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Job Opportunity: Global Statistical Lead in Oncology
We are currently supporting a leading global biopharmaceutical company in their search for an experienced Global Statistical Lead with a strong background in oncology drug development. This is a high-impact individual contributor role offering the opportunity to provide strategic input across clinical development, focusing on Phase I–III oncology studies.
Key Responsibilities:
* Provide strategic statistical leadership to support clinical development plans, focusing on oncology and immuno-oncology programs.
* Lead and coordinate all statistical activities across multiple functions (e.g., Clinical Development, Biomarkers, Medical Affairs).
* Collaborate with and guide study-level statisticians, ensuring quality and consistency across trials.
* Support submissions and regulatory strategies, including participating in key interactions with health authorities.
* Influence cross-functional decision-making by working closely with Clinical, Regulatory, and other stakeholders.
* Apply advanced statistical methodologies, including Bayesian frameworks and survival analysis, to support data-driven decisions.
Key Requirements:
* PhD with at least 9 years, or Master’s degree with at least 12 years of relevant experience in the pharmaceutical or biotech industry.
* Strong expertise in oncology clinical trials, especially in Phase I–III studies.
* Proven experience in statistical strategy, including input to clinical development plans and submission activities.
* Ability to lead cross-functional teams and influence key decisions without direct line management responsibility.
* Proficiency in survival analysis; familiarity with Bayesian methods is highly desirable.
If interested, please click ‘apply’ or contact David Rowland (Recruiter II) at Planet Pharma for more information.
Planet Pharma is an American-based employment agency providing global staffing services. With headquarters in Chicago and an EMEA regional office in Central London, we operate in over 30 countries with a network of 2500+ active contractors globally. We offer extensive expertise in regulatory affairs, pharmacovigilance, QA, QC, submissions, clinical development, biostatistics, and medical affairs/writing.
We are an equal opportunity employer and welcome applications from all qualified candidates regardless of race, sex, disability, religion, sexual orientation, or age.
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