Ass Manager, Clinical Analytic (BB-BA739)

Encontrado en: Neuvoo CR


Job Overview:

Get ready to redefine what’s possible and discover your extraordinary potential at Covance. Here, you’ll have the opportunity to personally advance healthcare and make a difference in peoples’ lives with your bold ideas and unique point of view. With the support of exceptional people from across the globe and an energized purpose, you’ll be empowered to own your career journey with mentoring, training and personalized development planning. Join us as we speed the delivery of groundbreaking therapies and anticipate tomorrow’s drug development challenges, creating new possibilities for our clients—and your career.

COVANCE  is a leading global drug development services company and we provide support to the Pharmaceutical and Biotechnology industries. We have an exciting opportunity available to join our team.

We are currently recruiting an Associate Manager, EDS in Costa Rica


  • Associates or bachelor’s degree in Medical/Life Science/Computer Science or equivalent combination of education and experience to successfully perform the key responsibilities of the job.
  • Thorough knowledge of ICH Guidelines and GCP including international regulatory requirements for the conduct of clinical development programs, especially as related to data handling and processing.
  • Broad knowledge of drug development process.
  • Knowledge of effective external data management practices.
  • Understanding of global clinical development budgets and relationship to productivity targets.
  • Experience:

  • 5+ years prior experience in the pharmaceutical, biotechnology, medical device/diagnostics, or clinical trial industries to include data management or an equivalent combination of education and experience to successfully perform the key responsibilities of the job.
  • Demonstrated leadership and interpersonal skills. Previous line management experience required or an equivalent of management training.
  • Strong organizational, planning, and critical-thinking skills.
  • Well-polished, inclusive, and engaging communication skills (written and verbal) to support effective interactions with sponsors and internal colleagues.
  • Strong negotiation skills to facilitate, guide, influence, and produce a unified approach within a global, cross-functional environment.
  • Ability to maintain confidentiality of data and information during interaction with staff at all levels.
  • Demonstrated ability to lead teams by example on project strategies, achievement of department goals, objectives, initiative and to encourage team members to seek solutions.
  • In-depth knowledge of clinical trial processes, data management, clinical operations, biometrics, quality management and systems applications to support operations.
  • calendar_todayhace 2 días

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