Study Start-up Cra

This role will be key to ensure strong monitoring in our clinical trials. Under the oversight of the CRD or Head of Site Management and Monitoring, the person is responsible to manage a team of 6-14 CRAs and to ensure excellent study and site performance with strict adherence to local regulations, company SOPs and ICH GCP. As line manager the role is...

As a Senior Clinical Research Associate you will be joining the world's largest & most comprehensive clinical research organisation, powered by healthcare intelligence.You will be partnering with one of our global pharmaceutical clients; a science-based company with one of the most exciting product pipelines in the industry. This global pharmaceutical client...

The Regional Study Coordinator (RSC) is responsible for the successful delivery of all operations of a clinical study in their specific area of the world. The RSC acts as the appointed Liaison between Global Project Management, Client Representatives and other CCLS departments involved in the clinical study to ensure the successful management of regional...

Responsibilities: Lead site identification and site selection activities. Lead set up of clinical components in CTMS Prepare for and attend investigator meetings; may present materials. Develop and distribute Clinical Monitorring Plan (CMP) and update as required Develop and distribute Site Initiation Visit (SIV) materials. Develop and distribute Source Data...

Role SummaryThe study director represents the single point of study control with the ultimate responsibility for the overall scientific conduct of the study, from the conceptualization to the closure. Study director plans, sets up and manages in vitro/vivo studies in a cross-functional way and in accordance with regulatory guidelines; interprets robust data...

Role SummaryThe study director represents the single point of study control with the ultimate responsibility for the overall scientific conduct of the study, from the conceptualization to the closure. Study director plans, sets up and manages in vitro/vivo studies in a cross-functional way and in accordance with regulatory guidelines; interprets robust data...

Roles & ResponsibilitiesRole Summary This role represents the single point of study control with the ultimate responsibility for the overall scientific conduct of the study, from conceptualization to closure Plans, sets up and manages in vitro/vivo studies in a cross-functional way and in accordance with regulatory guidelines, interprets robust data up to...

As our business grows, we are looking to further strengthen our Clinical Operations team in IQVIA Pakistan. We have a number of great opportunities for Clinical Research Associate and Senior Clinical Research Associate in Karachi, Lahore, and Islamabad.You will perform monitoring and site management work to ensure that sites are conducting the study(ies) and...

Company10x Study AcademyDesignationTikTok / IG InternDate Listed03 Jun 2024Job TypeEntry Level / Junior Executive Full/PermPart/TempIntern/TSJob PeriodImmediate Start, For At Least 2 MonthsProfessionOthers / General WorkIndustryEarly Childhood Care and EducationLocation NameSingaporeAllowance / Remuneration$500 - 1,500 monthlyCompany ProfileWe are an...

PPD's mission is to improve health. It starts as an idea to find a cure. It becomes a life saved. All in-between, it's you We know that meaningful results not only require the right approach, but also the right people. We invite you to re-imagine health promoting protocols with us, working alongside our talented, bright and energetic teams.Our global...

Roles & ResponsibilitiesInterested applicants are invited to apply directly at the NUS Career Portal.Your application will be processed only if you apply via NUS Career Portal.We regret that only shortlisted candidates will be notified.Job DescriptionThe Department of Chinese Studies, National University of Singapore (NUS), is one of the leading institutions...

Contract type: Contractual role 6 monthsLocation: SingaporeJOB OVERVIEWStudy Group is seeking a highly motivated, bright, dynamic, and adaptable individual contributor who thrives in an innovative, performance-oriented environment. Applicants should have a mindset of continuous improvement and change and demonstrate curiosity, collaboration, and the ability...

Responsibilities / Duties:In this role you will be responsible for managing clinical projects to ensure the successful delivery of all lab services, including kits shipment, sample testing and sample management of a clinical study for the Asia regionAct as regional liaison between Labcorp Central Lab Services (CLS) Global Study Manager and various CLS...

Responsibilities / Duties:In this role you will be responsible for managing clinical projects to ensure the successful delivery of all lab services, including kits shipment, sample testing and sample management of a clinical study for the Asia regionAct as regional liaison between Labcorp Central Lab Services (CLS) Global Study Manager and various CLS...

Responsibilities / Duties:In this role you will be responsible for managing clinical projects to ensure the successful delivery of all lab services, including kits shipment, sample testing and sample management of a clinical study for the Asia regionAct as regional liaison between Labcorp Central Lab Services (CLS) Global Study Manager and various CLS...

Manage assigned clinical trials by scheduling, reviewing, and driving project tasks and deliverables within a clinical team and cross-functional team leads. Prepare and review project status reports to ensure timely completion of project objectives in compliance with all regulations and SOPs. Follow up on projectspecific deliverables across the team and...

Identify, select, initiate, and close-out appropriate investigational sites for clinical studies. Monitor those sites in order to ensure that studies are carried out according to the study protocol, ICON SOPs/WPs, applicable regulations and the principles of ICH-GCP Depending upon experience, become involved, when required, in other areas of study management...

Under the direct responsibility of the Executive Director, the Director of Studies is responsible for the Language Centre's activities:Language Centre management: manage and oversee the work of the teaching and administrative staff of the Language Centre (25 teachers, 3 classroom assistants, 1 registrar, 3 registration officers, 1 academic coordinator)...

Roles & ResponsibilitiesJob DescriptionSupport the investigators in implementing clinical trials protocols: Liaise with the study site personal to implement the study per global and local requirements. Ensure compliance with all ethical, regulatory and contractual requirements. Training of study site personal (protocol, use of IP, SOPs, etc.). Ensuring data...

Roles & ResponsibilitiesResponsibilities: Support the investigators in implementing clinical trials protocols Liaise with the study site personal to implement the study per global and local requirements Ensure compliance with all ethical, regulatory and contractual requirements. Training of study site personal (protocol, use of IP, SOPs, etc.).>...