Save Job Back to Search Job Description Summary Similar JobsLead global clinical trials from start-up to close-outShape strategy in high-priority, high-impact studiesAbout Our ClientOur client is a globally respected organization known for its commitment to innovation, scientific excellence, and patient-focused solutions. Operating across numerous therapeutic areas, they support complex clinical programs that advance modern healthcare. With a collaborative culture and a strong emphasis on compliance, continuous learning, and employee empowerment, this is an environment where you can build a meaningful career while contributing to global clinical development goals.Job DescriptionLead site start-up activities including regulatory document managementCustomize and negotiate informed consent forms in alignment with local regulationsServe as liaison with ethics committees and competent authoritiesManage site contracts and negotiate study budgetsMonitor and ensure site compliance with required trainingTrack and enforce study timelines aligned with organizational goalsMaintain active collaboration with sites during all study phasesCommunicate effectively with internal and external stakeholders to drive study progressEnsure all regulatory and data privacy requirements are metIdentify and resolve site-level operational issues, escalating when necessaryOversee delivery of clinical trial materials for site activationManage translation workflows and ensure document qualityAccurately maintain internal systems and document repositoriesAct as a senior contributor on high-priority and complex studiesProvide oversight, coaching, and support to junior team membersThe Successful ApplicantSignificant experience in clinical operations or trial start-up rolesDeep understanding of global and country-specific regulatory requirementsStrong experience managing complex or large-scale multi-site trialsSkilled in contract negotiation and budget discussionsExcellent interpersonal and stakeholder management abilitiesHighly organized with a focus on compliance and documentation accuracyAbility to lead timelines across multiple functional teamsComfortable supporting or mentoring more junior colleaguesProficient in trial systems and documentation platformsFluent in English; other languages beneficialWhat's on OfferGlobal reach and real responsibility in study deliveryOpportunity to lead and shape high-profile clinical programsContactIvy ChiQuote job refJN-052025-6742489Phone number+886287298212Job summaryJob functionLife SciencesSpecialisationClinical OperationsWhat is your area of specialisation?Healthcare / PharmaceuticalLocationTaipei CityContract TypePermanentConsultant nameIvy ChiConsultant phone+886287298212Job ReferenceJN-052025-6742489
