Associate Director – Clinical Development

🔥 13 hours ago

🇺🇸 United States – Remote

💵 $208.2k - $258.2k / year

⏰ Full Time

🟠 Senior

👨‍⚕️ Medical Director

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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

• Support BeOne Clinical and Medical assets through execution of clinical development programs and deliverables • Jointly develop clinical program strategy and ensure activities are executed within scope, budget, and timelines • Help establish and grow Clinical Research functions and global capabilities • Collaborate with clinical development, program leadership, biometrics, clinical operations, safety/pharmacovigilance, regulatory, molecular diagnostics, and translational research teams • Facilitate generation, authorship, updating, and review of protocols, informed consent documents, Investigator Brochures, clinical study reports, abstracts, posters, manuscripts, regulatory submissions, risk/benefit analyses, and Clinical Development Plans • Partner with clinical operations and other functions to implement and execute clinical studies • Provide scientific expertise for investigator and vendor selection • Train colleagues, CRO staff, and study site staff on therapeutic areas, molecules, and clinical protocols • Provide scientific and medical support during clinical trials and respond to questions from sites, IRBs/IECs, Health Authorities, and CROs • Review, query, analyze, interpret, and present clinical trial data • Represent clinical studies or development programs on teams and subteams • Create clinical study and program-related slide decks • Build and maintain opinion leader and investigator networks; organize and present at advisory boards and investigator meetings • Conduct therapeutic area/indication research and competitor analysis • Build relationships with internal experts • Identify process improvement opportunities and organizational resource needs • Develop, track, execute, and report on goals and objectives • Support budget planning and management • Ensure compliant business practices

🎯 Requirements

• MD, DO, PhD, PharmD or equivalent international degree required • 4+ years of clinical research experience within biotech/pharma or an equivalent academic environment • Clinical oncology experience; candidates with exceptional experience in other therapeutic areas may be considered if they demonstrate potential to apply their skills to oncology • High level of written and verbal communication, interpersonal, organizational, and cross-functional collaboration skills • Knowledge of GCP and ICH Guidelines • Flexibility to work with colleagues in a global setting • Experience with development and support of related SOPs and policies • Proficiency in Microsoft Word, Excel, and Outlook • Approximately 15% work-related travel

🏖️ Benefits

• Annual bonus plan eligibility for non-commercial roles • Incentive compensation plan eligibility 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

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