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Clinical Trials Jobs in Hyderabad

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Search Results - Clinical Trials Jobs in Hyderabad
apartmentConnexRplaceHyderabadevent_available
that support clinical research, treatment outcomes, and healthcare decision-making. The ideal candidate should have experience working with clinical trials, EHR, claims data, and real-world evidence (RWE) and be skilled in statistical analysis, machine learning...
apartmentImaging EndpointsplaceHyderabadevent_available
that are passionate in their desire to assist us in our mission to customize each clinical trial’s imaging to optimize the opportunity to demonstrate efficacy. Imaging Endpoints is based in Scottsdale, Arizona, with offices in Cambridge, Massachusetts; London, UK...
apartmentLatinum HR SolutionsplaceHyderabadevent_available
are looking for an experienced Statistical Programmer to oversee programming activities for clinical trials, regulatory submissions, and integrated analyses. This role involves leading a team, ensuring high-quality deliverables, and developing efficient...
apartmentW3GlobalplaceHyderabadevent_available
of clinical trials, FDA regulations, and industry terminology  •  Experience hiring for roles such as Scientist, Chemist, Research Associate, Biologist, MD, Nurse, Clinical Project Manager, Regulatory Associate, Medical Writer, etc.  •  Proficiency with ATS...
apartmentNovartisplaceHyderabadlanguagemncjobsindia.comevent_available
Skills Clinical Study Reports Data Analysis Documentation Management Lifesciences Operational Excellence Regulatory Compliance Languages English Skills Desired Clinical Study Reports Data Analysis Documentation Management Lifesciences...
apartmentKPI PartnersplaceHyderabadevent_available
Clinical trials experience, SDTM knowledge, SAS programming SAS programmer with SDTM knowledge, migration of the oncology studies SQL Knowledge is prefered...
apartmentOcugen India Pvt LtdplaceHyderabadevent_available
Job title Lead Statistical Programmer Reports to VP- Operations Job purpose To lead the programming, validation, and delivery of high-quality statistical outputs for clinical trials by applying advanced SAS programming and CDISC standards...
apartmentCytelplaceHyderabadevent_available
As a Senior Statistical Programmer, you will leverage your advanced SAS programming skills and proficiency in CDISC standards (SDTM & ADaM) to support or lead one or more Phase I-IV clinical trials. This role can be performed as fully remote. Our values  •  We...
apartmentImaging EndpointsplaceHyderabadevent_available
that are passionate in their desire to assist us in our mission to customize each clinical trial's imaging to optimize the opportunity to demonstrate efficacy. Imaging Endpoints is based in Scottsdale, Arizona, with offices in Cambridge, Massachusetts; London, UK...
apartmentCytelplaceHyderabadevent_available
that data summaries are delivered in a consistent, high-quality manner. This individual will be responsible for implementing all reporting and analysis activities for the Sponsor clinical trials. Responsibilities As a Principal Statistical Programmer, your...
apartmentAccentureplaceHyderabadlanguageaccenture.comevent_available
laboratories, clinical trials support, and regulatory services, to pharmacovigilance and patient services solutions. Employees under this span will be a part of one of the sub-offerings - Clinical, Pharmacovigilance & Regulatory, helping the world’s leading...
apartmentRose InternationalplaceHyderabadevent_available
research, healthcare, and life sciences roles (e.g., Clinical Research Associates, Clinical Data Managers, Regulatory Affairs Specialists, Clinical Trial Assistants, Pharmacovigilance Associates, etc.).  •  Use niche clinical sourcing platforms...
apartmentBristol Myers SquibbplaceHyderabadlanguagefoundit.inevent_available
will report into a line manager within Global Trial Management. The GTA can potentially support any therapeutic areas and research phase and will collaborate with cross-functional global teams to execute assigned operational aspects of global clinical research...
apartmentPlanet PharmaplaceHyderabadevent_available
Contribute to ongoing study decisions and strategic planning during a critical period ahead of the data lock. Must‑Have Experience Extensive hands-on experience as a Statistician supporting multiple late‑stage clinical trials simultaneously. Proven ability...
apartmentAurigene Pharmaceutical Services LimitedplaceHyderabadevent_available
excipients and specialized packaging components with SCM.3. Project Execution, Monitoring & ControlTimeline & Cost Tracking: Rigorous monitoring of the Gantt chart, focusing on critical path items like Stability data time-points and Clinical Trial Material...
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