Associate, Study Management II

🔥 18 minutes ago

🇨🇳 China – Remote

⏰ Full Time

🟢 Junior

🟡 Mid-level

✨ Associate

👻 Ghost score 10%

What it means: how likely this posting is sitting open without active hiring.How to read it: 60% or higher means we think this is a ghost. Lower scores are less of a worry.How we score it: age, reposts, open roles vs team size, how fast jobs close, and whether pay is listed.Fine print: an estimate from public data, not a judgment of the company. Real jobs can score high, so treat it as a hint, not a fact.

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AbbVie

WebsiteLinkedInAll Job Openings

10,000+ employees

Founded 2013

🏥 Healthcare

💼 Consulting

🏭 Manufacturing

Healthcare • Consulting • Manufacturing

AbbVie is a global pharmaceutical company that discovers and delivers innovative medicines and solutions to enhance lives. With a focus on addressing the world's toughest health challenges, AbbVie operates in over 175 countries, providing a wide range of products across areas like immunology, oncology, neuroscience, and aesthetics. Committed to scientific innovation, AbbVie invests heavily in research and development, aiming to produce first-in-class medicines. The company also emphasizes workplace diversity, sustainability, and patient support initiatives, ensuring positive impact for both its patients and the broader community.

📋 Description

• Execute one or more elements of clinical studies in compliance with ICH/GCP, global regulations, and AbbVie policies and procedures • Support the Study Project Manager in leading the cross-functional study team • Prepare Clinical Study Team meeting agendas and minutes • Provide regular study-status updates to the cross-functional team and stakeholders and keep the CTMS up to date • Support development of clinical study blueprints/protocols and associated systems and documents, including informed consent forms, eCRFs, IRT, and CSR • Support vendor selection, scope development, management, and oversight in compliance with AbbVie processes and applicable regulations • Generate study-related training for study teams, study sites, and vendors • Proactively identify, resolve, and/or escalate study-related issues • Participate in process improvement initiatives

🎯 Requirements

• Bachelor’s Degree or OUS equivalent degree required, typically in nursing or scientific field • Registered Nurse licensure with Associate’s Degree in Nursing with relevant experience is also acceptable • Two years of Pharma-related/clinical research related experience or professional equivalent desired • Analytical and critical thinking skills • Good communication skills

🏖️ Benefits

• Equal opportunity employer • Committed to operating with integrity, driving innovation, transforming lives and serving the community