Clinical Data Science Associate II — Drive Trial Insights

AbbVie Inc.; Chicago (IL); On-site; USD 110,000 - 170,000; Full time

Benefits offered by this job

Paid time off

Medical/dental/vision insurance

401(k)

Job summary

AbbVie Data Science is seeking a data-focused professional to join our best-in-class team responsible for delivering value from clinical trial data. You will support study startup, conduct, and close-out with cross-functional partners and apply data standards to end-to-end data flow.

The role emphasizes regulatory compliance, effective communication, and the ability to influence stakeholders in a fast-paced environment. A Master’s is preferred and 2+ years of related experience is expected.

Qualifications

• Bachelor’s degree required; Master’s degree preferred.
• 2+ years in clinical research, analytics, life sciences or equivalent experience.
• Demonstrated performance as a key contributor to initiatives and advancement of their organization.
• Demonstrated effective communication skills.
• Demonstrated ability to manage multiple priorities in a fast-paced environment.
• Demonstrated leadership and ability to influence without authority.

Responsibilities

• Execute study assignments using understanding of clinical trial concepts and protocol requirements.
• Engage with DSS and cross-functional study teams to execute activities.
• Utilize available technology to support assigned tasks.
• Apply data standards (CDASH/SDTM) in designing interfaces and data flow.
• Support study startup, conduct, and close-out processes.
• Perform data analyses to support operational decision making.
• Contribute to clinical trial application design specifications.
• Rotate through multiple DS roles to develop broad proficiency.
• Ensure compliance with GCPs, ICH guidelines, AbbVie SOPs and quality standards.

Skills

Effective communication

Leadership

Analytical skills

Problem solving

Education

Bachelor’s degree in business, MIS, CS, life sciences or equivalent

Job description

AbbVie Data Science is seeking a data-focused professional to join our best-in-class team responsible for delivering value from clinical trial data. You will support study startup, conduct, and close-out with cross-functional partners and apply data standards to end-to-end data flow.

The role emphasizes regulatory compliance, effective communication, and the ability to influence stakeholders in a fast-paced environment. A Master’s is preferred and 2+ years of related experience is expected.