Clinical Operations Manager

🔥 1 minute ago

🇨🇳 China – Remote

⏰ Full Time

🟡 Mid-level

🟠 Senior

🏥 Clinical Operations

👻 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

• Manage day-to-day monitoring activities on assigned studies to ensure deliverables are met • Track and maintain project metrics and deliverable status • Communicate and escalate issues, risks, and staffing needs to Program Leads, RSMs, and the Clinical Trial Team • Answer study questions and provide guidance as Allergan standard study process experts • Review Site Feasibility Questionnaires and Site Qualification Visit reports • Maintain tracking reports for SIV, IMV, RMV, and COV • Develop monitoring documents and toolkits, including Protocol Specific Monitoring Plans, amendments, report annotation, visit checklists, and toolkits • Provide PSMP training and assist with GSMO orientation sessions • Conduct teleconferences with RSMs to deliver training and information • Attend team meetings and disseminate information • Collaborate with CTT and GSMO PL on study-specific eCRFs, completion guidelines, protocol deviation specifications, and user acceptance testing • Serve as a Risk Based Monitoring ambassador and ensure RBM implementation and adherence • Maintain the monitoring portion of the study portal • Maintain knowledge of ICH/GCP, regulatory requirements, Allergan SOPs, and therapeutic-area protocols and amendments • Monitor or co-monitor/oversee assigned trial sites • Mentor new LSMs and assist with LSM orientation training • Contribute to process development, improvement, and documentation to drive consistency • Train RSMs on trial specifics

🎯 Requirements

• Allied Health Professions degree (PA, RN, RPh), relevant clinical experience, or four-year life science degree • Minimum 5 years monitoring experience in a pharmaceutical or medical device company or clinical research organization • More than 5 years of industry experience • Prefer candidates that have functioned as a lead monitor or have equivalent experience • Advanced skills in Microsoft Word, Microsoft PowerPoint, Microsoft Excel, and Microsoft OneNote • Excellent written and oral communication skills • Planning, organizing, metrics tracking, controlling, directing, and promoting innovation • Decision making, judgment, and problem solving • People relationships, influencing others, motivating employees, team building, and developing people • Initiative and accountability • Assigning work, reviewing work, and planning others' work • Maintaining and coordinating activities • Ability to train RSMs on trial specifics

🏖️ Benefits

• Equal opportunity employer • Operating with integrity, driving innovation, transforming lives and serving the community