clinical research associate hong kong

Clinical Research Associate jobs in Hong Kong

Clinical research associate - fsp, research associate/post-doctoral fellow in nlp for clinical medicine.

Laboratory of Data Discovery for Health Limited

Clinical Associate/Assistant Professor of Practice in the Department of Obstetrics and Gynaecology

• Pok Fu Lam, Hong Kong

Clinical Associate/Assistant Professor of Practice

The University of Hong Kong

Sr Clinical Contracts and Budgets Associate

Tenure-track clinical professor/clinical associate professor in restorative dental sciences, associate professor (clinical).

The Chinese University of Hong Kong

Tenure-Track Clinical Associate Professor/ Clinical Assistant Professor

Clinical associate professor of practice in cardiology, tenure-track clinical associate professor/clinical assistant professor (several posts), non-tenure-track clinical associate professor, clinical professor/clinical associate professor in restorative dental sciences, professor / associate professor / assistant professor (clinical), clinical associate professor/ clinical assistant professor in the department of obstetrics, clinical associate in medical laboratory science.

The Hong Kong Polytechnic University

• Hung Hom, Hong Kong

Clinical Associate Professor/Clinical Assistant Professor in the LKS Faculty of Medicine

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Clinical Research Associate

• Location: Hong Kong
• Categories Clinical Monitoring
• __vacancyopjusttionswidget.opt-Business Area__ ICON Strategic Solutions
• __vacancyopjusttionswidget.opt-Remote Working __ Office Based

TA Business Partner

• Icon Strategic Solutions

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About the role, this vacancy has now expired. please see similar roles below....

Job Title: CRA

Working model: Office based in TOP 10 global pharma

ICON plc is a world-leading healthcare intelligence and clinical research organisation. From molecule to medicine, we advance clinical research providing outsourced services to pharmaceutical, biotechnology, medical device and government and public health organisations. With our patients at the centre of all that we do, we help to accelerate the development of drugs and devices that save lives and improve quality of life. Our people are our greatest strength, are at the core of our culture, and the driving force behind our success. ICON people have a mission to succeed and a passion that ensures what we do, we do well.

What you will be doing:

Clinical Research Associate is ultimately responsible for the successful management of investigator sites throughout the trial lifecycle.

Key responsibilities include:

• Developing effective relationships with investigator site staff to ensure that key clinical metrics are met.
• Preparing for and attending investigator meetings, coordinating the timely shipment and the subsequent proper storage and accountability of clinical supplies and following-up of drug safety issues.
• Ensuring integrity of clinical data through an ability to sufficiently maintain site tracking records and work diligently to relevant guidelines
• Negotiation and on-going management of clinical trial agreements with investigative sites

We believe our Clinical Operations team is second to none. You will receive the support you need to develop personally and professionally and work in an environment where you matter. Our team pushes forward together. United in solving problems, developing close site relationships and reaching the end goal. Operating as a key part of a global study team, the CRA plays a fundamental role in our clients’ drug development processes.

Planning and conducting various site visits (feasibility, site selection, interim and close-out) in accordance with the clinical monitoring plan. Full ownership of investigator sites for assigned studies with responsibility for the successful management of the site right through to close-out.

Dedicated, collaborative and inspire others.

Here at ICON we want our employees to succeed and ensure that they are set up for this success through constant training, development and support. To enable success in this position you will have:

• Prior experience of working in investigator site management, including conducting monitoring visits, from either a pharmaceutical company or a CRO environment.
• Prefer has submission experience before.
• A working knowledge of ICH-GCP guidelines and local and international regulatory requirements is essential.
• You will be educated to degree level, have equivalent experience or be a licensed healthcare professional.

Why ICON? Our focus is to provide you with a comprehensive and competitive total reward package that comprises, not only an excellent level of base pay, but also a wide range of variable pay and recognition programs. In addition, our best in class employee benefits, supportive policies and wellbeing initiatives are tailored to support you and your family at all stages of your career - both now, and into the future. Our success depends on the knowledge, capabilities and quality of our people. That’s why we are committed to developing our employees in a continuous learning culture – one where we challenge you with engaging work and where every experience adds to your professional development. ICON, including subsidiaries, is an equal opportunity and inclusive employer and is committed to providing a workplace free of discrimination and harassment. All qualified applicants will receive equal consideration for employment without regard to race, colour, 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. 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.

ICON and you

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To excel as a Clinical Research Associate (CRA) in a Clinical Research Organization (CRO), you need a combination of education, skills, and the right mindset. Brazil-based CRA II Debora shares her

Brazil-based CRA II Debora Oh shares her tips on how to become a great CRA and provides insight into life at ICON.

How to progress as a Clinical Research AssociateTo thrive as a Clinical Research Associate (CRA), it is imperative to cultivate a multifaceted skill set and demonstrate unwavering commitment to exce

 Senior CRA Yemi Moses recounts her development and shares her career ambitions with ICON plc.

Senior Clinical Research Associate Suzaita Hipolito talks about the satisfaction gained from working in Clinical Research. “What would it look like to wake up every day feeling happy and fulfilled?

Senior Clinical Research Associate, Suzaita Hipolito, talks about how working in Clinical Research gives her happiness and fulfilment.

Suzaita Hipolito

Press play to find out more

Similar jobs at ICON

Clinical Monitoring

Remote Working

Business Area

ICON Strategic Solutions

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Description

As Clinical Research Associate (CRA), you will be joining the world's largest & most comprehensive clinical research organization, powered by healthcare intelligence.  A CRA is a professional who cont

2023-103904

Expiry date

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

2024-109065

South Africa, Johannesburg

Johannesburg

Hybrid: Office/Remote

ICON Full Service & Corporate Support

Senior CRAClient Dedicated HomebasedICON plc is a world-leading healthcare intelligence and clinical research organisation. From molecule to medicine, we advance clinical research providing outsourced

Brazil, Sao Paulo

At ICON, it’s our people that set us apart. Our diverse teams enable us to become a better partner to our customers and help us to fulfil our mission to advance and improve patients’ lives. Our ‘Own I

Chile, Santiago

ICON plc is a world-leading healthcare intelligence and clinical research organization. From molecule to medicine, we advance clinical research providing outsourced services to pharmaceutical, biotech

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ISSCR announces Hong Kong, SAR as location for its 2025 Annual Meeting

The Global Stem Cell Event will be held 11-14 June 2025

International Society for Stem Cell Research

The world’s leading stem cell scientists will convene in Hong Kong, SAR, 11-14 June 2025 for the International Society for Stem Cell Research (ISSCR) 2025 Annual Meeting , illuminating the future of stem cell science and highlighting the most compelling research and clinical advances of the year.

Credit: ISSCR

The world’s leading stem cell scientists will convene in Hong Kong, SAR, 11-14 June 2025 for the International Society for Stem Cell Research (ISSCR) 2025 Annual Meeting , illuminating the future of stem cell science and highlighting the most compelling research and clinical advances of the year. The meeting is co-sponsored by The University of Hong Kong , The Chinese University of Hong Kong , and Hong Kong University of Science and Technology . The Hong Kong Innovation and Technology Commission and the Hong Kong Convention and Exhibition Centre provided significant support to enable the ISSCR to bring its hallmark event to the city of Hong Kong.

“We are honored to bring the ISSCR Annual Meeting to this region of the world for the first time since 2012 and appreciate the tremendous support of our co-sponsors to bring the meeting to Hong Kong,” Amander Clark, PhD, ISSCR President said. “It has been an incredible few years of basic discoveries and translational advances with stem cells, catapulting our field to the forefront of the most innovative science in the world. We look forward to celebrating the novel achievements of our global community in Hong Kong in 2025.”

For more than 20 years, the ISSCR Annual Meeting has convened bright minds in the stem cell field – to share knowledge, discovery, and diverse perspectives. The meeting represents the latest advances for the full breadth of our field, across multiple axes, including disciplines, geography, and cultures.

“The ISSCR 2025 Annual meeting in Hong Kong presents an unprecedent opportunity for fostering meeting of diverse minds from Asia, Oceania, the Americas and Europe that will inspire and engage stem cell researchers globally and seed international collaborations,” Kathy Cheah, Chair of the Hong Kong Bid Committee, said. “The impact will be huge!”

ISSCR 2025 will take place at the Hong Kong Convention and Exhibition Centre and is also supported by the   Hong Kong Tourism Board and the Croucher Foundation Limited .

Be among the first to see the program for ISSCR 2025 by signing up for alerts at ISSCR2025.org . Journalists who are interested in attending the meeting should email [email protected] .

About the International Society for Stem Cell Research ( www.isscr.org )  With nearly 5,000 members from more than 80 countries, the International Society for Stem Cell Research is the preeminent global, cross-disciplinary, science-based organization dedicated to stem cell research and its translation to the clinic. The ISSCR mission is to promote excellence in stem cell science and applications to human health. 

About Hong Kong Tourism Board The Hong Kong Tourism Board (HKTB) is a Government-subvented body.  Operating 15 offices around the world and representative offices in seven different markets, its primary mission is to maximize the social and economic contribution that tourism makes to the community of Hong Kong, and consolidate the city’s position as a world-class destination. The HKTB works closely with the Government, travel industry and other partners to promote Hong Kong worldwide, widen the range of tourism products and elevate service standards, as well as enhance the experiences of visitors during their stay.

Disclaimer: AAAS and EurekAlert! are not responsible for the accuracy of news releases posted to EurekAlert! by contributing institutions or for the use of any information through the EurekAlert system.

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Postdoctoral Fellow / Research Associate in gravitational lensing of dark matter substructures, Hong Kong

• by hyperspace_bot
• 2024/05/07 2024/05/07

The Department of Physics at CUHK, Hong Kong, invites applications for a Postdoctoral Fellow / Research Associate position in gravitational lensing of dark matter substructures.

We seek applicants with preferred expertise in strong gravitational lensing who want to expand their research focus to strong gravitational lensing involving gravitational waves. The ideal candidate will have considerable expertise in constructing lens models for galaxies as constrained by multiply-lensed light images, familiarity with analysing optical images, and will be committed to working with local experts to incorporate additional constraints provided by multiply-lensed gravitational-wave events. Current ground-based gravitational-wave detectors have the potential to reveal dark matter (DM) substructures through high-precision timing of the arrival of multiply-lensed gravitational waves. We envision that the combination of constraints from both light and gravitational waves will provide immunity from stellar microlensing and reveal the nature of such sub-structures.

At CUHK, since 2016, the group (led by Otto Hannuksela) has built tools to detect, analyse, and use gravitational-wave lensing with ground-based gravitational-wave detectors in isolation or with electromagnetic imaging (e.g., [1]). At HKU, the group (led by Jeremy Lim) is a leading expert in using traditional gravitational lensing of light rays to elucidate the nature of DM, including investigating the linkage between dark matter substructures and their model predictions, such as subhalos (e.g., WIMPs) and pervasive density modulations (e.g., Axions) (e.g., [2]). Furthermore, there are three dark matter groups (led by Kenny Ng, Tsang Keung Chan, Ming-Chung Chu) at CUHK that specialise in numerical simulations, indirect detection, and theory, and they have expertise in theoretical aspects of dark matter modelling.

Applicants should have (i) a PhD in Physics, Astronomy, or a related field and have a track record in lens modelling-expertise in implementing new strong lensing analyses and modelling, a publication track record in substructure lensing, and experience implementing Bayesian analysis models are highly advantageous.

The appointee will be responsible for filling the role of a lens modelling expert in the joint endeavour to connect these two branches of lensing and pursue dark matter studies. Apart from the joint work, the position comes with significant autonomy. The appointee is strongly encouraged to integrate and work with these groups freely and to develop his/her own independent research line throughout the study, with 50% time allotted to this purpose.

Appointment will be made on a contract basis for two years commencing September 2024, renewable, subject to mutual agreement. Applications will be reviewed immediately and continue until the position is filled.

Application Instructions Applicants should submit the following documents in the online application: (1) an up-to-date CV; (2) a cover letter; (3) the names and contact information of at least two referees; (4) a research statement outlining his/her interests and qualifications; and (5) two reference letters. Please submit these to the link given in the URL

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