{"id":3237963,"url":"https://alion.io/job/icon-cdc-ii","title":"CDC II","company":{"id":5677,"name":"ICON","domain":"iconplc.com","url":"https://alion.io/company/icon","size_band":"5000+","is_staffing_agency":false,"employer_type":"direct","is_intermediary":false,"listed_via":null,"ats_vendor":"Workday","truth_index":{"grade":"B","score":80,"open_postings":5,"ghost_share":0,"stale_share":1,"repost_share":0,"time_to_fill_p50_days":5,"computed_at":"2026-10-26T05:57:25Z"}},"role":"Sales","role_family":"Sales","seniority":"middle","employment_type":"full_time","work_mode":"on_site","remote_scope":null,"remote_scope_basis":null,"remote_working_hours":null,"hiring_geo_confidence":"structured","locations":["Chennai, India","Thiruvananthapuram, India"],"countries":["IN"],"hiring_countries":[],"hiring_countries_total":0,"salary":null,"salary_estimate":null,"experience_years_min":null,"visa_sponsorship":false,"relocation_package":false,"has_equity":false,"technologies":[{"name":"Good Clinical Practice","optional":false},{"name":"Medidata Rave","optional":false}],"status":"live","first_seen_at":"2026-10-23T00:00:00Z","employer_posted_date":"2026-10-23","last_verified_at":"2026-10-26T21:49:06Z","board_verified":true,"closed_at":null,"days_open":3,"trust":{"level":"ok","repost_count":null,"flags":[],"days_open":3},"description":"CDC IIAt ICON Strategic Solutions, you will work in a sponsor-dedicated model, supported by ICON’s global expertise.\nAs the world’s largest FSP organisation, with over 90 sponsor partnerships, we offer stability, career development and a collaborative environment where your work contributes to the development of treatments that benefit patients worldwide.\nAs a CDC II at ICON, you will design and analyse clinical trials, interpreting complex medical data, and contribute to the advancement of innovative treatments and therapies.\nWhat You Will Do:\nYour role will involve delivering clinical data management work to a high standard, working closely with your team and stakeholders.\nKey responsibilities include:\nAssist Data Management Study Lead in maintenance of eCRF, Data Validation Specifications, and Study Specific Procedures.\nManage clinical and third-party data reconciliation based on edit specifications and data review plans.\nTracks and communicates status of study and task metrics to clinical data scientist, project team, and functional management.\nAddress data related questions and recommend potential solutions.\nIdentify root cause to systematically resolve data issues.\nYour Profile:\nYou will bring relevant clinical data management experience, along with the following qualifications and skills.\nRequired qualifications and experience:\nBachelor's degree in a relevant field, such as Life Sciences or Healthcare.\nIntermediate knowledge of clinical data management within the pharmaceutical or biotechnology industry.\nFamiliarity with data management software and systems (e.g., Medidata, Oracle RDC, or similar).\nStrong attention to detail and the ability to work effectively in a fast-paced environment.\nExcellent communication skills and the ability to collaborate with cross-functional teams.\nKnowledge of regulatory guidelines and standards (e.g., ICH-GCP) is a plus.\nEmployment with ICON is contingent upon having the legal right to work in the country where the role is based.\nRewards & Benefits\nICON offers a competitive and comprehensive total rewards package designed to support your health, wellbeing, and career development.\nBenefits may include:\nCompetitive base salary and performance related incentives\nHealth and wellbeing programmes including medical, dental, and vision coverage where applicable\nRetirement and pension plans\nLife assurance and disability coverage\nEmployee assistance programmes and wellbeing resources\nLearning and development opportunities through structured training and career pathways\nBenefits may vary depending on role and location.\nVisit our careers site to read more about the benefits ICON offers.\nInclusion and Accessibility\nICON is an equal opportunity employer. We are committed to building an inclusive and accessible workplace where everyone feels valued and supported.\nIf you require reasonable accommodations during the recruitment process, please let us know or submit a request here.\nAre you a current ICON Employee? 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