" \u003cdiv class=\"ja-job-details\"\u003e \u003ch2 class=\"title\"\u003eClinical Data Manager\u003c/h2\u003e \u003cdiv class=\"meta\"\u003e \u003cul class=\"classifications\"\u003e \u003cli data-id=\"23519\"\u003e Biometrics \u003c/li\u003e \u003cli data-id=\"23520\"\u003e Clinical Data Manager \u003c/li\u003e \u003cli data-id=\"23521\"\u003e India \u003c/li\u003e \u003cli data-id=\"23522\"\u003e Permanent / Full Time \u003c/li\u003e \u003c/ul\u003e \u003cp class=\"date-posted\"\u003e 16/10/2026 \u003c/p\u003e \u003c/div\u003e \u003cdiv class=\"description\"\u003e \u003cstrong\u003eWho are we?\u003c/strong\u003e\u003cbr\u003e We\u0026rsquo;re Avance Clinical a Contract Research Organisation. We offer specialised services supporting drug development for the pharmaceutical and biotechnology industry. We have a rich history in this area with our founding roots dating back to the 1980\u0026rsquo;s. If you already work in this industry you\u0026rsquo;ll know that we are experts in our field.\u003cbr\u003e \u003cstrong\u003eWhy should you join Avance Clinical?\u003c/strong\u003e\u003cbr\u003e We appreciate that our most important asset is our people. We offer a fun, friendly\u0026nbsp;work environment and a culture that values honesty and respect. We have a strong sense of team. We genuinely appreciate each individual but recognise the collective when achieving success.\u003cbr\u003e We are committed to creating a flexible work environment for our people by supporting them to balance their work commitments and personal needs, both now and into the future.\u003cbr\u003e \u003cstrong\u003eResponsibilities\u003c/strong\u003e\u003cbr\u003e \u003cul\u003e \u003cli\u003ePreparation of Data Management Plans.\u003c/li\u003e \u003cli\u003ePreparation or review of Edit Check Document.\u003c/li\u003e \u003cli\u003eDevelopment and review of Case Report Forms (CRFs) and completion guidelines in line with the database and protocol.\u003c/li\u003e \u003cli\u003ePreparation of clean and erroneous dummy data.\u003c/li\u003e \u003cli\u003eDatabase Validation (testing data entry screens and edit checks using dummy data).\u003c/li\u003e \u003cli\u003eProvide training to site, Sponsor and other staff in the use of eCRF systems.\u003c/li\u003e \u003cli\u003eResolution of Quality Assurance (QA) comments.\u003c/li\u003e \u003cli\u003ePerform data review and cleaning of data collected during the trial.\u003c/li\u003e \u003cli\u003ePerform Quality Control on study data prior to lock.\u003c/li\u003e \u003cli\u003eAct as Data Project Manager including interaction with Clinical Project Manager, interact with site/ client/ external vendors, perform overall Project Management and timeline management.\u003c/li\u003e \u003c/ul\u003e \u0026nbsp;\u003cbr\u003e \u003cstrong\u003eWhat you\u0027ll need to succeed\u003c/strong\u003e\u003cbr\u003e \u003cul\u003e \u003cli\u003eOrdinary degree in the appropriate discipline or equivalent experience.\u003c/li\u003e \u003cli\u003e4-5 years experience in the pharmaceutical industry / CRO working in a GCP environment.\u003c/li\u003e \u003cli\u003eKnowledge of ICH GCP Guidelines, medical terminology and clinical trials process.\u003c/li\u003e \u003cli\u003eExperience in EDC/e-CRF systems\u003cem\u003e.\u003c/em\u003e\u003c/li\u003e \u003cli\u003eIntermediate MS Office Suite.\u003c/li\u003e \u003c/ul\u003e \u003c/div\u003e \u003cdiv class=\"apply\"\u003e \u003ca class=\"back-link\" href=\"#\" title=\"Back to search results\"\u003eBack to search results\u003c/a\u003e \u003cinput type=\"button\" class=\"ja-button\" data-job-id=\"916935\" value=\"Apply Now\" title=\"Apply Now\" /\u003e \u003c/div\u003e \u003c/div\u003e "