Study Management Associate III

AbbVie

Study Management Associate III managing global clinical trials at AbbVie. Responsible for clinical study leadership and execution while ensuring compliance and quality standards.

Posted 7/3/2026full-timeRemote • 🇲🇽 MexicoJuniorMid-LevelWebsite

Tech Stack

Tools & technologies

Google Cloud Platform

About the role

Key responsibilities & impact

Work independently as a clinical study leader and contributor
Support the Study Project Manager in strategic leadership of the cross-functional team
Manage vendor relationships and oversight of external vendors
Oversee recruitment management and execution of recruitment strategies
Ensure inspection readiness and participate in related activities
Manage study materials and ensure compliance/inspection readiness

Requirements

What you’ll need

Bachelor’s Degree
At least 4 years of progressive Pharma-related/clinical research-related experience
Competent in application of standard quality procedures (SOP, ICH/GCP, Global Regulations)
Experienced user of systems such as EDC, IRT, CTMS, and eTMF
Strong analytical and critical thinking skills
Excellent organizational and time management skills
Exceptional interpersonal skills with ability to communicate effectively in English

Benefits

Comp & perks

Health insurance
Flexible work arrangements

ATS Keywords

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Applicant Tracking System Keywords

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Hard Skills & Tools

Pharma-Related ExperienceClinical Research ExperienceStandard Quality ProceduresSOP ApplicationICH/GCP Knowledge

Soft Skills

Organizational SkillsTime ManagementInterpersonal SkillsEffective Communication