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

Under direct supervision, supports development of clinical trial application design specifications

May complete rotation through multiple DS roles to establish a base proficiency and to develop a holistic understanding of Data and Statistical Sciences and of clinical development stakeholders

Ensures adherence to federal regulations and applicable local regulations, Good Clinical Practices (GCPs), ICH Guidelines, AbbVie Standard Operating Procedures (SOPs), and to functional quality standards. Stays abreast of new and/or evolving local regulations, guidelines and policies related to clinical development

Bachelor’s degree in business, management information systems, 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

Associate, Clinical Data Systems

Responsibilities

Qualification

Required

Benefits

Company

AbbVie

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