Save Job Back to Search Job Description Summary Similar JobsExcellent opportunity in MNCComprehensive training and professional developmentAbout Our ClientOur client is well-established medical company, they are looking for a high calibre to join the team as Senior Clinical Research Assistant to oversee and ensure compliance with clinical trials. This role involves monitoring adherence to protocols, SOPs, GCP, and regulatory requirements.Job DescriptionOversee clinical trial progress and ensure compliance with protocols and regulationsDevelop and maintain relationships with clinical investigators, CROs, hospitals, and research institutionsReview adverse event cases, manage budgets and schedules, and prepare study documents and status reportsAssist in the design, development, and monitoring of clinical evaluation projectsTrain investigators and site personnelImplement clinical development strategies and assist in recommending qualified investigatorsEnsure effective recruitment and retention of patientsThe Successful ApplicantMinimum of 4 years of clinical research experience, on-site monitoring in a pharmaceutical, biotech or CRO environmentBachelor's Degree Degree in scientific discipline or health care preferredStrong knowledge of clinical trial management and adherence to GCP and regulatory standardsIndependent, Hands-on, adaptable, with excellent stakeholder management and communication skillsProficient in Cantonese, Mandarin and EnglishWhat's on OfferThis company offers the successful candidates an attractive salary package with bonus and benefits.ContactZalika HoQuote job refJN-052023-6048261Phone number+852 2848 4783Job summaryFunctionLife SciencesSpecialisationMedical devicesIndustryHealthcare / PharmaceuticalLocationHong KongJob Type:PermanentConsultant nameZalika HoConsultant phone+852 2848 4783Job ReferenceJN-052023-6048261
