
- Eager to learn with strong interest for the airport industry
- Conversant with ICAO/IATA regulation from previous experience is a plus
- Excellent writing / presentation skills
- Proficient in Microsoft Office package in particularly Excel and capable to handle large quantity of data efficiently and accurately
- Proficient in English written and spoken; ability in another language is a plus (Mandarin and/or other Asian languages are preferred)
- Candidate possessing additional skills in one or more of the following fields will be strongly preferred: Traffic forecasting (annual, peak hour, flight schedules), Financial analysis, Flow simulation (CAST, ARCPORT, Airtop or equivalent)
Note to external recruiters: Please note that Artelia Airports does not accept unsolicited resumes from recruiters or employment agencies. In the absence of a signed Recruitment Fee Agreement, Artelia Airportswill not consider or agree to payment of any referral compensation or recruiter fee. In the event a recruiter or agency submits a resume or candidate without a previously signed agreement, Artelia Airports explicitly reserves the right to pursue and hire those candidate(s) without any financial obligation to the recruiter or agency. Any unsolicited resumes, including those submitted to hiring managers, are deemed to be the property of Artelia Airports and no fee will be paid in the event the candidate is hired by Artelia Airports as a result of the referral or through other means.
Store Planning Project Manager
Posted today
Job Viewed
Job Description
Position
This role is responsible for retail projects operational phases, organization and implementation (new openings, expansion, renovation, relocation, maintenance, etc.). She/he monitors projects' progress, ensuring cost effective flows of materials and liaising with the external Architectural Firms involved.
Responsibilities
Project Planning
- Ensures that the Store Planning Projects are delivered on-time, within scope and within budget:
- Monitors project status and anticipates completion dates
- Is responsible for projects cost monitoring (preliminary analysis, offers comparison, verify the implementation of price list, etc.)
- Prepares cost reports and regular updates during the project development
- Implements the construction and opening plan.
Design and Construction
- Work on feasibility analysis concerning sizing and adequacy of the premises.
- Visit construction sites monitoring the working progress, ensure timing to be compliant with the schedule and to handle issues and critical situations.
- Act as the point of reference with other Functions and external suppliers involved in the project regarding all the operational phases.
Operations
Oversees quality procedures and implements policies and to ensure conformity with Company and legal requirements. Updates the Stores projects archive
Skills and abilities required:
- Degree in Architecture, Engineering, Construction or equivalent experience.
- Minimum 5 years' experience as Project Manager in store planning or construction environment preferably in luxury industry.
- Ability to effectively interface with all key internal/external stakeholders.
- Proven project management skills (coordination, communication, budget management, goals achievement, prioritization, troubleshooting, etc…).
- Results-oriented.
- Strong analytical skills.
- Strong interpersonal skills and organizational savvy.
- Multi-projects management skills.
- Flexible and dynamic team player.
- Excellent knowledge of Microsoft Office and Autocad.