{"id":3335885,"url":"https://alion.io/job/iqvia-local-study-project-manager-sponsor-dedicated-3","title":"Local Study Project Manager - Sponsor Dedicated","company":{"id":4918,"name":"IQVIA","domain":"iqvia.com","url":"https://alion.io/company/iqvia","size_band":"5000+","is_staffing_agency":false,"employer_type":"direct","is_intermediary":false,"listed_via":null,"ats_vendor":"Workday","truth_index":{"grade":"B","score":78,"open_postings":523,"ghost_share":0.008,"stale_share":0.839,"repost_share":0.019,"time_to_fill_p50_days":23,"computed_at":"2026-11-02T06:13:15Z"}},"role":"Management","role_family":"Management","seniority":"senior","employment_type":"full_time","work_mode":"on_site","remote_scope":null,"remote_scope_basis":null,"remote_working_hours":null,"hiring_geo_confidence":"structured","locations":["Bratislava, Slovakia","Prague, Czech Republic"],"countries":["SK","CZ"],"hiring_countries":[],"hiring_countries_total":0,"salary":{"min":41600,"max":62400,"currency":"EUR","period":"year","gross":null,"usd_annual":69783},"salary_estimate":null,"experience_years_min":7,"visa_sponsorship":false,"relocation_package":false,"has_equity":false,"technologies":[{"name":"GCP","optional":false}],"status":"live","first_seen_at":"2026-10-26T00:00:00Z","employer_posted_date":"2026-10-26","last_verified_at":"2026-11-02T09:54:17Z","board_verified":true,"closed_at":null,"days_open":7,"trust":{"level":"ok","repost_count":null,"flags":[],"days_open":7},"description":"The Local Study Project Manager leads Local Study Teams at country level to deliver committed components of clinical studies according to agreed resources, budget and timelines complying with IQVIA or Sponsor Procedural Documents and International guidelines such as ICF-GCP as well as relevant local regulations.\nResponsible to ensure the sites are identified, site qualifications performed, set up, initiated, monitored, closed and documentation archived, to ensure site activation, initiation and maintenance of regulatory activities for selected studies, to perform oversight of local regulatory and ethics submission packages, to oversee milestones planning and strategy for study submission, to oversee the study budget.\nMain Responsibilities\nLeads Local Study Team consisting of CRAs and Study Start Up Specialists for assigned studies. Ensures, as required, the clinical and operational feasibility assessment of potential studies is performed to the highest quality.\nCoordinates the site selection process with relevant stakeholders.\nPlans and coordinates applicable local drug activities (from local purchase or reimbursement to drug destruction).\nSets up and maintains the study in applicable systems at study country level as well as local websites as required by local laws and regulations.\nOversees, manages and coordinates monitoring activities from site activation through to study closure at country and site level in accordance with the Monitoring Plan.\nProactively identifies risks and facilitates resolution of complex study problems and issues.\nOrganizes regular Local Study Team meetings on an agenda driven basis.\nReports study progress/update to the Global Study Associate Director/Global Study Team.\nAssists in forecasting study timelines, resources, recruitment, budget, study materials and drug supplies.\nEnsures relevant systems required to facilitate business critical, license to operate activities (for example, Regulatory Submissions) are set-up, updated and access is organized at country level.\nEnsures accurate payments related to the study are performed according to local regulations and agreements.\nParticipates in training and coaching new members of the Local Study Team ensuring compliance with ICG-GCP and IQVIA or Sponsor Procedural Documents.\nEnsures completeness of the applicable TMF system and ensures essential documents are uploaded in a timely manner to maintain “Inspection Ready” status of applicable systems.\nPlans and leads activities associated with audits and regulatory inspections in liaison with Quality Assurance.\nOversees the execution of Site Activation and/or Maintenance for assigned studies in accordance with the agreed Start Up strategy, adhering to project timelines.\nEnsures collaboration across Regulatory and Start Up & Site Activation, including communication with regions and countries, to successfully deliver the agreed project scope.\nProvides specialist regulatory and technical scientific support to Start Up team.\nDetermines regulatory strategy/expectations and parameters for submissions and all necessary authorizations.\nAssesses and reviews the regulatory landscape and contributes to the collection, interpretation, analysis and dissemination of accurate regulatory intelligence to support assigned studies.\nEnsures accurate completion and maintenance of internal systems, databases, tracking tools, timelines and project plans with project specific information.\nRequired Skills and Qualifications\nBachelor's Degree Life sciences or related field.\n7 years’ relevant experience in a scientific or clinical environment. Equivalent combination of education, training and experience.\nKnowledge of Oncology therapeutical area.\nProven work experience in Phase III studies.\nStrong negotiation and communication skills with ability to challenge.\nExcellent interpersonal skills and strong team player.\nProven ability to work through others to deliver results to the appropriate quality and timeline metrics on complex projects.\nThorough understanding of regulated clinical trial environment and in-depth knowledge of drug development process, including site monitoring experience.\nDemonstrated proficiency in using systems and technology to achieve work objectives.\nGood regulatory and technical writing skills.\nStrong knowledge and ability to apply Clinical Practice (GCP) and International Conference on Harmonization (ICH) guidelines and applicable regulatory guidelines.\nExcellent understanding of study financial management.\nProven ability to work on multiple projects balancing competing priorities.\nVery good knowledge of Slovak or Czech language and English language.\nWillingness to travel occasionally.\nPlease note: due to sponsor requirements for the role only candidates based in the listed location/s will be considered. Any applications from candidates based outside of these locations will not be considered.\nIQVIA is a leading global provider of clinical research services, commercial insights and healthcare intelligence to the life sciences and healthcare industries. We create intelligent connections to accelerate the development and commercialization of innovative medical treatments to help improve patient outcomes and population health worldwide. Learn more at https://jobs.iqvia.com\nIQVIA is committed to integrity in our hiring process and maintains a zero tolerance policy for candidate fraud. All information and credentials submitted in your application must be truthful and complete. Any false statements, misrepresentations, or material omissions during the recruitment process will result in immediate disqualification of your application, or termination of employment if discovered later, in accordance with applicable law. We appreciate your honesty and professionalism.\nThe potential base pay range for this role, when annualized, is 41 600,00 € - 62 400,00 €. The actual base pay offered may vary based on a number of factors including job-related qualifications such as knowledge, skills, education, and experience; location; and/or schedule (full or part-time). Dependent on the position offered, incentive plans, bonuses, and/or other forms of compensation may be offered, in addition to a range of health and welfare and/or other benefits.","description_format":"text","description_chars":6251,"description_truncated":false,"requirements":{"experience_years_min":7,"management_years_min":null,"team_size_min":null,"manages_managers":false,"education":{"level":"bachelor","optional":false},"security_clearance":false,"languages":[{"language":"Slovak","level":"All levels","optional":false},{"language":"Czech","level":"All levels","optional":false},{"language":"English","level":"All levels","optional":false}]},"benefits":[],"hiring_locations":[],"hiring_excludes":[],"relocation_offered":false,"industries":["Clinical Trial Services (CRO)","Health Data & Interoperability"],"lifecycle":[{"event":"open","at":"2026-10-27T13:45:59Z"}],"visa":[],"liveness":{"score":63,"band":"ok","label":"Likely open","p_open":1,"p_active":0.629,"p_room":1,"age_days":7,"expected_fill_days":23,"reasons":["conf:1","stale_co","velocity","win:early","comp:brand"],"computed_at":"2026-11-02T06:13:15Z"},"pay":{"stated_usd_annual":69783,"is_top_pay":false},"html_url":"https://alion.io/job/iqvia-local-study-project-manager-sponsor-dedicated-3","json_url":"https://alion.io/job/iqvia-local-study-project-manager-sponsor-dedicated-3.json","meta":{"generated_at":"2026-11-02T14:16:27Z","cache_seconds":300,"methodology":"https://alion.io/methodology","terms":"https://alion.io/terms","contact":"https://alion.io/contact","api":"https://alion.io/developers","about":"Alion is a live layer of people, companies and AI agents: who they are, whether they are real and active right now, what they do and how to work with them, readable by people and by agents and paid per call.","catalog":"https://alion.io/catalog.json","usage":{"tier":"crawler_verified","counted_by":"address","units_charged":1,"used_today":19676,"day_limit":null,"remaining_today":null,"minute_limit":300,"resets_at":"2026-11-03T00:00:00Z"}},"offers":[{"id":"company.slices","title":"One company in depth, by slice","status":"live","price":{"credits":0.02,"usd":0.002,"plus_per_slice":{"credits":0.05,"usd":0.005}},"unit":"per company, plus each slice with data","note":"the employer in depth","call":{"mcp_tool":"get_company","arguments":{"id":4918},"rest":"https://alion.io/mcp/rest/get_company?id=4918"},"human":"https://alion.io/catalog?offer=company.slices&for=job%2Fiqvia-local-study-project-manager-sponsor-dedicated-3"},{"id":"market.stats","title":"A market slice: pay, demand and time to fill","status":"live","price":{"credits":1,"usd":0.1},"unit":"per slice","note":"pay, demand and time to fill for this role and place","call":{"mcp_tool":"market_stats"},"human":"https://alion.io/catalog?offer=market.stats&for=job%2Fiqvia-local-study-project-manager-sponsor-dedicated-3"},{"id":"job.search","title":"Open jobs by role, technology, place, pay and visa","status":"live","price":{"credits":0.02,"usd":0.002},"unit":"per posting in a list","note":"similar open postings","call":{"mcp_tool":"search_jobs"},"human":"https://alion.io/catalog?offer=job.search&for=job%2Fiqvia-local-study-project-manager-sponsor-dedicated-3"},{"id":"company.verify","title":"Is this company real and active right now","status":"pilot","price":null,"unit":"per company","request":{"url":"https://alion.io/catalog/request","method":"POST","body":"{\"offer\": \"company.verify\", \"for\": \"job/iqvia-local-study-project-manager-sponsor-dedicated-3\", \"note\": \"what you need it for\"}"},"human":"https://alion.io/catalog?offer=company.verify&for=job%2Fiqvia-local-study-project-manager-sponsor-dedicated-3"}],"agent":{"mcp":"https://alion.io/mcp/jobs","mcp_open":"https://alion.io/mcp/open","next":[{"tool":"get_job","arguments":{"id":3335885}},{"tool":"search_jobs","arguments":{"company":"iqvia.com","detail":"compact"}},{"tool":"match_people","arguments":{"job_id":3335885},"note":"people open to offers who fit this vacancy"}],"note":"The same data through MCP tools: https://alion.io/mcp/open needs no sign-in (compact searches, postings, people); https://alion.io/mcp with an Alion account has everything. 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