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AbbVie Inc.: Associate, Study Management II//CTM II

Observed on the employer’s careers system, last checked 2026-09-09.

POSTED: 2026-09-09Listed

Cite: FACTANKER, https://factanker.com/jobs/posting/6dc69eda-78c7-4cf1-9136-ea58bb2b7a37

Employer
AbbVie Inc.
Location
Shanghai
Category
Research
Posted
2026-09-09
Careers system
smartrecruiters
Observed
2026-09-09

Apply on the employer’s site ↗

Role description

Verbatim from the employer’s posting, rendered as plain text.

•Responsible for executing one or more elements of clinical studies in compliance with quality standards (ICH/GCP, Global Regulations, and AbbVie policies and procedures). •Supports the Study Project Manager in leading the cross functional study team: o -Supports the preparation of Clinical Study Team meetings (Agenda/Minutes) o -Responsible for regular updates to the cross-functional team and stakeholders on study status; ensure our CTMS is up to date •Supports the development of the clinical study blueprint/protocol and associated systems and documents (Informed consent forms, eCRFs, IRT, CSR) Supports the vendor selection, scope development, management and oversight of external vendors in compliance with AbbVie’s processes and procedures and the applicable regulations. •Responsible for generating the study related training for the study team, study sites, and vendors for assigned…

Provenance

Official posting
https://jobs.smartrecruiters.com/AbbVie/3743990015129666
Retrieved
2026-09-13 08:45:00.598816+02:00
ATS reference
3743990015129666