Clinical Research Associate
AbbVie, Inc
Buenos Aires , Ciudad Autónoma de Buenos Aires, Argentina
hace 8 días

is a global, research-driven biopharmaceutical company committed to developing innovative advanced therapies for some of the world’s most complex and critical conditions.

The company’s mission is to use its expertise, dedicated people and unique approach to innovation to markedly improve treatments across four primary therapeutic areas : immunology, oncology, virology and neuroscience.

In more than 75 countries, AbbVie employees are working every day to advance health solutions for people around the world.

For more information about AbbVie, please visit us at

AbbVie : Determined to Make a Difference Updated

People. Passion. Possibilities. Those three simple words mean everything at AbbVie, where patients always come first. So do cutting-

edge science and innovation, which fuel our expanding pipeline as we take on the world's toughest health challenges in oncology, immunology, liver disease, women's health and beyond.

Together, we strive to make a difference for patients around the world. For more visit : www.abbvie.com.

To enable AbbVie’ s emergence as a world class R&D organization, the position anticipates and proactively solves study-related clinical site issues as they occur and initiates, recommends and communicates corrective action ensuring successful protocol level execution of SMM deliverables involving start-

up, execution, and close-out of studies.

  • Appropriate tertiary qualification, health related (e.g., Medical, Scientific, Nursing) preferred.
  • Minimum of 1 year of clinically-related experience, of which a period of 6 months is preferable in clinical research monitoring.
  • Experience in on-site monitoring of investigational drug or device trials is required

  • Current in-depth knowledge and understanding of appropriate therapeutic indications as they relate to the conduct of clinical trials. Delete
  • Current in-depth knowledge of regulations governing clinical research, ICH / GCP Guidelines and applicable regulations
  • Strong planning and organizational skills and the ability to work effectively and efficiently in a dynamic environment with competing projects and deadlines.
  • Ability to work, understand and follow work processes within the assigned function.

  • Strong analytical and conceptual capabilities, interpersonal skills, and ability to communicate with clarity. Ability to address study related clinical site issues with appropriate guidance and initiates and communicate corrective action as indicated.
  • Ability to use functional expertise and exercise good judgment.

  • Demonstrated business ethics and integrity.Travel : 25% travel
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