Clinical Research Associate II
5 days ago
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 #J-18808-Ljbffr
-
WorkFromHome, Hong Kong SAR China Emerald Clinical Full timeA global Contract Research Organization is seeking a highly organized Project Specialist to join their Early Phase Project Management team in Hong Kong. The role involves supporting project managers in delivering global clinical trials, maintaining project documentation, and coordinating meetings. Candidates should possess a relevant bachelor's degree and...
-
WorkFromHome, Hong Kong SAR China Emerald Clinical Full timeA leading Contract Research Organization in Hong Kong is seeking a proactive Project Specialist to support clinical trials. This full-time role involves managing documentation, coordinating meetings, and ensuring timelines are met. Ideal candidates have a Bachelor's degree in Life Sciences and 2–3 years of clinical research experience. Competitive...
-
Project Specialist, Asia
2 weeks ago
WorkFromHome, Hong Kong SAR China Emerald Clinical Full timeJoin to apply for the Project Specialist, Asia role at Emerald Clinical 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,...
-
Project Specialist, Asia
5 days ago
WorkFromHome, Hong Kong SAR China Emerald Clinical Full timeAt 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...
-
Renal Franchise Strategy Lead
7 days ago
WorkFromHome, Hong Kong SAR China Emerald Clinical Full timeA global Contract Research Organization is looking for a Therapeutic Franchise Head (Renal) in Hong Kong. This role requires extensive experience in clinical research and business development. The successful candidate will develop delivery strategies, collaborate with experts, and act as the project champion for awarded projects. This position offers...
-
Therapeutic Franchise Head
7 days ago
WorkFromHome, Hong Kong SAR China Emerald Clinical Full timeWe are Emerald Clinical Trials , a global, full‑service Contract Research Organization (CRO) with a strong heritage in the Asia‑Pacific region. We advance clinical research by combining scientific expertise with operational excellence across all trial phases, from registration to post‑marketing. About the Role The Therapeutic Franchise Head (Renal) is...
-
Senior CRA II: Global Site Monitoring
5 days ago
WorkFromHome, Hong Kong SAR China ICON Full timeA leading clinical research organization in Hong Kong seeks an experienced Clinical Research Associate to monitor clinical trial sites and ensure adherence to study protocols and regulatory requirements. The role demands excellent organizational and communication skills, alongside a strong understanding of clinical trials. You will be responsible for...
-
Hybrid Genetic Counsellor: Clinical, Training
2 weeks ago
WorkFromHome, Hong Kong SAR China Genetic Counselling Asia Full timeA genetic counselling organization in Hong Kong is seeking a Genetic Counsellor for a hybrid role. This role involves conducting intake and genetic counselling for clients, supporting medical professionals with genetic testing recommendations, and engaging in clinical research. Qualified candidates should have a Master's in Genetic Counselling, relevant...
-
External Title Clinical Trial Manager
5 days ago
WorkFromHome, Hong Kong SAR China Medpace Hong Kong Limited Full timeMedpace Clinical Trial Manager – Infectious Disease Medpace is a scientifically led organization offering full-service solutions for our clients, giving the Medpace project teams the empowerment to truly lead and execute clinical trials. The Clinical Trial Manager position is the lead role for multiservice global/regional clinical trials. The CTM interacts...
-
Research Compliance Associate
5 days ago
WorkFromHome, Hong Kong SAR China Avomind Full timeThe Company Our client is the global leader in knowledge on-demand. They connect investors and business leaders with the knowledge they need to succeed. Working from nine cities globally, their 1500+ colleagues provide round-the-clock coverage to the world's top investment funds, consultancies, and businesses. Founded in 2008, our client is a fast-growing,...