Clinical EDC Systems Specialist
5 hours ago
Job Title: Clinical EDC System SpecialistThis role involves creating eCRF specifications, designing, developing and validating clinical trial setup processes.Create edit check specifications and setup edit checks at trial level.Implement UAT scripts to test the setup of the clinical study.Setup different instances of study URL such as UAT, production, testing etc.Manage blinded and unblinded study configurations.Key Responsibilities:As a senior EDC specialist, you will be responsible for:Being the subject matter expert (SME) for all EDC database related activities.Setting up, configuring, validating and integrating other modules within the EDC ecosystem such as coding, integration of IRT, safety system, local labs etc.Understanding when custom functions are required within EDC systems.Troubleshooting database setup as per study needs.Preparing, testing and implementing post-production changes as per study needs.Partnering with team members to establish technology standards and governance models.Overseeing system delivery lifecycle in collaboration with partners including Clinical Operations, Clinical Supplies, IT, and Quality organizations.Ensuring adoption of new capabilities and business processes.Coordinating with clinical technology vendors to ensure established milestones are met with the highest degree of quality.Working with leaders to resolve issues affecting the delivery of clinical trials.Collaborating with data engineers and data management programmers on study-level integrations and deliveries.Leading technology vendor oversight activities.Partnering with team members, technology vendors, and CRO partners to avoid and resolve risks.Confirming archival and inspection readiness of all Clinical Technology Trial Master File (TMF) documents.Participating in preparing function for submission readiness and may represent Clinical Information Operations (CIO) group in a formal inspection or audit.Tracking study deliverables and evaluating study metrics to mitigate risk for major data management deliverables.Adapting to new ways of working using technology to accelerate clinical trial setup.
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Medical Imaging Systems Specialist
2 hours ago
varanasi, India beBeeClinical Full timeClinical Application Specialists play a pivotal role in driving the adoption of advanced medical imaging systems within healthcare institutions.Key objectives include ensuring customer satisfaction with product performance and application training. Their work directly impacts revenue growth through excellent services provided to customers.Developing...
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Clinical Data Specialist
4 days ago
varanasi, India beBeeMedicalCoder Full timeJob Title: Clinical Data SpecialistAbout the Role:We are seeking a highly skilled medical coder to work with our inpatient services team, ensuring accurate and efficient coding of patient data.Key Responsibilities:Coding patients’ diagnoses and procedures using ICD-10-CM/PCS and MS-DRG systems.Maintaining up-to-date knowledge of Official Coding...
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varanasi, India beBeeSpecialist Full timeSenior Medical Specialists Sought for Nationwide Clinical EngagementThis is an exceptional opportunity to expand your clinical expertise and contribute to the delivery of high-quality, patient-centered care.As a Senior Medical Specialist with our organization, you will have the chance to work flexibly from your own clinic, hospital, or home, without...
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Clinical Specialist
1 week ago
varanasi, India beBeeCardiologist Full timeMedical PractitionerIdentify and report ECGs accurately and promptly within the turnaround time and provide guidance to healthcare professionals.Review patient ECGs and dispatch reports to hospitals, clinics, diagnostic centres and nursing homes around the clock without delay to save critical patients.Ensure support for healthcare professionals over the...
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Neuroradiologist - Clinical Expert
1 week ago
varanasi, India beBeeClinical Full timeJob Title: Clinical Expert in Advanced Robotic Surgery and Medical AIWe are seeking a motivated and skilled professional to collaborate with us as Subject Matter Experts (SMEs) on advanced robotic surgery and medical AI projects. This role offers complete flexibility, allowing you to work part-time and fully remote (flexible hours).Manual data annotation...
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Clinical Trials Assurance Specialist
1 week ago
varanasi, India beBeeQuality Full timeAssuring Clinical Trial Quality:About the RoleAudit clinical research sites across phases I–IV, ensuring compliance and quality standards are met.Responsibilities:Review CRFs, informed consent forms, and regulatory documents to identify areas for improvement.Conduct thorough site audits and provide actionable feedback to support corrective actions.Support...
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Senior Clinical Programmer Specialist
1 week ago
varanasi, India beBeeData Full timeJob Title Statistical Data Analyst Develop and maintain datasets, TLFs, and analytical outputs for clinical trials.Support Oncology studies by ensuring accuracy and regulatory compliance in programming deliverables.Contribute to ISS/ISE activities, including dataset integration and analysis.The role requires proficiency in R programming and SAS programming,...
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Chief Data Stewardship Specialist
5 days ago
varanasi, India beBeeDataGovernance Full timeData Governance Architect role entails conceptualizing and implementing data governance solutions utilizing platforms such as Alation, Collibra, and Informatica EDC/AXON.
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Metabolic Disorder Specialist
3 days ago
varanasi, India beBeeEndocrinologist Full timeJob Title: Metabolic Disorder SpecialistThe role of a Metabolic Disorder Specialist involves providing high-quality care within their division, diagnosing and treating complex conditions, managing patient care plans, collaborating with a multidisciplinary team, and contributing to the supervision and training of junior medical staff.Patient Care is a vital...
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Clinical Site Auditor
6 days ago
varanasi, India beBeeQuality Full timeJob Opportunity:Clinical site auditors are responsible for ensuring compliance and quality at clinical trial sites. This includes conducting site audits, reviewing documentation, and verifying adherence to protocols, GCP, GLP, and regulatory requirements.Audits will be conducted of clinical research sites across phases I-IV.CRFs, informed consent forms, and...