" \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 \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 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 \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\u003cbr\u003e\u003cstrong\u003eThe Role\u003c/strong\u003e\u003cbr\u003eThe Clinical Data Manager I (CDM I) performs activities associated with the Data Cleaning activities of Clinical trials to ensure the trial is conducted in accordance with the protocol; company Standard Operating Procedures (SOPs), ICH GCP guidelines and other applicable regulatory requirements.\u003cbr\u003e \u003cbr\u003e\u003cstrong\u003eCore Responsibilities\u003c/strong\u003e\u003cbr\u003e \u003cul\u003e \u003cli\u003eAutonomously Develop study-related documents or plans.\u003c/li\u003e \u003cli\u003eLead the Data management team as the Lead CDM including development of Data Management Plan, eCRF completion Guidelines, Data Edit Checks Document, etc. Perform all activities (Start Up, Conduct and Closeout activities as per the SOPs Including the MedDRA/WHODD coding and/or review).\u003c/li\u003e \u003cli\u003eDevelop effective relationships for assigned Sponsors to successfully manage sponsor grievances and drive strategic partnerships.\u003c/li\u003e \u003cli\u003eRaise data queries in the EDC where discrepancies are identified and work with CRA/site staff to ensure timely and accurate resolution.\u003c/li\u003e \u003cli\u003eEnsure accurate and timely filing as per SOP requirements.\u003c/li\u003e \u003cli\u003eMaintain effective communication across the study team to proactively manage on-going study expectations and issues.\u003c/li\u003e \u003cli\u003eParticipate in study-specific or vendor audits conducted by sponsors or regulatory agencies, and respond to audit observations, as required.\u003c/li\u003e \u003cli\u003eEnsure Serious Adverse Events are reported (initial and follow-up) as per protocol requirements.\u003c/li\u003e \u003cli\u003eOther duties as directed by Line Management or delegate in line with skills, experience and/or qualifications.\u003c/li\u003e \u003cli\u003eDepartmental Responsibilities\u003c/li\u003e \u003cli\u003eFoster the on-going commitment to maintaining a healthy team culture and promoting good morale, by actively participating in regular Data Management Team meetings.\u003c/li\u003e \u003cli\u003eMaintain effective communication with other members of the department.\u003c/li\u003e \u003cli\u003eProactively identify risks related to departmental service provision and assist in their mitigation and resolution.\u003c/li\u003e \u003cli\u003eParticipate in internal Quality Assurance activities as required, including responding to internal audit findings\u003c/li\u003e \u003c/ul\u003e \u003cstrong\u003eOrganisational Responsibilities\u003c/strong\u003e\u003cbr\u003e \u003cul\u003e \u003cli\u003eEmbrace the core values of Avance Clinical and endeavor to display those attributes at all times with clients and staff alike.\u003c/li\u003e \u003cli\u003eCommit to Avance Clinical training programs.\u003c/li\u003e \u003cli\u003eAdhere to Avance quality systems.\u003c/li\u003e \u003cli\u003eAll staff are required to take reasonable care for their own health and safety and that of other personnel who may be affected by their conduct.\u003c/li\u003e \u003cli\u003eThe accountabilities as specified above may be altered in accordance with the changing requirements of the position.\u003c/li\u003e \u003c/ul\u003e \u003cstrong\u003eQualifications, Skills and Experience\u003c/strong\u003e\u003cbr\u003e \u003cul\u003e \u003cli\u003eBachelor\u0026rsquo;s level degree in life sciences, pharmacy, nursing or equivalent field or appropriate industry experience.\u003c/li\u003e \u003cli\u003ePrevious experience as a CDM in a Contract Research Organization (CRO) or Pharma company for at least 2 years.\u003c/li\u003e \u003cli\u003eFormal ICH GCP training and a working knowledge of ICH GCP Guidelines and other applicable regulatory requirements.\u003c/li\u003e \u003cli\u003eClear understanding of the requirement to adhere strictly to client confidentiality.\u003c/li\u003e \u003cli\u003eEffective written and oral communications skills, including the ability to keep clients, senior management and other stakeholders informed of project updates and other pertinent information.\u003c/li\u003e \u003cli\u003eDemonstrated ability to take initiative in problem solving and in exercising good judgment.\u003c/li\u003e \u003cli\u003eAbility to work under pressure in a multi-disciplinary team environment.\u003c/li\u003e \u003cli\u003eWillingness to work in, and be supportive of, a positive and dynamic team culture.\u003c/li\u003e \u003c/ul\u003e \u003cstrong\u003eWhat we offer\u003c/strong\u003e\u003cbr\u003e \u003cul\u003e \u003cli\u003eStimulating work\u003c/li\u003e \u003cli\u003eProject diversity\u003c/li\u003e \u003cli\u003eAn intellectual challenge\u003c/li\u003e \u003cli\u003eAn agile \u0026amp; flexible workplace\u003c/li\u003e \u003cli\u003eOpportunity to progress\u003c/li\u003e \u003cli\u003eStability\u003c/li\u003e \u003cli\u003eSense of community\u003c/li\u003e \u003cli\u003eA leadership team that are working together on a common goal\u003c/li\u003e \u003cli\u003eFlexible work options\u003c/li\u003e \u003cli\u003eGreat tools / tech to do your job\u003c/li\u003e \u003c/ul\u003e \u003cstrong\u003eWhat next?\u003c/strong\u003e\u003cbr\u003e As a growing business we\u0026rsquo;re looking for likeminded people to join us \u0026ndash; we hope that\u0026rsquo;s you.\u003cbr\u003e \u003cul\u003e \u003cli\u003eTo join our team please submit your CV \u0026amp; cover letter as one Microsoft Word document.\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=\"916427\" value=\"Apply Now\" title=\"Apply Now\" /\u003e \u003c/div\u003e \u003c/div\u003e "