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Responsibilities / Duties- · Conduct project specific configurations in Safety systems · Maintain and document system configuration based on initial requirements and any subsequent changes Evaluate proposed project ideas / software changes through technical impact analysis and estimated business value to contribute to decision-making. Develop and document standard and ad hoc reports from the safet
Responsibilities / Duties- ? Conduct project specific configurations in Safety systems ? Maintain and document system configuration based on initial requirements and any subsequent changes Evaluate proposed project ideas / software changes through technical impact analysis and estimated business value to contribute to decision-making. Develop and document standard and ad hoc reports from the safet
SAS Base & Macros #statistical #inferentialstatistics #statisticians #statistics #stat #probability #statisticsandprobability #statslove #statlove #mathematics #inferential #statistic #statsforlife #biostatisticians #statsforlifee #estimation #significance #inference #nonparametric #parametric #datascience #bigdata #analytics #interpretation #testing Job Description About Accenture: Accenture
SAS Clinical #statistical #inferentialstatistics #statisticians #statistics #stat #probability #statisticsandprobability #statslove #statlove #mathematics #inferential #statistic #statsforlife #biostatisticians #statsforlifee #estimation #significance #inference #nonparametric #parametric #datascience #bigdata #analytics #interpretation #testing Job Description : Minimum 5 years of experience
SAS Programmer (Bangalore,Mumbai,Pune,Home-Based) #statistical #inferentialstatistics #statisticians #statistics #stat #probability #statisticsandprobability #statslove #statlove #mathematics #inferential #statistic #statsforlife #biostatisticians #statsforlifee #estimation #significance #inference #nonparametric #parametric #datascience #bigdata #analytics #interpretation #testing Develop and
Senior Clin process Assoc #lifesciencegraduate #nagpurjobs #apportunities #clinicalresearchinstitute #smo #clinicalresearchcareers #clinicalresearchtrials #medicalresearch #healthcare #biology #pharmacovigilance #clinicalresearchtraining #education #bpharma #research #clinicalresearchers #nurse #clinicalresearchjobs #crc #pharmaceuticals #pharma #clinicaltrialsguru #clinicaldatamanagement #cral
Senior Clinical Data Specialist new #lifesciencegraduate #nagpurjobs #apportunities #clinicalresearchinstitute #smo #clinicalresearchcareers #clinicalresearchtrials #medicalresearch #healthcare #biology #pharmacovigilance #clinicalresearchtraining #education #bpharma #research #clinicalresearchers #nurse #clinicalresearchjobs #crc #pharmaceuticals #pharma #clinicaltrialsguru #clinicaldatamanage
Senior CRA 1 #lifesciencegraduate #nagpurjobs #apportunities #clinicalresearchinstitute #smo #clinicalresearchcareers #clinicalresearchtrials #medicalresearch #healthcare #biology #pharmacovigilance #clinicalresearchtraining #education #bpharma #research #clinicalresearchers #nurse #clinicalresearchjobs #crc #pharmaceuticals #pharma #clinicaltrialsguru #clinicaldatamanagement #cralife #sciences
Site Specialist #freshersjobs #helpinghand #Engineeringjobs #jobs #itjobs #hrjobs #fresher #opportunities #intern #recruitment #engineeringjobs #recruiting #vacancy #engineer #recruitment #jobs # #fresher #hiring #employment #experience #data #jobseekers #collegestudents #internship Qualified candidate has an Associate's degree with equivalent work experience or equivalent years' relevant wo
Software Developer #pythonprogramming #developerlife #php #coderlife #computer #machinelearning #linux #codingisfun #daysofcode #coders #android #programmerslife #engineer #devlife #fullstackdeveloper #softwaretesting #frontenddeveloper #dev #webdev #datascience #computerengineering #softwaredevelopers #javascriptdeveloper #artificialintelligence #informationtechnology #reactjs #peoplewhocode #
Design, setup and maintain automated testing processes for Xcellerate product development and support. Create an automation test bed, configure testing tools for all products based on current test scripts and processes and generate automated reports conforming to Labcorp's quality standards using industry best practices.Oversee all aspects of quality assurance including establishing metrics, applyi
Ensuring that the IST investigator is providing study updates in tool as applicable to the customer viz. regulatory updates, enrolment data, confirming that safety information is being transferred to customer as required, notification of any amendments to either the protocol or informed consent. Reviewing that the agreed upon contractual milestones are being met and raising to customer for any thre
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Ensure electronic vendor data contains all protocol specified parameters, is in correct format and data populates to the specified fields and patients correctly May support LDM in the development of the Data Transfer Agreement and Data Transfer Specifications for vendor data transfers. Review data discrepancies generated by study specific edit checks for External data and perform the subsequent que
Perform aggregate review of clinical data by patient, site and / or project to identify data trends patient safety, compliance, etc. and / or data inconsistencies that require further investigation. Generate, resolve, and track queries to address problematic data identified during data review activities. Apply quality control procedures and checks to ensure data quality standards client and Covance
Perform aggregate review of clinical data by patient, site and / or project to identify data trends (patient safety, compliance, etc.) and / or data inconsistencies that require further investigation. Generate, resolve, and track queries to address problematic data identified during data review activities. Apply quality control procedures and checks to ensure data quality standards (client and Cova
Review clinical trial data in accordance with Data Management Plans and applicable standardized data management processes SOPs, Work Instructions, etc. to identify erroneous, missing, incomplete, or implausible data. Run ancillary programs e.g., diagnostics, special listings, reconciliation discrepancy listings used to suppott the review of clinical trial data. Generate, resolve and track querie