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About AbbVie

AbbVie (NYSE:ABBV) 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 www.abbvie.com. Follow @abbvie on Twitter, Facebook or LinkedIn.​

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Research & Development
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1902098 Requisition #
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The Translational Oncology group at Abbvie uses advanced methods to discover biomarkers and implement Translational Medicine strategies to progress AbbVie’s innovative Oncology pipeline. We are currently seeking highly motivated individuals to join our Biomarker Program Management team to support the implementation of Translational Medicine strategies.  As a member of project teams, he/she will have the opportunity to work in a highly collaborative environment to support projects across all phases of clinical development. 


Key Responsibilities Include:

  • Provide hands-on support for operationalizing biomarker research in clinical trial, including sample and data management, and CRO management.
  • Author the Translational sections in key clinical documents including Protocols, Informed Consent Forms, Contracts, and Clinical Study Reports.
  • Use multiple technologies to maintain open and frequent communication with various AbbVie functions such as Site Management & Monitoring and Clinical Operations. Maintain a positive working relationship with internal/external customers. May assist CRA in training sites on sample collection/handling. 
  • Adhere to applicable country regulations, legal requirements, Good Clinical Practices (GCPs), ICH Guidelines, AbbVie Standard Operating Procedures (SOPs).

Level and compensation will be commensurate with experience.


Basic Qualifications:

  • Master’s Degree in a scientific discipline with 6+ years of related work experience.
  • Bachelor’s Degree in a scientific discipline with 8+ years of related work experience.

Preferred Qualifications:            

  •  Proficient in the conduct of clinical trials and associated activities and responsibilities, as well as experience interacting with clinical trial teams; strong background in oncology a plus.
  • Previous experience with Clinical Biomarker Operations.
  • Proven strong planning and organizational skills and the ability to work effectively and efficiently in a dynamic environment with multiple high priority competing projects and deadlines.
  • Excellent communication and interpersonal skills, including problem solving, crisis management, change management, and conflict resolution. Proactive and positive team player.
  • Able to work in a cross-functional team environment, interacting with various levels within the organization as well as vendors/academic sites/KOLs.
  • Possesses strong oral and written communication skills; proven ability to successfully negotiate with and influence stakeholders with tact and diplomacy.
  • Proficient knowledge of all standard IT office tools; knowledge of LIMS systems a plus.
  • Understanding of Translational Sciences and Companion Diagnostic development is a plus.
  • Project Management experience a plus.                                                                             

Key Leadership Competencies:

  • Ability to operate independently and learn quickly.
  • Possesses strong interpersonal skills/emotional intelligence.
  • Builds strong relationships with peers and cross functionally with partners outside of team to enable higher performance.
  • Raises the bar and is never satisfied with the status quo.
  • Embraces the ideas of others and nurtures innovation

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