Clinical Trials Systems Administrator
7 days ago
System Support ProfessionalServe as a technical authority for diagnosing and resolving complex system issues, performance bottlenecks, and data integrity problems. Utilize exceptional analytical and diagnostic skills with a methodical approach to root cause analysis and complex problem-solving.**Required Qualifications:**8+ years of working experience with a minimum of one or more years implementing systems in the clinical research/trials domain.Knowledge of ITIL frameworks (ITIL Foundation certification is a plus)Demonstrated excellent verbal and written communication skills.Contribute to the continuous improvement of support processes, tools, and automation initiatives.System Support and Customer-facing experience**Benefits Include:**Flexibility to work in extended shift and night shifts (rotational)Opportunity to collaborate with cross-functional teams including development, infrastructure, and business analysts.**Key Skills:Strong command of SQL, Unix/Linux and Windows environments and ITIL processes.Scripting experience (any one - Python or Ruby preferred)Writing SQL queriesKnowledge of Ruby programming is desirable. Knowledge of clinical trials related standards and GxP practices is desirable.**Job Summary:** This role requires excellent communication skills and a good understanding of the clinical trials domain. The ability to troubleshoot and resolve client-specific technical cases, assist with escalation of cases from level one & two support staff, assist with client projects moving from project to production environment, and training of clients & staff. This is a fast-paced role, requiring flexibility working with several different stakeholders while being exposed to a variety of technologies and environments.
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Lead Stat Programmer Clinical Trials
2 weeks ago
visakhapatnam, India beBeeStatisticalProgramming Full timeJob DescriptionWe are seeking an experienced Statistical Programming Lead to lead one or more Phase I-IV studies programming activities as per the project strategies. This role requires strong SAS programming skills, excellent analytical skills and a good understanding of pharmaceutical clinical development principles.Lead statistical programming activities...
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Clinical Site Compliance Specialist
2 weeks ago
visakhapatnam, India beBeeClinicalAuditor Full timeClinical Research Site AuditsWe are seeking a Clinical Site Auditor to ensure compliance and quality at clinical trial sites. The ideal candidate will conduct site audits, review documentation, and verify adherence to protocols, GCP, GLP, and regulatory requirements.
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Clinical Research Associate
3 days ago
Guntur, Visakhapatnam, Warangal, India Clininfotech Full timeManage clinical trials and studies pertaining to biotechnological and pharmaceutical products, drugs and procedures. Conducts research to ensure these products are safe. Ordering, tracking, and managing IP and trial materials. Required Candidate profileKnowledge of the pharmaceutical industry, terminology, and practices. Knowledge of FDA regulations and...
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Clinical Data Management
2 days ago
Bengaluru, Chennai, Hyderabad, Nagpur, Pune, Visakhapatnam, India Clininfotech Full timeCoordinate and manage clinical trials from initiation to completion, ensuring compliance with regulatory guidelines and study protocols.Should have knowledge in Clinical Data Management EDC Edit Checks SAE Reconcillation Required Candidate profileMaintain study supplies, track data collection, and support data analysis, ensuring high-quality and ethical...
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Werum System Administrator
7 days ago
visakhapatnam, India beBeePASXEngineer Full timeJob Title: Werum PAS-X EngineerKey Responsibilities:Install and upgrade WERUM PAS-X on server client architecture.Configure system administration including PAS-X versions 3.1.8, 3.2.1, or 3.30.Service configuration and synchronize users with LDAP/AD.Printing and console functionality.System Administration:Import/export knowledge of SAP-MES Interface.File...
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Clinical Imaging Training Expert
6 days ago
visakhapatnam, India beBeeMedicalImaging Full timeClinical Application SpecialistJob OverviewWe are seeking a highly skilled Clinical Application Specialist to join our team.Key Responsibilities:Develop and execute clinical application training for health systems, hospitals, diagnostic imaging, and oncology centers.Enhance customer satisfaction and productivity by providing exceptional application training...
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visakhapatnam, India beBeeClinical Full timeStatistical Programmer: Clinical Development Expert Sponsor-dedicated statistical programmers are in high demand, and this is an exciting opportunity to join a dynamic team.This position reports to the Director, Biostatistics and Programming in a global pharmaceutical company. The ideal candidate will work independently with minimal supervision, tracking...
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AI Solutions Developer
5 days ago
visakhapatnam, India beBeeArtificialIntelligence Full timeAbout this RoleWe are seeking a skilled AI Engineer to design and deploy advanced artificial intelligence systems for pharmaceutical applications.Main Responsibilities:Develop and implement agent-based AI systems for healthcare and pharma use cases.Fine-tune foundation models for oncology and clinical trial data analysis.Collaborate with cross-functional...
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Senior Software Developer
5 days ago
visakhapatnam, India beBeeRProgramming Full timeSoftware Development PositionWe are seeking a skilled Senior Programmer to develop and maintain software applications using R programming.Develop, test, and deploy R codebases for generating CDISC ADaM datasets and tables, listings, and figures in accordance with clinical trial data requirements.Ensure compliance with industry standards and regulatory...
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Senior Programmer
1 week ago
visakhapatnam, India beBeeR Full timeR Programming SpecialistWe are seeking a skilled R programmer to assume the position of R Programming Specialist. This experienced professional will be responsible for developing and maintaining an R codebase used for generating CDISC ADaM datasets, tables, listings, and figures in accordance with clinical trial data requirements.Key Responsibilities:Develop...