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ICON plc
ICON plc
KonsultavimasLogistikaSveikatos priežiūra
ICON plc yra pasaulinė sutartinių tyrimų organizacija, teikianti paslaugas sveikatos priežiūros ir farmacijos sektoriams. Jos veikla apima klinikines, konsultavimo ir komercines paslaugas, padedančias vykdyti vaistų kūrimą nuo ankstyvųjų tyrimų iki veiklos po pateikimo į rinką. Įmonė teikia decentralizuotų klinikinių tyrimų, širdies saugumo vertinimo, ankstyvosios klinikinės laboratorinės veiklos, medicininio vaizdinimo, reguliacinės žvalgybos ir realaus pasaulio įrodymų sprendimus. ICON plc taip pat turi terapinių sričių kompetencijos, įskaitant širdies ir kraujagyslių ligas, onkologiją, vidaus ligas, ląstelių ir genų terapijas bei biologiškai panašius vaistus. Derindama duomenų analizę su į pacientą orientuotais metodais, įmonė padeda plėtoti klinikines programas.
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Darbai įmonėje

Clinical Data Science Manager – Trivandrum Onsite

Lead clinical data management teams supporting ICON’s sponsor-dedicated research services. Oversee people, delivery, quality, compliance, client relationships, resources, and operational improvement.

INIndijaDarbas vietojeVisas etatasJaunesnysis specialistasVidutinis lygisDiplomas nebūtinasPrivaloma Kalba: anglųKlinikiniai tyrimai
Google Cloud Platform

Aprašymas

  • Lead operations and people management for Clinical Data Coordinators, Clinical Data Management Specialists, and other Data Management professionals
  • Provide line management, coaching, and mentoring across designated projects and functions
  • Conduct performance reviews, career discussions, and succession planning
  • Assess capability gaps and put targeted development plans in place
  • Support recruitment, interviewing, onboarding, workforce planning, and resource coordination
  • Manage Data Management delivery to agreed timelines, quality standards, and budgets
  • Assign resources and workloads to improve productivity and delivery performance
  • Track operational metrics, productivity, quality patterns, and capacity projections
  • Oversee project risks, issues, and escalations
  • Ensure deliverables satisfy regulatory obligations, sponsor requirements, and ICON quality standards
  • Maintain adherence to ICH-GCP, applicable regulations, sponsor expectations, and ICON SOPs
  • Represent Data Management in audits, inspections, and quality assessments
  • Lead quality management activities and ongoing process improvement
  • Encourage the adoption of innovative technology, automation, and data-led solutions
  • Help develop departmental processes, tools, methodologies, and transformation initiatives
  • Manage client and sponsor relationships and provide strategic guidance in meetings and governance reviews
  • Report project progress, risks, mitigation actions, and operational updates to stakeholders
  • Represent ISS Data Management in client visits, business development activities, conferences, forums, audits, and inspections
  • Support onboarding, contingent workforce administration, freelancer oversight, and related operational activities
  • Undertake additional responsibilities and strategic initiatives that advance organizational objectives

Reikalavimai

  • Substantial Clinical Data Management experience spanning the complete clinical trial lifecycle
  • Broad experience using multiple EDC systems, data review platforms, and clinical reporting tools
  • At least two years of people management experience covering performance management, workforce planning, recruitment, coaching, and career development
  • Proven ability to manage project delivery, operational measures, and cross-functional stakeholder relationships
  • Experience supporting client engagements and sponsor communications
  • Prior experience managing Team Leads or comparable supervisory positions
  • Experience leading global or cross-functional teams in a matrix organization
  • Familiarity with process improvement, quality management systems, and operational excellence programs
  • Strong knowledge of GCP, ICH guidelines, regulatory obligations, and clinical data management practices
  • Demonstrated leadership and sound decision-making skills
  • Strong project management, planning, and organizational capabilities
  • Ability to balance multiple priorities in a changing and fast-paced environment
  • Strong analytical and problem-solving ability
  • Excellent verbal, written, presentation, and stakeholder communication skills
  • Ability to influence, collaborate, and build effective relationships across organizational levels
  • Meticulous attention to detail and a consistent focus on quality
  • Ability to perform effectively under pressure while meeting quality and delivery commitments
  • Legal authorization to work in the country where the position is based

Privalumai

  • Competitive base pay with performance-based incentives
  • Health and wellbeing programmes, including medical, dental, and vision coverage where available
  • Retirement and pension programmes
  • Life assurance and disability protection
  • Employee assistance services and wellbeing resources
  • Training and career development through structured learning programmes and progression pathways

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ARArgentinaBOBolivijaBRBrazilijaCLČilėCOKolumbijaCRKosta RikaCUKubaDODominikos RespublikaECEkvadorasGTGvatemalaHNHondūrasHTHaitisMXMeksikaNINikaragvaPAPanamaPEPeruPRPuerto RikasPYParagvajusSVSalvadorasUYUrugvajusVEVenesuelaNuotolinisVisas etatasJaunesnysis specialistasDiplomas nebūtinasPrivaloma Kalba: anglųPrivaloma Kalba: ispanųVertėjas

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