Clinical Data Systems Associate — Trial Data Insights

AbbVie Inc.; Florham Park (NJ); On-site; USD 5,900 - 104,000; Full time

Job summary

AbbVie Data Science is seeking a capable professional to join the team in New Jersey. You will support study startup through close-out, analyze data for operational decisions, and collaborate with cross-functional study teams to interpret trial concepts and requirements.

The role emphasizes learning, adherence to GCP/ICH and AbbVie SOPs, and developing design specifications for clinical trial applications under supervision.

Qualifications

• Bachelor’s degree in specified fields or equivalent.
• Experience as a key contributor in projects or internships.
• Strong communication and analytical skills.
• Demonstrated leadership traits and ability to work cross-functionally.

Responsibilities

• Develops a deep understanding of clinical trial concepts and ability to interpret cross-functional protocol requirements.
• Engages with DSS and cross-functional study teams to execute activities.
• Establishes proficiency with technology to execute assigned activities.
• Establishes proficiency with standards for the design and development of key system interfaces.
• Under direct supervision, supports the execution of all processes in study startup, conduct and close-out.
• Under direct supervision, performs data analyses in support of operational decision support.
• Under direct supervision, supports development of clinical trial application design specifications.
• May complete rotation through multiple DS roles to build a holistic understanding for stakeholders.

Skills

Communication skills

Problem-solving

Leadership traits

Team collaboration

Education

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

Job description

AbbVie Data Science is seeking a capable professional to join the team in New Jersey. You will support study startup through close-out, analyze data for operational decisions, and collaborate with cross-functional study teams to interpret trial concepts and requirements.

The role emphasizes learning, adherence to GCP/ICH and AbbVie SOPs, and developing design specifications for clinical trial applications under supervision.