(Senior) Clinical Research Associate
3 days ago
(Senior) Clinical Research Associate (CRA) Job Overview Perform monitoring and site management work to ensure that sites are conducting the study(ies) and reporting study data as required by the study protocol, applicable regulations and guidelines, and sponsor requirements. Essential Functions Perform site monitoring visits (selection, initiation, monitoring and close‑out visits) in accordance with contracted scope of work and regulatory requirements, i.e., Good Clinical Practice (GCP) and International Conference on Harmonization (ICH) guidelines Work with sites to adapt, drive, and track subject recruitment plan in line with project needs to enhance predictability. Administer protocol and related study training to assigned sites and establish regular lines of communication with sites to manage ongoing project expectations and issues. Evaluate the quality and integrity of study site practices related to the proper conduct of the protocol and adherence to applicable regulations. Escalate quality issues as appropriate. Manage the progress of assigned studies by tracking regulatory submissions and approvals, recruitment and enrollment, case report form (CRF) completion and submission, and data query generation and resolution. May support start‑up phase. Ensure copies/originals (as required) site documents are available for filing in the Trial Master File (TMF) and verify that the Investigator's Site File (ISF) is maintained in accordance with GCP and local regulatory requirements. Create and maintain appropriate documentation regarding site management, monitoring visit findings and action plans by submitting regular visit reports, generating follow‑up letters and other required study documentation. Collaborate and liaise with study team members for project execution support as appropriate. If applicable, may be accountable for supporting development of project subject recruitment plan on a per site basis. If applicable, may be accountable for site financial management according to executed clinical trial agreement and retrieve invoices according to local requirement. Qualifications Bachelor's Degree in scientific discipline or health care preferred. Req Requires at least 1 year of on-site monitoring experience. Req Equivalent combination of education, training and experience may be accepted in lieu of degree. Req Good knowledge of, and skill in applying, applicable clinical research regulatory requirements (i.e., Good Clinical Practice (GCP) and International Conference on Harmonization (ICH) guidelines). Good therapeutic and protocol knowledge as provided in company training. Computer skills including proficiency in use of Microsoft Word, Excel and PowerPoint and use of a laptop computer and iPhone and iPad (where applicable). Written and verbal communication skills including good command of English language. Organizational and problem-solving skills. Effective time and financial management skills. Ability to establish and maintain effective working relationships with coworkers, managers, and clients. 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 #J-18808-Ljbffr
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Hong Kong Island, Hong Kong SAR China ICON Strategic Solutions Full timeCRA II/ Senior CRA - office-based in Hong Kong. Join us and advance your career with an industry leading CRO. 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 on our mission to shape the future of clinical...
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Clinical Trials Support Assistant
3 days ago
Hong Kong Island, Hong Kong SAR China Hong Kong Center For Clinical Research Limited Full timeA clinical research center in Hong Kong is looking for a candidate to support daily operations and administrative work related to clinical trials. Responsibilities include data entry, processing study specimens, and participating in outreach activities for recruitment. An Associate Degree in Science or Pharmacy is required, along with strong English and...
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Hong Kong Island, Hong Kong SAR China ICON Strategic Solutions Full timeA leading clinical research organization is seeking a Senior Clinical Research Associate in Hong Kong. In this role, you will oversee clinical trial activities ensuring compliance with protocols and regulatory standards. The ideal candidate should have an advanced degree in life sciences and extensive CRA experience. ICON offers competitive salary and a...
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Clinical Research Associate
1 day ago
Hong Kong Island, Hong Kong SAR China Tigermed Full timeJob Purpose This position is responsible for project management and study site management from site selection to initiation until monitoring and close‑out of assigned clinical study studies in accordance with Tigermed or sponsor Standard Operating Procedures (SOPs), International Conference on Harmonization Good Clinical Practice standard (ICH‑GCP),...
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Hong Kong Island, Hong Kong SAR China Fortrea Hong Kong Limited Full timeA clinical research organization in Hong Kong is seeking a Clinical Research Associate to manage clinical studies and ensure compliance with ICH GCP Guidelines. The role requires 1+ years of Clinical Monitoring experience and fluency in both Cantonese/Mandarin and English. Responsibilities include site monitoring, data integrity verification, and preparing...
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Clinical Research Associate
1 week ago
hong kong, Hong Kong SAR China Tigermed Full timeInternational Business Unit Functional Support Job Purpose This position is responsible for project management and study site management from site selection to initiation until monitoring and close-out of assigned clinical study studies in accordance with Tigermed or sponsor Standard Operating Procedures (SOPs), International Conference on Harmonization Good...
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Research Assistant
3 days ago
Hong Kong Island, Hong Kong SAR China Hong Kong Center For Clinical Research Limited Full timeSupport clinical center's daily operation Support administrative work to support clinical trials conduct - including but not limited to documents preparation and archival, data entry Process study specimens Have opportunities to coordinate minor projects Ensure high quality of work meeting Good Clinical Practice (GCP) and other applicable regulatory...
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Hong Kong Island, Hong Kong SAR China Tigermed Full timeA clinical research organization in Hong Kong is seeking an Associate for project management and site management of clinical studies. Responsibilities include site selection, training site staff, ensuring compliance with regulations, and managing budgets. Ideal candidates should have a Bachelor's degree in a related field and at least one year of experience...
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Clinical Research Associate
3 days ago
Hong Kong Island, Hong Kong SAR China Fortrea Full timeFortrea is excited to connect with talented individuals for future opportunities. If you meet the job requirements, we'll invite you for an interview. If you're pre-selected, our recruiter will keep in touch and let you know when the role officially opens, so we can reconfirm your interest before moving forward with an offer. Responsibilities Site management...
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Hong Kong Island, Hong Kong SAR China THE UNIVERSITY OF HONG KONG Full timeA prestigious educational institution in Hong Kong seeks exceptional candidates for the position of Tenure-Track Clinical Associate Professor in the LKS Faculty of Medicine. The role emphasizes strong clinical skills, teaching experience, and a commitment to research. Successful applicants will engage in undergraduate and postgraduate education while...
