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QUALITIS SA – CLINICAL STUDY LEADER – ATHENS

Qualitis SA, part of Optimapharm Group, requires for immediate employment a Clinical Study Leader (Position Code: Q/CSL/CL), who will be fully involved in the clinical trials of an International Pharmaceutical Company in Athens.

Our Company provides an excellent benefits package, including:

  • Competitive Salary
  • Company Car/Mobile Phone/Private Health Insurance
  • Annual Bonus

Job responsibilities mainly include:

  • Develops and manages comprehensive clinical trial timelines and metrics and ensures that they are met.
  • Oversees that clinical trial progress is reported and tracked and assures that proper documentation is maintained and archived.
  • Prepares and implements trial-specific training programs and materials for clinical research staff (CRAs/CTAs).
  • Assists the planning of regulatory/ethics committee approval process.
  • Provides guidance and mentoring to clinical research staff and investigational sites.
  • Reviews the site visit reports.
  • Develops, tracks and updates clinical trial budgets.
  • Ensures audit-ready condition of clinical trial documentation. Participates in the planning of quality assurance activities and coordinates resolution of audit findings
  • Attends meetings to discuss handling/improving people planning process.

The ideal candidates should fulfill the following qualifications/requirements:

  • Hold a University and Postgraduate Degree in Health Sciences.
  • A minimum of four (4) years of experience as a Senior CRA or one (1) year of experience in a Managerial role within the field of Clinical Research in the Pharmaceutical Industry/CRO Sector.
  • Excellent knowledge of ICH GCP requirements.
  • Exceptional writing and presentation skills.
  • Excellent computer literacy with the MS Office Suite.
  • Ability to multitask and work in a fast-paced environment.
  • Ability to travel on a regular basis.

Candidates should send their CVs in English indicating the position code, at info@qualitis.gr

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