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NuvalentNU

Senior Director, Biostatistics - Oncology

Nuvalent is a clinical-stage biopharmaceutical company focused on creating precisely targeted therapies for patients with cancer, designed to overcome the limitations of existing therapies for clinically proven kinase targets.

Nuvalent

Employee count: 51-200

Salary: 265k-300k USD

United States only

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The Company:With deep expertise in chemistry, Nuvalent is working to create selective medicines designed with the goal to address the needs of patients with cancer. Nuvalent is an exciting early-stage company, bringing together experienced scientists and industry veterans with a proven track record in drug discovery, oncology drug development, and company building.

The Role:

Reporting to the Vice President, Biostatistics, the Senior Biostatistics will serve as the project lead statistician responsible for statistical activities at study level and compound level, including, protocol development, study design, statistical data analysis, regulatory submissions, publications, and presentations at Nuvalent. The Senior Director, Statistics will also oversee CRO statistics deliverables for all Nuvalent studies.

Responsibilities:

  • Lead the development of statistical sections of clinical study protocols, statistical analysis plans, and conduct the analysis and reporting of clinical trial data
  • Provide strategic input to optimize trial designs in early phase dose escalation studies and late phase registrational studies
  • Oversee CRO statistical activities and manage contractor statisticians to ensure timely delivery of high-quality statistical outputs
  • As the biostatistics representative, proactively collaborate with internal and external team members in the assigned projects, accountable for all statistics deliverables
  • Contribute to the biostatistics vendor evaluation and selection
  • Provide a thorough review for required components of regulatory submissions including appropriate datasets, define files, reviewer's guides, and other relevant documents
  • Contribute to the development of Biostatistics SOPs and standards
  • Support study/program-level audit and inspection readiness activities as needed
  • Develop and maintain advanced competencies in statistical methodology and advanced trials designs, particularly in oncology drug development

Competencies:

  • Adaptability/Flexibility – The ability to adapt to working effectively within a variety of situations; adapts enthusiastically to organizational change and to changes in job demands.
  • Communication and Teamwork – Ability to effectively express ideas in written and oral context; to work co-operatively with others; genuine desire to be a part of a team and contribute to organizational and team goals.
  • Effective Planning – Embed discipline and thoroughness in our approaches.
  • Perseverance – Pursues tasks with energy, drive, and initiative, even in the face of adversity; comfortable in a results-driven, highly accountable environment where you can make an impact.
  • Problem Solving – Ability to understand a situation or problem by breaking it down into smaller pieces using a systematic approach and to identify patterns and connections between situations that are not obviously related.
  • Relationship Building – Builds productive working relationships across a diverse spectrum of people.
  • Organizational Skills – Ability to handle multiple responsibilities simultaneously and still meet high quality and timeliness standards under pressure.

Qualifications:

  • Minimum of MS required (Ph.D. preferred) in Statistics, Biostatistics, or other related fields
  • MS with 12+ years (Ph.D. with 8+ years) of overall experience, including at least 10+ years (at least 6+ years for Ph.D.) of experience in drug development in a CRO or pharma/biotech company
  • Oncology experience is strongly preferred: familiar with oncology drug development, both early and late stage, including efficacy endpoints, RECIST criteria, common statistical issues and study designs in oncology
  • Regulatory NDA/BLA submission experience is strongly preferred
  • Must have hands on experiences with SAS programming in clinical studies
  • Experience with managing CROs and contractors
  • Excitement about the vision and mission of Nuvalent and working on drug development
  • Excellent project management skills and proven ability to manage competing priorities

Additional Information:

Nuvalent is committed to fair and equitable compensation practices, aiming to provide employees with market-competitive total rewards packages. .

The targeted salary range below reflects what Nuvalent reasonably and in good faith expects to offer for this position at the time of posting, but the final salary determination may be within or outside this range based on various factors, including, but not limited to, experience, skills, education, and market factors. The range will be reviewed regularly and is subject to change.

Nuvalent also offers a comprehensive benefit package to support our employees at each stage of their career, financial, health, and well-being journey, including medical, dental, and vision insurance, 401(k) retirement savings plan, generous paid time off (including a summer and winter company shutdown), and much more.

Annual Salary Range
$265,000—$300,000 USD

Nuvalent provides equal employment opportunities (EEO) to all employees and applicants for employment without regard to religion, race, creed, color, sex, sexual orientation, alienage or citizenship status, national origin, age, marital status, pregnancy, disability, veteran or military status, predisposing genetic characteristics or any other characteristic protected by applicable federal, state or local law.


Nuvalent is aware that many companies are dealing with fraudulent job postings on third-party employment search sites and/or individual(s) or entities claiming to be employees of such companies. Those involved are offering fraudulent employment opportunities to applicants, often asking for sensitive personal and financial information, and using such information for criminal activities.

Please be advised that all legitimate correspondence from a Nuvalent employee will come from "@nuvalent.com" email accounts. Automated system response emails from our Greenhouse applicant tracking system come from a “no-reply@greenhouse.io” email address. There are no variations of these email addresses and Nuvalent would not request personal and/or financial information via email. Job opportunities would only be extended after a completed job application is submitted by a candidate and a thorough interview process including 1:1 and/or group interviews via phone, video conferencing and/or in-person.

If you believe you have been contacted by anyone misrepresenting themselves as an employee of Nuvalent, please contact Nuvalent at 857-357-7000. Thank you.

About the job

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Job type

Full Time

Experience level

Director
Executive

Salary

Salary: 265k-300k USD

Location requirements

Hiring timezones

United States +/- 0 hours

About Nuvalent

Learn more about Nuvalent and their company culture.

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At Nuvalent, Inc., we are at the forefront of oncological innovation, dedicated to creating precisely targeted therapies that address the significant unmet needs of cancer patients. Leveraging our deep expertise in chemistry and state-of-the-art structure-based drug design, we are revolutionizing the development of novel small molecules. Our innovative approach focuses on engineering therapies with exquisite target selectivity, a critical factor in overcoming drug resistance, minimizing adverse events often associated with less targeted treatments, and effectively addressing brain metastases, a common and challenging complication in many cancers. We believe this precision is key to driving more durable and meaningful responses for patients, ultimately transforming their treatment journeys and outcomes.

Our robust pipeline features parallel lead programs targeting ROS1-positive and ALK-positive non-small cell lung cancer (NSCLC), two areas where existing therapies have limitations. Beyond these advanced programs, Nuvalent is actively pursuing multiple discovery-stage research initiatives, continually seeking new clinically proven kinase targets. This relentless pursuit of scientific advancement underscores our commitment to expanding the frontiers of cancer treatment. Our team, comprised of experienced scientists and industry veterans, is driven by a shared passion for patient impact, empowerment, and collaboration. These core values guide our daily work as we strive to translate groundbreaking scientific insights into tangible therapeutic options that can make a profound difference in the lives of those affected by cancer. We are committed to not only advancing our current programs but also to fostering a culture of continuous innovation to tackle the evolving challenges in oncology.

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Nuvalent hiring Senior Director, Biostatistics - Oncology • Remote (Work from Home) | Himalayas