Associate Study Management III

🔥 1 minute ago

🇨🇳 China – Remote

⏰ Full Time

🟡 Mid-level

✨ Associate

👻 Ghost score 10%

What it means: the chance that no one is really hiring for this job.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.

Apply Now

Find Similar Remote Jobs

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

• Provide study-level oversight and leadership for one or more global clinical trials from inception through closure • Support the Study Project Manager in strategic leadership of cross-functional teams, stakeholder engagement, strategy development, meeting facilitation, documentation, deliverables, and timelines • Manage external vendors, including RFPs, selection, scope of work, deliverable oversight, and risk management • Lead global recruitment management, strategy development, and mitigation planning from country feasibility through subject recruitment and retention • Lead cross-functional, vendor, and investigator meetings; prepare agendas, curate and file minutes, and provide study-status updates • Ensure inspection readiness and participate in related activities • Identify, mitigate, escalate, and manage risks and issues; support trend analysis and risk prevention • Co-develop and manage study materials, including protocols, regulatory submissions, patient-reported outcome measures, study execution plans, informed consent, site budgets and agreements, clinical study reports, training materials, newsletters, and stakeholder presentations • Manage CTMS and eTMF to support compliance, inspection readiness, trend analysis, and timelines • Support EDC, IRT, and ePRO design reviews, user acceptance testing, plans, key risk indicators, access support, query resolution, and system oversight • Manage investigational product and associated study supplies • Provide training to study team members, vendors, and other stakeholders • Support global submission strategies • Support process improvement initiatives or serve as a subject matter expert and/or mentor

🎯 Requirements

• Bachelor’s Degree or OUS equivalent required • At least 4 years of progressive Pharma-related/clinical research-related experience with a high level of core and technical competencies • Competent in application of standard quality procedures (SOP, ICH/GCP, Global Regulations) • Experienced user of EDC, IRT, CTMS, and eTMF • Strong analytical and critical thinking skills to evaluate complex issues from multiple perspectives and develop strategies • Excellent organizational and time management skills; strong attention to detail • Exceptional interpersonal skills and ability to communicate effectively in a clear and persuasive manner in a global setting • Proficient in business/technical English-language (oral and written) • Proactive, collaborative mindset • Ability to work independently in a fast-paced global team environment • Preferred: exposure to study initiation through completion activities; global study exposure

📊 Check your resume score for this job

Improve your chances of getting an interview by checking your resume score before you apply.

Upload Resume