Senior Global Clinical Study Manager

🕒 August 14

🇺🇸 United States – Remote

💵 $136.4k - $181.4k / year

⏰ Full Time

🟠 Senior

🧪 Clinical Research

👻 Ghost score 1%

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.

Apply Now

Find Similar Remote Jobs

Set Up Email Alert For New Jobs

📊 Check your resume score for this job

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

Upload Resume

BeOne Medicines

WebsiteLinkedInAll Job Openings

10,000+ employees

Founded 2010

🧬 Biotechnology

🏥 Healthcare

💊 Pharmaceuticals

Biotechnology • Healthcare • Pharmaceuticals

BeOne Medicines is a global oncology company domiciled in Switzerland that is discovering and developing innovative treatments that are more affordable and accessible to cancer patients worldwide. With a portfolio spanning hematology and solid tumors, BeOne is expediting the development of its diverse pipeline of novel therapeutics through its internal capabilities and collaborations. With a growing global team of more than 11,000 colleagues spanning six continents, the Company is committed to radically improving access to medicines for far more patients who need them.

📋 Description

• Own global study delivery within agreed timelines, budget, quality, and inspection-readiness requirements for Clinical SuperHighway partnership studies • Lead all aspects of assigned clinical studies from feasibility through closeout • Lead global cross-functional study teams and oversee external partners and vendors • Act as escalation point for study-related issues and keep senior management informed of progress, risks, and challenges • Plan and manage study timelines, feasibility, site selection, startup, site activation, submissions, and closeout activities • Ensure study plans, systems, tools, training, and Trial Master Files are created, maintained, QC’d, and implemented appropriately • Implement risk-based quality management processes and monitor study compliance with protocols, SOPs, ICH/GCP, and regulations • Prepare teams for quality assurance audits and inspections and ensure ongoing inspection readiness • Coordinate supplies forecasting and delivery, data cleaning timelines, and Clinical Study Report planning • Manage study vendors, budgets, invoices, accruals, forecasts, and resource needs • Contribute to process improvements and develop or optimize work instructions and SOPs

🎯 Requirements

• Proven project management experience in global clinical studies • Oncology experience preferred • Advanced knowledge of clinical operations methodologies • In-depth understanding of all aspects of clinical study processes • Ability to independently lead global clinical studies • 8 or more years of progressive clinical research experience within biotech, pharma, or CRO industry • Bachelor’s degree in a scientific or healthcare discipline required; exceptions may be made for candidates with relevant clinical operations experience • Higher degree preferred • Proficiency with MS Office, project planning applications, and Clinical Trial Management Systems (CTMS)

🏖️ Benefits

• Annual bonus plan eligibility for Non-Commercial roles • Discretionary equity awards • Employee Stock Purchase Plan • Medical insurance • Dental insurance • Vision insurance • 401(k) • FSA/HSA • Life insurance • Paid Time Off • Wellness program