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Clinical Trials Jobs in Nagpur

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Search Results - Clinical Trials Jobs in Nagpur
apartmentQuantum IntegratorsplaceNagpurevent_available
established processes and guidelines to ensure consistency and audit readiness. Required Skills & Experience:  •  Bachelor’s degree in Life Sciences, Clinical Research, Biotechnology, or related field  •  3-5 years of experience in clinical trials, clinical data...
apartmentSignant HealthplaceNagpurevent_available
About Signant Health At Signant Health, we help bring life-changing treatments to patients faster. We are a global evidence generation company that supports clinical trials with smart technology, scientific expertise, and hands-on operational...
apartmentDizzarooplaceNagpurevent_available
trial data flow, data cleaning, query management, and documentation. In addition to traditional clinical data management responsibilities, this person should be open to learning and using AI tools to improve productivity, automate repetitive tasks...
apartmentQuantum IntegratorsplaceNagpurevent_available
to ensure consistency and audit readiness. Required Skills & Experience: Bachelor’s degree in Life Sciences, Clinical Research, Biotechnology, or related field 1–2 years of experience in clinical trials, clinical data review, or system testing/UAT Basic...
apartmentSIROplaceNagpurevent_available
Key Accountabilities:  •  Create eCRF specifications, design, develop and unit test and functionally validate clinical trial setup process  •  Create edit check specifications and program or modify checks at study level within EDC  •  Setup different...
apartmentMSD MalaysiaplaceNagpurlanguageappcast.ioevent_available
Regulatory compliance to import products for clinical trials & CDTL testing.* Providing requested documents for registration of products in Export markets & approving all artworks & other requisites on timely basis.* Approval of artworks on imported & local...
apartmentprinceps technologiesplaceNagpurevent_available
Job Title: Senior Statistical Programmer (Oncology) Location: Canada/IN Employment Type: Full-Time Experience: 8+ Overview We are seeking an experienced Senior Statistical Programmer with strong Oncology clinical trial experience to support end...
apartmentCosMicIT ?? ?? ?? ??placeNagpurevent_available
/libraries or creates new ones to support the review of clinical trial data and trial status information for cross-functional use and provides input on data management reporting standards as required  •  Ensure accurate delivery by creating macros for Standard...
apartmentValos SrlplaceNagpurevent_available
Responsibilities  •  Create ADAM and TFLs for clinical studies  •  Apply advanced statistical methodologies to clinical trials and RWE studies  •  Contribute to the development of Statistical Analysis Plans (SAPs) and study reports  •  Collaborate closely with cross...
apartmentMedpaceplaceNagpurlanguagemncjobsindia.comevent_available
certification preferred 1-3 years of experience in clinical research or imaging related field and at least 2 years of experience as an Imaging Technologist in a hospital or imaging center and Experience working with clinical trials or within...
apartmentCytelplaceNagpurevent_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...
apartmentCytelplaceNagpurevent_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...
apartmentIQVIA IndiaplaceNagpurevent_available
and oversight of centralized monitoring activities to ensure subject safety, data integrity, regulatory compliance, and delivery of clinical trial objectives as per sponsor and contract requirements. The role partners with clinical, project, analytics, quality...
apartmentQinecsa SolutionsplaceNagpurevent_available
Registration Experience: 1 - 3 years in Pharmacovigilance Primary Responsibilities As a medical reviewer  •  Conduct review and assessment of individual case safety reports obtained from clinical trials, spontaneous and solicited reports  •  Determine...
apartmentImaging EndpointsplaceNagpurevent_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...
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