3 Clinical Safety jobs in Hong Kong
Patient Safety Partner
Posted 6 days ago
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Job Description
Join to apply for the Patient Safety Partner role at Roche
1 day ago Be among the first 25 applicants
Join to apply for the Patient Safety Partner role at Roche
At Roche you can show up as yourself, embraced for the unique qualities you bring. Our culture encourages personal expression, open dialogue, and genuine connections, where you are valued, accepted and respected for who you are, allowing you to thrive both personally and professionally. This is how we aim to prevent, stop and cure diseases and ensure everyone has access to healthcare today and for generations to come. Join Roche, where every voice matters.
The Position
Roche Pharmaceuticals
Job Purpose
Support the implementation, maintenance and oversight of the local PV system for the assigned affiliate(s)/country(ies), to ensure an efficient and effective PV system that complies with global Roche and local legal/regulatory authority PV requirements, safeguarding our License to Operate.
Support the execution of IPS & Affiliate’s Patient Safety (APS) strategies, ensuring high-quality implementation of global and local safety solutions, while demonstrating leadership in ownership, collaboration, and decision-making within assigned responsibilities.
Key Responsibilities
PV System
- Execution of safety-related activities relevant to the PV system through partnership with key stakeholders such as Patient Safety Operations and Affiliate PV Net, to ensure monitoring of the safety profile of Roche products and their safety risk management, meet regulatory requirements, and ensure license to operate. Proactively identify opportunities to optimize the PV system
- Individual Case Safety Reports (e.g. data collection and reporting to HA)
- Signal Detection & Signal Management for Local Products
- Aggregate safety reports (e.g. data collection and submission to HA)
- Pharmacovigilance Agreements (e.g. PVA, Safety Data Exchange Agreement)
- Risk Management and Safety Communication (e.g., Direct Healthcare Professional Communication, Risk Minimization Measures, emerging safety issues)
- Studies, Programs and other projects with PV implications (e.g., ICT, NIS, PASS, PAES, MAP, PAA, CUP, PTAP, Dicela)
- Safety Labeling and PV Commitments
- Local Pharmacovigilance System Master File
- As a contributor, shape country PV regulations and the broader country pharmacovigilance ecosystem according to APS grouping, in particular in order to promote regulatory reliance and international harmonization in partnership with, and not limited to, local pharma industry associations, healthcare organizations, patient groups etc, where applicable.
- Generate and share safety insights by understanding disease areas (Roche portfolio, patient journey), engaging with key stakeholders, and ensuring timely, proactive integration into Affiliate and global strategies
- Implementation of safety solutions and launch readiness activities: Implement global safety solutions locally within the integrated therapeutic strategy, and execute product safety launch readiness activities
- Risk management and safety communication: Support the country-level risk management strategy to optimize patient outcomes in collaboration within relevant networks and ensure compliant and transparent PV communications (e.g., DHPCs) to healthcare professionals, patients, and external partners in collaboration with in collaboration with Medical Affairs and the cross-functional team
Education/Qualifications
- Qualification and/or Degree in life science or healthcare-related discipline (e.g., PharmD, Pharmacy, Nursing, Medicine, Master of Science, Bachelor of Science, etc.)
- 1-3 years experience in pharmacovigilance, ideally in an affiliate setting
- Understanding of decision-making in the local & global PV ecosystem
- Advantage: Experience in other affiliate medical functions (e.g., Medical Affairs, Clinical Operations, Medical Information) or global functions such as Clinical Safety
Strategic Thinking & Planning
- Understands the basics of strategic planning and its importance
- Pro-active and strategic mindset; able to think in systems and plan for outcomes
- Is able to update own and team objectives/actions to reflect changing circumstances and to influence strategy on local projects
- Focuses on the basics of execution: can understand project fundamentals, contribute to plans, manage their own tasks, communicate basic information, and recognize potential issues, solve problems, and report progress comprehensively
- Actively contributes ideas and expertise to network projects
- Shares experiences and best practices that benefit the network
- Influence to gain support for initiatives from cross-functional teams
- Understands the structure, key roles and responsibilities of internal stakeholders and builds trusting relationships
- Communicates timely and effectively
- Abundance mindset, thinking beyond one's role and team and looking at wider opportunities and impact
- Solves problems within own discipline and removes obstacles
- Prioritizes own work in support of global and local priorities to create clarity and focus
- Ability to seek information to understand high level drug development
- Basic understanding of drug development, pharmaceutical industry
- Understands regulatory requirements and integrates them into daily activities
- Can clearly speak about process during an audit or inspection
- Seeks feedback on their performance and grows confidence in providing appropriate feedback to others
A healthier future drives us to innovate. Together, more than 100’000 employees across the globe are dedicated to advance science, ensuring everyone has access to healthcare today and for generations to come. Our efforts result in more than 26 million people treated with our medicines and over 30 billion tests conducted using our Diagnostics products. We empower each other to explore new possibilities, foster creativity, and keep our ambitions high, so we can deliver life-changing healthcare solutions that make a global impact.
Let’s build a healthier future, together.
Roche is an Equal Opportunity Employer. Seniority level
- Seniority level Mid-Senior level
- Employment type Full-time
- Job function Research, Science, and Engineering
- Industries Pharmaceutical Manufacturing, Biotechnology Research, and Medical Equipment Manufacturing
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#J-18808-LjbffrClinical Trials Assistant (CTA) (Evergreen)
Posted 27 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.
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Clinical Trials Assistant (CTA) (Evergreen)
Posted 4 days ago
Job Viewed
Job Description
Join to apply for the Clinical Trials Assistant (CTA) (Evergreen) role at IQVIA
Clinical Trials Assistant (CTA) (Evergreen)2 weeks ago Be among the first 25 applicants
Join to apply for the Clinical Trials Assistant (CTA) (Evergreen) role at IQVIA
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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.
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 Not Applicable
- Employment type Full-time
- Job function Research, Analyst, and Information Technology
- Industries Pharmaceutical Manufacturing
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Sign in to set job alerts for “Clinical Trial Assistant” roles. Clinical Research Associate II (Hong Kong) Part-time Research Assistant II (N&HS) - (25001EZ) Research Assistant I/II (Ref.: H01/2025/067)Kwai Tsing District, Hong Kong SAR 1 day ago
Clinical Research Associate II（FSP, Client office-base)We’re unlocking community knowledge in a new way. Experts add insights directly into each article, started with the help of AI.
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