Feasibility Associate

🔥 13 hours ago

🇺🇸 United States – Remote

💵 $76.2k - $101.2k / year

⏰ Full Time

🟢 Junior

🟡 Mid-level

🚫👨‍🎓 No degree required

👻 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

• Maintain detailed records of work and internal libraries and databases • Remain informed of current scientific and clinical research • Support cross-functional meetings and prepare meeting materials • Resolve feasibility issues during clinical-trial site selection • Optimize feasibility-related data resources and materials • Participate in country and/or site feasibility activities for regional and country clinical trials • Mine internal databases and review investigators for quality assurance • Develop prioritized site lists based on historic site performance and capability • Reconcile and interpret feasibility data and provide country-level assessments • Coordinate collection and delivery of feasibility data with internal and external customers • Review and update site-list information • Conduct CDA outreach and execute required feasibility documents • Serve as primary feasibility contact for assigned studies • Manage feasibility outreach and investigator engagement to assess study interest and site capabilities • Collaborate with Clinical Operations, Site Management, Data Sciences, Medical Affairs, and external partners • Participate in study kickoff, feasibility strategy, and enrollment planning meetings • Support process-improvement initiatives and enhance feasibility methodologies, templates, and data resources • Support onboarding and training activities • Contribute to standardized processes, training materials, and operational efficiencies

🎯 Requirements

• Bachelor’s degree or higher in a scientific or healthcare discipline preferred • Minimum of 2 years of progressive experience in clinical research and clinical operations • Experience preferably within the biotech, pharmaceutical sector, CRO, or clinical site environment • Microsoft Office Suite • CTMS applications • EDC applications • Analytic tools such as Citeline and Trialtrove • Additional feasibility software • Travel might be required as per business need

🏖️ Benefits

• Annual bonus plan for non-commercial roles • Incentive compensation plan for 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 benefits • Reasonable accommodation for applicants with disabilities