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3 - 7 years
15 - 20 Lacs
Nagpur, Pune
Work from Office
Hi, We are hiring for Leading ITES Company for Lead Data Manager Profile. Job Description Perform day to day Clinical Data Management activities. Work and coordinate with the team to perform data management activities and deliver an error free quality database in accordance with the data management plan and regulator standards. Read and understand the study protocol and the timelines. Perform test data entry in TEST environment, data listing review, data reconciliation and query management tasks. Escalate/Action discrepancy in the clinical data as appropriate. Perform external checks to handle manual discrepancies and action the same. Ensure an error free, quality data with no open queries. ...
Posted 4 months ago
2 - 7 years
9 - 12 Lacs
Pune, Bengaluru, Mumbai (All Areas)
Work from Office
Hi We are hiring for Leading ITES Company for Clinical Data Manager Profile. Role & Responsibilities: Candidate should have 2-5 years of experience of CDM with experience in Conduct Scope of work Perform day-to-day Clinical Data Management activities. Work and coordinate with the team to perform data management activities and deliver an error-free quality database in accordance with the data management plan and regulator standards. Read and understand the study protocol and the timelines. Perform test data entry in the TEST environment, data listing review, data reconciliation, and query management tasks. Escalate/Action discrepancy in the clinical data as appropriate. Perform external check...
Posted 4 months ago
2 - 7 years
15 - 20 Lacs
Nagpur, Bengaluru
Work from Office
Hi We are hiring for the ITES Company for the SAS : J Review Programmer Role Role & responsibilities Programming, specifically Programming, specifically J Review, SQL, R and GitHub. Good to have SAS. Create data cleaning reporting solutions study status metric, and monitoring reports and visualizations required per standard and study specific data review plans. Develop library of reusable checks working closely with data engineers and config specialists. Collaborate with cross functional teams in creating business rules and automated check library across TAU. Serves as a technical resource for creating data analytics to help with data validation and cleaning. Provide programming expertise fo...
Posted 4 months ago
9.0 - 13.0 years
15 - 30 Lacs
hyderabad, chennai, bengaluru
Work from Office
Role : Lead Clinical Database Programmer CDM Exp : 9 to 13 yrs Work Mode : Hybrid / Remote Looking for Immediate Joiners only Area : Study set-up and Migration activities using Rave/Veeva/Oracle Clinical/Inform Function : Clinical data management & Development Sub Function : Development- (eCRF/Edit Checks/custom functions/Clinical Trails/Reports) Responsibilities : Responsible for creation of clinical databases in Rave to support data collection in clinical trial. Drives post-production changes in Rave studies to ensure compliance with protocol amendments. Communicates with data management team and study management teams throughout all the study start-up/ post-production activities to ensure...
Posted Date not available
10.0 - 20.0 years
25 - 40 Lacs
noida
Remote
Position: Data Quality System Testing Consultant Experience: 10+ Years Mode: Remote Time: US EST Hours Objective / Purpose: Create and execute detailed test plans and UAT scripts in Excel and /or ALM testing system based on business requirements and technical specifications to verify study/library functionality in Veeva CDMS and/or Rave EDC system and adherence to standards. Drive study database user acceptance testing activities and ensure the quality of the study build in the EDC system. Ensure accurate delivery of study build with quality deliverables per specification. Participate in the development, maintenance and training rendered on activities around study build and best practices us...
Posted Date not available
3.0 - 5.0 years
4 - 7 Lacs
vadodara, manjusar
Work from Office
Department - Clinical Roles and Responsibilities: End to End clinical data management and pertinent documentation for clinical studies and real-world data collection. Managing vendors for CDM Conducting User Acceptance Testing Provide guidance on training requirements in relation data management System and technical Skills Regulations and Standards 21CFR part 11, GDPR, ISO 27001, SDLC and ISO 62304, CDISC standards Databases & ORM: EDC databases - Clinion, OCRDC, Oracle one, Inform, Open clinica, etc. MS Access Tools: MS office, Power Automate, Power BI, MedDRA, WHODD, Rave, Clinion, Research Manager Understanding of the Medical Device industry
Posted Date not available
5.0 - 10.0 years
9 - 14 Lacs
pune, bengaluru
Work from Office
Our Clinical/Drug Development division displays a substantial history of contributing to numerous client projects with significant results in drug development. The Drug Development RD Technologists possess a deep understanding of technological solutions for clinical development processes including clinical study design, data management, analytics, and quality risk management platforms and products. They are well-versed in software related to clinical trial protocol design, electronic data capture (EDC), external data capture, data conformance, transformation, analysis, and reporting. Our team is well versed about industry standards such as CDISC, FHIR, OMOP, and their respective usage. Our t...
Posted Date not available
5.0 - 8.0 years
0 - 0 Lacs
hyderabad
Work from Office
Looking for Trainer Who Provides Offline training on Clinical Data Management On Part time basis Provides training and monitors performance to ensure the team are operating at the highest level to design and deploy clinical databases. Required Candidate profile Should have Experience on clinical data management Entire Work Process EDC SAE Reconciliation. should have Experience on Softwares (Oracle Inform/ Mediidata Rave) Interested Contact - 9133469786
Posted Date not available
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