Clinical Data Systems Analyst – Early Career

AbbVie Inc.

North Chicago (IL)

On-site

USD 59,000 - 104,000

Full time

5 days ago
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Job summary

AbbVie Data Science is a best-in-class team responsible for bringing people, process, and technology together to generate business value from clinical trials data. This role supports program- and study-level accountabilities within Data and Statistical Sciences.

Under direct supervision, you will assist with study startup, conduct, and close-out, perform data analyses for operational decisions, and help develop design specifications while ensuring adherence to GCP, ICH guidelines, and AbbVie

Qualifications

  • Bachelor’s degree in business, MIS, computer science, life sciences or equivalent.
  • Demonstrated performance as a key contributor to initiatives and advancement of their organization (academic, internships, or in a previous job).
  • Demonstrated effective communication skills.
  • Demonstrated problem-solving and analytical skills.
  • Demonstrated leadership traits.

Responsibilities

  • Develops a deep understanding of clinical trial concepts and the ability to interpret cross-functional protocol requirements.
  • Engages with DSS and cross-functional study teams to execute assigned activities.
  • Establishes proficiency with available technology to execute activities.
  • Under direct supervision, supports study startup, conduct and close-out processes.
  • Performs data analyses in support of operational decision making.
  • Supports development of clinical trial application design specifications.
  • May rotate through multiple DS roles to build proficiency and understanding.

Skills

Communication skills
Problem solving
Leadership

Education

Bachelor's degree

Job description

AbbVie Data Science is a best-in-class team responsible for bringing people, process, and technology together to generate business value from clinical trials data. This role supports program- and study-level accountabilities within Data and Statistical Sciences.

Under direct supervision, you will assist with study startup, conduct, and close-out, perform data analyses for operational decisions, and help develop design specifications while ensuring adherence to GCP, ICH guidelines, and AbbVie

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