Associate Director, Safety Scientist

🕒 April 28

🏄 California, New Jersey, +1 more states – Remote

🏄 California – Remote 🏖️ New Jersey – Remote 🍂 Massachusetts – Remote

💵 $154.3k - $204.3k / year

⏰ Full Time

🟠 Senior

👔 Director

👻 Ghost score 26%

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

• Focus on early development (phase I) and late stage (phase II-III) safety science activities • Work closely with the Safety Science group as part of a matrix team • Conduct safety assessment and safety risk management activities based on ICH standards • Provide safety expertise for assigned developmental and/or marketed products • Lead signal evaluation/safety monitoring activities • Contribute and assist in pharmacovigilance activities including benefit/risk regulatory activities • Analyze and author safety assessment reports • Collaborate with PSLs, scientists, pharmacoepidemiologists, and other cross-functional personnel • Lead preparation and presentation of safety data at safety governance meetings

🎯 Requirements

• PharmD or PhD in a medical field or biological science and 4+ years of experience in pharmacovigilance in an analytical role • RN with 8+ years in pharmacovigilance in an analytical role • MD or internationally recognized equivalent plus accredited residency or comparable post-medical school clinical training relevant to the country of hiring • 4+ years of clinical experience with patients in a relevant therapeutic area specialty • Significant knowledge of general medicine • 2+ years of pharmaceutical/biotechnology industry experience in Safety Science, Clinical Development, or Clinical Research is preferred • US trained physicians must have achieved board eligibility or certification

🏖️ Benefits

• Medical • Dental • Vision • 401(k) • FSA/HSA • Life Insurance • Paid Time Off • Wellness