Statistical Science Lead, Director
Posted Today by Planet Pharma
Negotiable
Undetermined
Hybrid
Addlestone, England, United Kingdom
Summary: The Statistical Director role offers a strategic leadership opportunity within oncology clinical development, focusing on statistical guidance and collaboration in a global pharmaceutical setting. The position involves overseeing complex statistical initiatives, contributing to regulatory submissions, and providing expert support across multiple oncology projects. This role allows for a flexible, home-based work arrangement in the UK with minimal in-office commitments. Candidates will influence the future of cancer treatments through innovative statistical methodologies and collaboration with cross-functional teams.
Key Responsibilities:
- Provide expert statistical support across multiple oncology projects, including Phase I-III trials, biomarker analyses, and regulatory submissions.
- Lead complex study activities, offering strategic input on study design, analysis plans, and methodology, including Bayesian frameworks and survival analysis.
- Collaborate with study teams, medical affairs, and biomarker groups to ensure high-quality, consistent statistical deliverables.
- Represent statistical perspectives in meetings with regulatory authorities and key external stakeholders.
- Contribute to the development and validation of innovative statistical methodologies and train junior statisticians.
- Support the preparation of dossiers, publications, and presentations, translating complex data into actionable insights.
Key Skills:
- PhD or MSc in Biostatistics, Statistics, or related scientific discipline.
- Minimum 6 years (PhD) or 9+ years (MSc) of relevant industry experience, with a strong background in oncology drug development.
- Expertise in advanced statistical methods, including survival analysis and Bayesian approaches.
- Proficiency in SAS; R knowledge is a plus.
- Demonstrated experience supporting regulatory submissions and interacting with regulatory agencies.
- Strong strategic thinking, communication skills, and ability to work independently within cross-functional teams.
- Familiarity with data management processes and international work environments.
Salary (Rate): undetermined
City: Addlestone
Country: United Kingdom
Working Arrangements: hybrid
IR35 Status: undetermined
Seniority Level: undetermined
Industry: Other
Exciting Opportunity: Statistical Director – Drive Innovation in Oncology Clinical Development
Join a pioneering team at the forefront of oncology research and development as a Statistical Director. This strategic leadership role offers the chance to influence the future of cancer treatments through expert statistical guidance and collaboration in a dynamic, global pharmaceutical environment. You will oversee complex statistical initiatives, work with cross-functional teams, and contribute to regulatory submissions, all while maintaining a flexible, home-based work arrangement in the UK with minimal in-office commitments.
What You Will Do
- Provide expert statistical support across multiple oncology projects, including Phase I-III trials, biomarker analyses, and regulatory submissions.
- Lead complex study activities, offering strategic input on study design, analysis plans, and methodology, including Bayesian frameworks and survival analysis.
- Collaborate with study teams, medical affairs, and biomarker groups to ensure high-quality, consistent statistical deliverables.
- Represent statistical perspectives in meetings with regulatory authorities and key external stakeholders.
- Contribute to the development and validation of innovative statistical methodologies and train junior statisticians.
- Support the preparation of dossiers, publications, and presentations, translating complex data into actionable insights.
Required Skills
- PhD or MSc in Biostatistics, Statistics, or related scientific discipline.
- Minimum 6 years (PhD) or 9+ years (MSc) of relevant industry experience, with a strong background in oncology drug development.
- Expertise in advanced statistical methods, including survival analysis and Bayesian approaches.
- Proficiency in SAS; R knowledge is a plus.
- Demonstrated experience supporting regulatory submissions and interacting with regulatory agencies.
- Strong strategic thinking, communication skills, and ability to work independently within cross-functional teams.
- Familiarity with data management processes and international work environments.
Nice To Have Skills
- Experience with PK/PD analyses and biomarker strategies.
- Background in observational studies and clinical research beyond oncology.
- Prior involvement in early-phase (Phase I/II) clinical trials.
- Membership in professional statistical organizations and external collaborations with academic institutions.
Preferred Education And Experience
- A PhD or MSc in a relevant scientific field, complemented by substantial industry experience.
- Proven track record of delivering impactful statistical leadership in a pharmaceutical or biotech setting.
- Experience working on highly complex methodologies and innovative research projects.
Other Requirements
- Willingness to travel as needed for project meetings and stakeholder engagements.
- Based in the UK, with flexibility for one day per quarter in-office meetings.
If you are a strategic thinker with a passion for advancing oncology therapies through cutting-edge statistical science, we invite you to make a meaningful impact with us. Take the next step in your leadership career and apply now to be part of a global organization shaping the future of medicine.