Systems Implementation Leader (m/f/d)

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Beschreibung



Systems Implementation Leader (m/f/d)

Reference: -en
Start: asap
Duration: 12 MM++

Main tasks:
  • Primary point of contact and business partner for Study Management Teams (SMTs) for all clinical systems and services that Systems and Process Excellence (SPE) offer
  • SILs are accountable for the setup, implementation and operations of the PDG suite of clinical operations systems, such as IxRS and eCOA
  • Accountable to, and partners with the SMT and relevant 3rd parties to lead, direct, and Efficiently deliver clinical systems and innovative solutions, in support of clinical trials
  • Manage the end-to-end lifecycle of applicable clinical systems needed for a given study, Including requirements gathering and reviewing, testing, deployment, maintenance, and Closeout
  • Understand business context and SMT goals to effectively partner with and continually
  • Assess the needs of the SMT, to proactively translate business needs into system and Process improvements
  • Serve as first line of contact for triaging all SMT support and service requests for each Clinical study
  • Ensure prompt resolution of system issues, and provides timely and accurate
  • Response to customers, as defined in service level agreements


Main qualifications
  • Bachelor’s degree with relevant certifications in project management (e.g., PMP) Preferred
  • Profound experience in Biotech/Pharmaceutical industry, with relevant experience in systems and processes, and clinical operations or equivalent
  • Experience with the processes and principles of program and customer relationship management and business analysis
  • Up-to-date knowledge of clinical operations processes and information systems
  • Understanding of internal/external system landscape
  • Experience managing third party vendors in delivering quality service as expected
  • Ability to see and anticipate the interrelationship of systems and procedures within a project and understand their interdependencies – Systems thinking
  • Broad knowledge of applied GxP experience in pharmaceutical or Biotech industry with clinical drug development experience
  • Previous experience in clinical trial planning and execution
  • Ability to successfully lead teams or change initiatives through implementation with little Or no oversight. Proven as a successful decisive leader in a strategic multifunctional environment, with proven ability to navigate organizational complexities
  • Knowledgeable with Clinical Operations and Information Systems and processes such as IxRS, eCOA, CTMS, eTMF, RBM, EDC, and Clinical Supply Systems


Main advantages:
  • You will work in an international environment
  • Option for extension



About us:
With over 15 years of experience in the pharmaceutical industry, biotechnology and medical engineering, we know the key contacts at companies that are recruiting for challenging jobs with real potential. The current high demand for staff has opened up exciting opportunities for dedicated professionals looking to develop themselves professionally and to further their careers. As recruitment specialists with an international network of contacts, we can offer you decisive advantages – all completely free of charge. Register with us and reap the benefits of job offers that are both interesting and relevant to your skills and experience.

My contact at Hays:

Referencenumber:
Start
ab sofort
Dauer
12 MM++
(Verlängerung möglich)
Von
Hays AG
Eingestellt
29.06.2019
Ansprechpartner:
Kerstin Werner
Projekt-ID:
1790689
Vertragsart
Freiberuflich
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