Associate Clinical Research Manager

🔥 0 minutes ago

🇺🇸 United States – Remote

💵 $105.8k - $140.8k / year

⏰ Full Time

🟡 Mid-level

🧪 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.

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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

• Oversee clinical monitoring activities and CRA team performance • Ensure compliance with ICH-GCP, local regulations, and company SOPs • Allocate CRA resources and assess workloads to meet study deliverables • Ensure CRAs possess the knowledge and skills required for high-quality monitoring • Manage CRA performance and quality indicators • Strengthen site relationships and support trial delivery • Review monitoring quality and resolve compliance issues • Support study and site milestones with cross-functional teams • Execute assessment visits and accompanied visits when required • Identify issues and develop resolution strategies • Contribute to process optimization and manage risk escalation and resolution • Support site audits, inspections, and Site Compliance Visits • Ensure corrective action and follow-up for identified issues • Recruit, hire, onboard, assign tasks, support, evaluate, mentor, and develop team members • Act as a point of contact for issue escalation and feedback • Address personnel issues promptly and fairly

🎯 Requirements

• Bachelor’s degree or higher in a scientific or healthcare discipline • Minimum 5 years of industry experience in the pharmaceutical, CRO, or relevant field • Thorough understanding of the drug development process • Expert knowledge of international standards (ICH-GCP) and health authority requirements • Understanding of all aspects of monitoring and trial execution • Previous experience as a CRA preferred • Excellent interpersonal skills • Strong organizational skills • Effective written and verbal communication skills • Experience in Oncology highly recommended • Proficient in Microsoft Word, Excel, PowerPoint and Outlook • Fluent in written and verbal English • Adaptable to business trips as required • Valid driver’s license in applicable countries

🏖️ Benefits

• Annual bonus plan eligibility for non-commercial roles • Incentive compensation plan eligibility for commercial roles • Discretionary equity awards • Voluntary participation in the Employee Stock Purchase Plan • Medical insurance • Dental insurance • Vision insurance • 401(k) • FSA/HSA • Life insurance • Paid Time Off • Wellness benefits • Professional development opportunities