{"id":208987,"url":"https://alion.io/job/veeva-systems-senior-consultant-clinical-data-programming-2","title":"Senior Consultant - Clinical Data Programming","company":{"id":3288,"name":"Veeva Systems","domain":"veeva.com","url":"https://alion.io/company/veeva-systems","size_band":"1001-5000","is_staffing_agency":false,"employer_type":"direct","is_intermediary":false,"listed_via":null,"ats_vendor":"Lever","truth_index":{"grade":"B","score":80,"open_postings":793,"ghost_share":0.243,"stale_share":0,"repost_share":0.003,"time_to_fill_p50_days":167,"computed_at":"2026-11-01T06:10:25Z"}},"role":"Science & Research","role_family":"Science & Research","seniority":"senior","employment_type":"full_time","work_mode":"remote","remote_scope":"stated_regions","remote_scope_basis":"posting_text","remote_working_hours":null,"hiring_geo_confidence":"structured","locations":["Barcelona, Spain"],"countries":["ES"],"hiring_countries":["ES","DE","FR","AT","BE","BG","HR","CY","CZ","DK","FI","HU","IE","IT","NL","PL","RO","SE","EE","GR","LV","LT","LU","MT","PT","SK","SI"],"hiring_countries_total":27,"salary":{"min":72000,"max":110000,"currency":"EUR","period":"year","gross":null,"usd_annual":123476},"salary_estimate":null,"experience_years_min":5,"visa_sponsorship":false,"relocation_package":false,"has_equity":false,"technologies":[{"name":"Python","optional":false},{"name":"SAS","optional":false},{"name":"SQL","optional":false},{"name":"Veeva","optional":false},{"name":"CDISC","optional":true},{"name":"Rest API","optional":true}],"status":"live","first_seen_at":"2026-09-01T18:00:44Z","employer_posted_date":"2026-09-01","last_verified_at":"2026-11-01T19:30:20Z","board_verified":true,"closed_at":null,"days_open":61,"trust":{"level":"ok","repost_count":0,"flags":["company_stale"],"days_open":60},"description":"The Role\nVeeva's Vault Clinical Data Management System (CDMS) is changing how life sciences companies manage clinical trial data, bringing EDC, coding, and Veeva Data Quality System (DQS) together in one platform. We're looking for a Senior Consultant with life sciences software programming experience to help customers get the most out of EDC while running their trials. This is a full-time, permanent, customer-facing role open to candidates working remotely from the EU or UK.\nWhat You’ll Do\nAct as a trusted advisor to customers and clinical sites, ensuring trial designs are configured to meet their goals, and providing training and mentorship along the way\nWork with customers to interpret clinical protocol requirements and project specifications, applying industry and Veeva best practices\nLead database development activities per the project plan, coordinating with sponsor, CRO, and other vendor teams\nCoordinate with clinical data providers (central labs, ECG, eCOA, IRT, etc.) to configure data transfers\nConfigure forms, rules, and other study items in Vault CDMS, and build custom SQL-based listings for customer data cleaning needs\nRun on-site or remote user acceptance testing, managing feedback, issue resolution, and study acceptance\nSupport requirements gathering and specification writing for study integrations and go-live activities\nFlag risks and contingency plans to project management to keep the project compliant with regulatory and Veeva procedures\nContribute to process, product, and best-practice initiatives, and support developers and testers throughout the project lifecycle\nShare data management activities, challenges, and end-user feedback with the Vault CDMS product team\nConfigure and support data imports into Veeva DQS\nRequirements\n5+ years of experience with EDC clinical software, covering end-to-end data management (database design, data collection, data analysis, query resolution, datasets, statistical reporting)\nSolid understanding of clinical trial processes, particularly around data collection and review\nProgramming experience in languages such as SAS, R, JSON, Python, or SQL, with the ability to pick up new SQL-based languages\nBackground in the life sciences industry (pharma, biotech, medical device, CRO, or academic/public health), with experience across project assessment, planning, development, training, and implementation\nExperience in a customer-facing role, ideally within software professional services or consulting\nAbility to work independently and collaboratively in a fast-paced, dynamic environment while meeting project timelines\nStrong verbal and written communication, interpersonal, and presentation skills\nWillingness to travel up to 10%, potentially including international travel\nNice to Have\nFamiliarity with data management standards (GCDMP, CDISC, SDTMIG, CDASH, ADaM)\nExperience working with system integrators for IVRS, medical coding, eSource, CTMS, eTMF, or similar clinical technologies\nExperience integrating or programming with REST-based APIs\nExperience translating clinical protocols into software specifications, including technical documentation\nExperience with Veeva applications\nLocated near a major life sciences hub\nDegree in Life Sciences, Computer Science, or a related field\nInterviewing with Veeva\nWe value your time and believe in a transparent hiring process. Here is the process you can expect.\nFollow the application process and submit your resume.\nWithin 3 days, you will receive a link to a personality assessment administered by a third party.\nOnce you complete the assessment, our team will review your full application package and follow up via email with our decision.\nIf moving to the interview stage, the process is as follows:A conversation with the hiring manager\nA practical case exercise\nA final conversation with our group's Senior Leader.\n\nOnce all interviews are complete, the manager will be in touch with a final decision. \nPerks & Benefits\nPrivate health insurance\nFlexible paid time off plus local public holidays\nPension / retirement plan contributions\n1% charitable giving program\nCompensation\nTotal compensation: 72,000 - 110,000EUR\nThe total compensation range listed here has been provided to comply with local regulations and represents a potential total compensation range for this role. Please note that actual total compensation may vary within the range above or below, depending on experience and location. We look at compensation for each individual and base our offer on your unique qualifications, experience, and expected contributions. This position's total compensation may be composed of other types of compensation, such as variable bonus and/or stock bonus.","description_format":"text","description_chars":4702,"description_truncated":false,"requirements":{"experience_years_min":5,"management_years_min":null,"team_size_min":null,"manages_managers":false,"education":null,"security_clearance":false,"languages":[]},"benefits":["Health insurance","Retirement plans"],"hiring_locations":[{"name":"Spain","iso":"ES","kind":"country"},{"name":"Germany","iso":"DE","kind":"region"},{"name":"France","iso":"FR","kind":"region"},{"name":"Austria","iso":"AT","kind":"region"},{"name":"Belgium","iso":"BE","kind":"region"},{"name":"Bulgaria","iso":"BG","kind":"region"},{"name":"Croatia","iso":"HR","kind":"region"},{"name":"Cyprus","iso":"CY","kind":"region"},{"name":"Czech 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