Associate Clinical Trial Leader
2 days ago
Your responsibilities include, but are not limited to:May lead studies in maintenance or in closeout phase or ongoing studies post primary database lock with the oversight of the LCTL/CTL, as assigned. Support the clinical protocol development process in collaboration with the CTL/Lead CTL and the Clinical program Leader (CPL): chip in to the development of clinical protocols, amendments and related documents; drive and/or supprt trial-related documents and processes.development of clinical section of regulatory documents like Investigator’s Brochure, safety updates, IND/NDA submission documents, responses to Health Authorities questions.support the global multidisciplinary CTT to ensure all trial results are met according to timelines, budget, quality standards and operational procedures: attend CTT meetings, assist in report study progress and issues.support the CTL/Lead CTL, in the ongoing review and cleaning of the clinical trial data, support final analysis and interpretation including the development of clinical trial reports, publications and internal/external presentations.coordinate the real time availability of quality clinical trial data, including safety, efficacy, pharmacokinetic, imaging and biomarker data, to provide consolidated information for dose escalation meetings with investigators.Responsible for accuracy of trial information in all trial databases and tracking systems. Attend relevant meetings to support ongoing execution of clinical trial and program level activities.ensure that program specific standards/activities (e.g., CRFs, UAT testing, database specifications, Data Handling plan, outsourcing specifications including imaging, biomarkers, PK, data monitoring, validation plans and data transfer specifications) are applied to the clinical trial, where applicable.develop clinical outsourcing specifications to facilitate bid templates and selection of CROs and other 3rd parties including central lab and imaging vendors; handle work with external vendors in collaboration with the CRO; Management Department as well as with the Assay Research Lab. This also includes the set-up, logistics, documentation and clinical supplies needed for the clinical trial(s).
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hyderabad, India Imaging Endpoints Full timeSUMMARYImaging Endpoints (IE) is an Imaging Technology and Imaging Clinical Research Organization (iCRO). We are passionately focused on our vision to Connect Imaging to the Cure™. Everything we do is aligned with this singular purpose. We work every day excited to advance imaging science, technology, and services to bring curative technologies to...
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Hyderabad, India Imaging Endpoints Full timeSUMMARY Imaging Endpoints (IE) is an Imaging Technology and Imaging Clinical Research Organization (iCRO). We are passionately focused on our vision to Connect Imaging to the Cure™. Everything we do is aligned with this singular purpose. We work every day excited to advance imaging science, technology, and services to bring curative technologies to...
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Hyderabad, India Whatjobs IN C2 Full timeSUMMARY Imaging Endpoints (IE) is an Imaging Technology and Imaging Clinical Research Organization (iCRO). We are passionately focused on our vision to Connect Imaging to the Cure™. Everything we do is aligned with this singular purpose. We work every day excited to advance imaging science, technology, and services to bring curative technologies to...
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Clinical Trial Supply Manager
7 days ago
Hyderabad (Office), India Novartis Full time ₹ 12,00,000 - ₹ 36,00,000 per yearBandLevel 4Job Description SummaryGCS Clinical Trial Supply Manager (CTSM) defines and executes an optimal clinical trial supply strategy for a clinical trial including effective risk management to ensure supply continuity to patients. The CTSM is the GCS single point of contact at trial level for the integrated Clinical Trial Team (iCTT). Is responsible for...
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Clinical Trial Administrator
2 weeks ago
Hyderabad, Telangana, India Biological E Full time ₹ 9,00,000 - ₹ 12,00,000 per yearRole & responsibilitiesAssist with the Ethics / Regulatory Submissions; keep a track of submissions & approvals for the study.Help medical team in preparing Protocols, Investigator Brochures and CRFs which includes keeping track and re-ordering supplies.Set up and maintenance of the Trial Master Files (TMF) or Electronic filing systems/ set up of the...
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Hyderabad, India Imaging Endpoints Full timeSUMMARYImaging Endpoints (IE) is an Imaging Technology and Imaging Clinical Research Organization (i CRO). We are passionately focused on our vision to Connect Imaging to the Cure™. Everything we do is aligned with this singular purpose. We work every day excited to advance imaging science, technology, and services to bring curative technologies to...
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Hyderabad, India Imaging Endpoints Full timeSUMMARYImaging Endpoints (IE) is an Imaging Technology and Imaging Clinical Research Organization (iCRO). We are passionately focused on our vision to Connect Imaging to the Cure™. Everything we do is aligned with this singular purpose. We work every day excited to advance imaging science, technology, and services to bring curative technologies to...
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Hyderabad, India Imaging Endpoints Full timeJob Description SUMMARY Imaging Endpoints (IE) is an Imaging Technology and Imaging Clinical Research Organization (iCRO). We are passionately focused on our vision to Connect Imaging to the Cure. Everything we do is aligned with this singular purpose. We work every day excited to advance imaging science, technology, and services to bring curative...
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hyderabad district, India Imaging Endpoints Full timeSUMMARY Imaging Endpoints (IE) is an Imaging Technology and Imaging Clinical Research Organization (iCRO). We are passionately focused on our vision to Connect Imaging to the Cure™. Everything we do is aligned with this singular purpose. We work every day excited to advance imaging science, technology, and services to bring curative technologies to...
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Clinical Trial Registration Specialist
5 days ago
Hyderabad, Telangana, India Bristol Myers Squibb Full time ₹ 12,00,000 - ₹ 24,00,000 per yearWorking with UsChallenging. Meaningful. Life-changing. Those aren't words that are usually associated with a job. But working at Bristol Myers Squibb is anything but usual. Here, uniquely interesting work happens every day, in every department. From optimizing a production line to the latest breakthroughs in cell therapy, this is work that transforms the...
