Associate, Clinical Data Systems

Regulatory Jobs; Florham Park (NJ); On-site; USD 110,000 - 150,000; Full time

Job summary

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

Responsibilities include understanding trial concepts, engaging with study teams, leveraging technology, and assisting with startup, conduct, and close-out processes under supervision. Data analyses support operational decisions.

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 assigned activities.
• Establishes proficiency with available technology to execute assigned activities.
• Supports the execution of processes in study startup, conduct and close-out under direct supervision.
• Performs data analyses in support of operational decision support under direct supervision.

Job description

About AbbVie

AbbVie's mission is to discover and deliver innovative medicines and solutions that solve serious health issues today and address the medical challenges of tomorrow. We strive to have a remarkable impact on people's lives across several key therapeutic areas including immunology, oncology and neuroscience - and products and services in our Allergan Aesthetics portfolio. For more information about AbbVie, please visit us at www.abbvie.com.

AbbVie Data Science is the best-in-class team within its cross-industry peer group and is responsible for bringing people, process, and technology together to generate business value from clinical trials data. Our operational model is exemplified through execution and innovation. This role is key to ensuring successful delivery against the program- and study-level accountabilities assigned to Data and Statistical Sciences.

Responsibilities:

• Develops a deep understanding of clinical trial concepts and the ability to effectively interpret cross-functional protocol requirements
• Engages with members of the DSS and cross-functional study teams in order to effectively execute assigned activities
• Establishes proficiency with and effectively utilizes available technology to execute assigned activities
• Establishes proficiency with standards to be used in the design and development of key system interfaces
• Under direct supervision, supports the execution of all processes in support of study startup, conduct and close-out
• Under direct supervision, performs data analyses in support of operational decision support