Study Start-up Specialist - (1805642) in Spain at IQVIA
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España
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Study Start-up Specialist - (1805642) in Spain at IQVIA Date Posted : 10 / 2 / 2018 Job Snapshot

  • Employee Type : JTNS
  • Location : Spain
  • Job Type : Clinical Research & Monitoring
  • Experience : At least 3 year(s)
  • Date Posted : 10 / 2 / 2018
  • Job ID : 1805642 Job Description Join us on our exciting journey! IQVIA is The Human Data Science Company , focused on using data and science to help healthcare clients find better solutions for their patients.
  • Formed through the merger of IMS Health and Quintiles, IQVIA offers a broad range of solutions that harness advances in healthcare information, technology, analytics and human ingenuity to drive healthcare forward.

    PURPOSE Manage and perform tasks at country level associated with Regulatory, Start-Up (RSU) and Maintenance activities in accordance with applicable local and / or international regulations, standard operating procedures (SOPs), project requirements and contractual / budgetary guidelines.

    May participate in pre-award activities, proposals and oversights of the scope of work at country level. RESPONSIBILITIES

  • Serve as Single Point of Contact (SPOC) in assigned studies for investigative sites, RSU Team Lead, Clinical Operations, Feasibility, Site Identification, Project Leadership and GICS.
  • Ensure adherence to standard operating procedures (SOPs), work instructions (WIs), quality of designated deliverables and to project timelines.

    Where applicable, act as a Country Lead for projects with no regional Lead assigned.

  • Perform Regulatory, Start-up and Maintenance activities according to applicable regulations, SOPs and work instructions.
  • Prepare site regulatory documents, reviewing for completeness and accuracy.
  • Review, prepare and negotiate site contracts and budgets with sites, if applicable.
  • Ensure accurate completion and maintenance of internal systems, databases and tracking tools with project specific information.
  • Ensure contracts are fully executed, regulatory documents and approvals are granted, IP Release authorized and specific project deliverables are completed.
  • Review and provide feedback to management on site performance metrics.
  • Review, establish and agree on project planning and project timelines. Ensure overall project efficiency and adherence to project timelines.
  • Ensure monitoring measures are in place and implement contingency plan as needed.

  • May contribute to the collection, interpretation, analysis and dissemination of accurate regulatory intelligence to support assigned studies and wider company, as required.
  • May assist in pre-award activities including bid defenses, proposals and oversights of the scope of work at country level.
  • May provide input into contract and budget template development.
  • May support importation activities.
  • May have direct contact with sponsors on specific initiatives.
  • May act as Local Regulatory, Ethics and Contract Expert and reviewer of ICF.
  • May act as mentor, and prepare and deliver country-specific training, for less experienced staff.
  • May participate in feasibility and / or site identification activities.
  • May perform Site Selection Visits if a trained monitor.
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