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Clinical Trials Jobs in Vijayawada

1 - 13 of 13
1 - 13 of 13
Search Results - Clinical Trials Jobs in Vijayawada
apartmentTWO95 International, IncplaceVijayawadaevent_available
and reporting in clinical trials  •  Proficient in SAS and R for statistical modelling, efficacy analysis, and data interpretation  •  Ability to collaborate closely with programming and clinical teams in an agile setup....
apartmentEphicacyplaceVijayawadaevent_available
Description -  •  Develop, validate, and maintain SDTM/ADaM datasets, TLFs (Tables, Listings & Figures) and submission-ready outputs.  •  Perform end-to-end statistical programming activities across all phases of Oncology clinical trials.  •  Support...
apartmentCytelplaceVijayawadaevent_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...
apartmentCloudLabs IncplaceVijayawadaevent_available
strategic initiatives supporting the Global Clinical IT team. In this role, the individual will be a technical developer to support business initiatives within Medidata Rave suites of applications. This individual should have demonstrated prior experience...
apartmentCytelplaceVijayawadaevent_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...
apartmentK3-Innovations, Inc.placeVijayawadaevent_available
Job Title: Clinical Quality Compliance Manager Location: Bengaluru, Karnataka, India Reports To: QA/Compliance Director or Clinical Operations Director Job Summary: Clinical Site Auditor to ensure compliance and quality at Clinical Trial sites...
apartmentAstekplaceVijayawadaevent_available
Key Responsibilities  •  Develop, validate, and maintain ADaM datasets, TLFs, and other analytical outputs for clinical trials.  •  Support Oncology studies by ensuring accuracy, consistency, and regulatory compliance in all programming deliverables...
apartmentprinceps technologiesplaceVijayawadaevent_available
requires strong technical proficiency, autonomy, and the ability to collaborate effectively within cross-functional and global teams. Core Responsibilities  •  Program, validate, and maintain clinical trial datasets and outputs using SAS and R.  •  Lead...
apartmentQinecsa SolutionsplaceVijayawadaevent_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...
apartmentSUN PHARMAplaceVijayawadaevent_available
experience in processing clinical trial data in the biotechnology, pharmaceutical, CRO or health care related industry.  •  Oncology Therapeutic area preferred.  •  Strong SAS programming skills in a clinical data environment with excellent analytical skills...
apartmentExcelraplaceVijayawadaevent_available
Good understanding of current best practices in computational biology data-management (NGS/Transcriptiomics/Microarray/Proteomics/Clinical-trials/Text-mining, etc.).  •  Expertise in one or more programming/scripting languages such as R, Python, shell...
apartmentStoryline HealthplaceVijayawadaevent_available
troops.  •  Homeless organizations identifying people who can be helped off the street.  •  Discovering new end points for clinical trials  •  Oncologists predicting drug timing for cancer patients.  •  Predicting treatment responses for psychiatry patients...
apartmentHealthifyplaceVijayawadaevent_available
Managing/Moderating group coaching on chat groups by motivating clients toward fitness.  •  Converting free trial clients to premium clients.  •  Passionate about communication and cracking the revenue targets assigned each month.  •  Strong commitment of 8-9hrs...

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