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Dragonfly Therapeutics
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Apellis Pharmaceuticals
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Associate Director, Biostatistics
$132k-170k (estimate)
Full Time | Scientific Services 2 Days Ago
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Dragonfly Therapeutics is Hiring an Associate Director, Biostatistics Near Waltham, MA


Dragonfly Therapeutics seeks an Associate Director, Biostatistics to lead, develop, and implement statistical analyses to support our early development clinical trials, and provide support to investigators and researchers on experimental design and statistical approaches, requirements, and scientific standards. This role will report to the Head of Biometrics, is hands-on and requires excellent communication skills and frequent collaboration with multiple internal groups. The successful candidate can work independently and thrives in a proactive can-do culture. The work will be fast-paced with evolving needs, requiring adaptability, curiosity, and grace under pressure. This role is an exciting opportunity to be a critical part of the clinical development group, involved in the design, execution, analysis, and reporting of Dragonfly's clinical studies.
Responsibilities:
  • Serve as the biostatistician in the Clinical Operations and Development team, responsible for all clinical study biostatistics deliverables
  • Analyze and interpret data from various sources, using standard statistical analysis software to perform appropriate statistical analyses on clinical trial patient data
  • Develop statistical sections of protocols and statistical analysis plans and assist in the preparation of clinical trial documents and reports, protocols, investigator brochures, scientific abstracts, peer-reviewed manuscripts, and responses from regulatory agencies
  • Make recommendations on appropriate study design, methodology, analytic and operational approach, sample size and power considerations
  • Ensure that clinical trials meet statistical requirements (ICH, FDA, EMA guidelines) and are conducted with appropriate rigor
  • Provide ongoing reporting of clinical trial data as needed
  • Perform exploratory data analyses on patient subgroups
  • Collaborate with translational science and pharmacokinetic colleagues as needed to analyze early phase trial data
  • Maintain knowledge of current and emerging trends in state-of-the-art statistical and analytic techniques
  • Collaborate with, and manage internal and external functions (e.g. CROs, software vendors, clinical development partners, etc.) to meet project timelines and achieve goals
  • Collaborate with cross-functional team to review study results and contribute scientific knowledge and analytical skills to the production of documents
Qualifications
  • Ph.D. in statistics (or closely related field e.g. medical statistics, biometrics, medical informatics, biopharmaceutical statistics) with 6 years biopharmaceutical industry experience as a biostatistician or a Master's degree in a relevant statistics field and 8 years industry experience (as a biostatistician) in Biotech, Pharma, Regulatory agencies, or Clinical Research Organizations
  • Ability to analyze, interpret, and summarize clinical and scientific data using a range of advanced statistical techniques for statistical analyses
  • Skill in preparing graphical data displays
  • Knowledge of scientific approach and methodologies as well as principles, concepts, methods, and standards of statistical research
  • Solid understanding of drug development, clinical research, study design, pharmacokinetics, and medical terminology
  • Experience with CRO vendor oversight is preferred
  • Experience in oncology and oncology statistical methods used is preferred
  • Working knowledge of data management principles and regulatory requirements for clinical trials and medical research, including relevant ICH guidelines, US, EU and other regions' regulations
  • Strong organizational and analytical skills, with the ability to be proactive, think strategically and manage multiple projects simultaneously
  • Ability to interact effectively with team members, proactively facilitating effective information exchange, with strong communication and problem-solving skills
About DragonflyDragonfly Therapeutics is a clinical-stage biopharmaceutical company committed to discovering, developing and commercializing therapies that use its novel multispecific antibody technology to harness the body's immune system to bring breakthrough treatments to patients. In addition to its wholly owned clinical assets, Dragonfly has a deep pipeline of wholly owned preclinical candidates discovered using its proprietary platform, as well as productive collaborations with Merck, AbbVie, Gilead and Bristol Myers Squibb in a broad range of disease areas.
Our mission is to revolutionize disease treatment by inventing natural killer cell-based therapies for vastly improved patient outcomes. We believe in a small team with a big impact.

Job Summary

JOB TYPE

Full Time

INDUSTRY

Scientific Services

SALARY

$132k-170k (estimate)

POST DATE

06/01/2024

EXPIRATION DATE

06/19/2024

WEBSITE

dragonflytx.com

HEADQUARTERS

CAMBRIDGE, MA

SIZE

100 - 200

FOUNDED

2015

CEO

BILL HANEY

REVENUE

<$5M

INDUSTRY

Scientific Services

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The following is the career advancement route for Associate Director, Biostatistics positions, which can be used as a reference in future career path planning. As an Associate Director, Biostatistics, it can be promoted into senior positions as a Top Clinical Information Systems Executive that are expected to handle more key tasks, people in this role will get a higher salary paid than an ordinary Associate Director, Biostatistics. You can explore the career advancement for an Associate Director, Biostatistics below and select your interested title to get hiring information.

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