" \u003cdiv class=\"ja-job-details\"\u003e \u003ch2 class=\"title\"\u003eClinical Data Associate\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 Associate \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\u003cbr\u003e\u003cbr\u003eBroad Purpose:\u003cbr\u003e\u0026bull; Develop study-related documents or plans under the supervision of the Data Team Manager\u003cbr\u003e\u0026bull; Preparation of Data Management Plans and assist with development of Edit Check Document with the support of a mentor.\u003cbr\u003e\u0026bull; Preparation of clean and erroneous dummy data.\u003cbr\u003e\u0026bull; Perform data review and cleaning of data collected during the trial and raise queries in the database while conducting cleaning activities for eCRF studies.\u003cbr\u003e\u0026bull; MedDRA / WHO-DD Coding with the support of a mentor and/or review of coding.\u003cbr\u003e\u0026bull; Liaise with a variety of different team members to ensure good communication across each study.\u003cbr\u003e\u0026bull; Archiving of studies, including EDC specific documentation.\u003cbr\u003e\u0026bull; Participate in study-specific or vendor audits conducted by sponsors or regulatory agencies, and respond to audit observations, as required.\u003cbr\u003e\u0026bull; Provide guidance and mentoring to less experienced CDA team members.\u003cbr\u003e\u003cbr\u003eQualifications, Skills and Experience\u003cbr\u003e\u0026bull; Bachelor\u0026rsquo;s level degree in life sciences, pharmacy, nursing or equivalent field (highly regarded), or appropriate industry experience.\u003cbr\u003e\u0026bull; Previous experience as a CDA in a Contract Research Organisation (CRO) or Pharma company for at least 2 years.\u003cbr\u003e\u0026bull; Working knowledge of ICH GCP and applicable regulatory requirements.\u003cbr\u003e\u0026bull; Effective written and oral communications skills, including the ability to keep clients, senior management and other stakeholders informed of project updates and other pertinent information.\u003cbr\u003e\u0026bull; An understanding of Privacy Legislation as it applies to the Clinical Trial Environment. \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=\"916934\" value=\"Apply Now\" title=\"Apply Now\" /\u003e \u003c/div\u003e \u003c/div\u003e "