Director, CDx Development

🕒 July 15

🇺🇸 United States – Remote

💵 $176.6k - $236.6k / year

⏰ Full Time

🔴 Lead

👔 Director

👻 Ghost score 2%

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

• Lead the development and execution of integrated CDx strategies across clinical development programs, ensuring alignment with overall drug development objectives and timelines. • Engage early with Translational Discovery and Research teams to understand predictive hypotheses and biomarker strategies for pipeline programs. • Partner with internal research teams and external vendors to develop predictive assays when suitable assays are not already available. • Define and advance CDx strategies through internal governance bodies, securing timely alignment and endorsement. • Collaborate cross‑functionally to define Diagnostic Target Product Profiles and identify optimal diagnostic platforms and CDx partners. • Work closely with Regulatory Affairs to support the preparation and submission of regulatory documentation (e.g., IDEs, PMAs) and to interact with global health authorities as needed. • Oversee CDx development activities to ensure on‑time delivery of diagnostic kits to support pharmaceutical registration and commercial launch. • Provide clear, proactive communication to cross‑functional stakeholders on CDx program progress, risks, and mitigation strategies. • Monitor and interpret emerging industry trends, technology advancements, and evolving regulatory requirements related to IVDs and companion diagnostics.

🎯 Requirements

• PhD with a minimum of 5+ years of industry experience in clinical biomarker testing and companion diagnostics development • Strong scientific and technical expertise in clinical development, biomarker strategies, and regulatory requirements for IVD and CDx products • Hands-on knowledge of diagnostic platforms such as NGS, IHC, FISH, and related technologies • Proven ability to lead complex, cross-functional programs to completion on time and within budget • Strong analytical and strategic thinking skills, with the ability to make data-driven decisions in ambiguous or complex situations and to think at a portfolio level • Demonstrated ability to influence and align stakeholders across development and commercial organizations without direct authority • Excellent communication skills, with the ability to convey complex scientific and strategic concepts clearly to both technical and non-technical audiences • Experience working effectively in a matrixed environment and leading cross-functional teams.

🏖️ Benefits

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