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Director Biostatistics

The Gerontological Society of America (GSA).

East Hanover (NJ)

On-site

USD 185,000 - 345,000

Full time

Yesterday
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Job summary

The Gerontological Society of America is seeking a Director of Biostatistics to provide strategic leadership in drug development across multiple therapeutic areas. This role includes collaboration with clinical and regulatory teams, driving statistical strategy, and overseeing project management ensuring high-quality deliverables.

Benefits

401(k) eligibility
Various paid time off benefits
Sign-on bonus potential
Discretionary awards

Qualifications

  • 12+ years relevant work experience for MS or 8+ years for PhD.
  • Advanced knowledge of applying statistics and innovative approaches.
  • Record of successful implementation in drug development.

Responsibilities

  • Influence statistical strategy in drug development.
  • Lead collaborations for quantitative decision-making.
  • Optimize drug development process through innovative designs.

Skills

Biostatistics
Statistical Analysis
Decision Making Skills
Clinical Trials
Data Analytics

Education

MS in Statistics
PhD in Statistics

Tools

Computer Programming

Job description

Job Description Summary
As the Director Biostatistics, you will influence and drives statistical strategy/innovation directly taking part in cross-functional collaboration and decision making for program(s) across multiple indications/ therapeutic/ disease areas within drug development in the Immunology development unit. You will lead and integrate input from different quantitative scientists impacting clinical development, health authority interactions, represent the Advanced Quantitative Sciences function at internal and external decision boards, develop and mentor other statisticians, and provide strategic, technical, operational and scientific leadership and solutions to the organization.

Job Description

Key Responsibilities:
  • Strategic statistical input and influence into one or more projects (development plan, dose-finding strategy, regulatory strategy, publication strategy, pricing & reimbursement strategy, statistical deliverables).
  • Ensure expert level contribution to strategy (design, analysis/synthesis, interpretation and reporting, health authority response, negotiating with pricing agencies, influence and implement publication strategy, quantitative decision making) for critical studies in a program
  • Lead collaborations with clinical, regulatory and other strategic functions to drive quantitative decision making in drug development and enable successful impact on robust drug development plans
  • Collaborate across functions to ensure timeliness and quality of statistical deliverables
  • Propose and implement innovative designs and methods to optimize drug development.
  • Represent all functions within Advance Quantitative Sciences (Biostatistics, Pharmacometrics, Statistical Programming) at the Global Program Team (GPT).
  • Plan, prioritize and oversee project level activities and ensure efficient resource management within or across franchise and effective partnership with vendors.
  • Lead the review and implementation of health authority guidance.
  • Represent biostatistics in interacting with external experts (statistical, clinical, and technical).

Essential Requirements:
  • MS (in Statistics or equivalent) with 12+ years relevant work experience or PhD (in Statistics or equivalent) with 8+ years relevant work experience.
  • Has advanced knowledge of applying statistics and innovative approaches Expert knowledge in a variety of statistical areas.
  • Record of successful implementation of novel methods and/or innovative strategies in drug development
  • Extensive knowledge of drug development and HA guidelines
  • Strong understating of at least one disease area
  • Fluent English (oral and written)
  • Strong interpersonal and communication skills bridging scientific and business needs


Desirable Requirements:
  • Proven people leadership ability and expert skills in building partnerships and collaborations.


Novartis Compensation and Benefit Summary:

The pay range for this position at commencement of employment is expected to be between: $185,500 and $344,500/year; however, while salary ranges are effective from 1/1/24 through 12/31/24, fluctuations in the job market may necessitate adjustments to pay ranges during this period. Further, final pay determinations will depend on various factors, including, but not limited to geographical location, experience level, knowledge, skills, and abilities. The total compensation package for this position may also include other elements, including a sign-on bonus, restricted stock units, and discretionary awards in addition to a full range of medical, financial, and/or other benefits (including 401(k) eligibility and various paid time off benefits, such as vacation, sick time, and parental leave), dependent on the position offered. Details of participation in these benefit plans will be provided if an employee receives an offer of employment. If hired, employee will be in an at-will position and the Company reserves the right to modify base salary (as well as any other discretionary payment or compensation program) at any time, including for reasons related to individual performance, Company or individual department/team performance, and market factors.

Why Novartis:
Our purpose is to reimagine medicine to improve and extend peoples lives and our vision is to become the most valued and trusted medicines company in the world. How can we achieve this? With our people. It is our associates that drive us each day to reach our ambitions. Be a part of this mission and join us! Learn more here: https://www.novartis.com/about/strategy/people-and-culture

Youll receive:

You can find everything you need to know about our benefits and rewards in the Novartis Life Handbook.

https://www.novartis.com/careers/benefits-rewards

Accessibility and Reasonable Accommodations: The Novartis Group of Companies are committed to working with and providing reasonable accommodation to individuals with disabilities. If, because of a medical condition or disability, you need a reasonable accommodation for any part of the application process, or in order to perform the essential functions of a position, please send an e-mail to tas.nacomms@novartis.com call +1(877)395-2339 and let us know the nature of your request and your contact information. Please include the job requisition number in your message.

Join our Novartis Network: If this role is not suitable to your experience or career goals but you wish to stay connected to learn more about Novartis and our career opportunities, join the Novartis Network here: https://talentnetwork.novartis.com/network

EEO Statement:

The Novartis Group of Companies are Equal Opportunity Employers. We do not discriminate in recruitment, hiring, training, promotion or other employment practices for reasons of race, color, religion, sex, national origin, age, sexual orientation, gender identity or expression, marital or veteran status, disability, or any other legally protected status.

Accessibility and reasonable accommodations

The Novartis Group of Companies are committed to working with and providing reasonable accommodation to individuals with disabilities. If, because of a medical condition or disability, you need a reasonable accommodation for any part of the application process, or to perform the essential functions of a position, please send an e-mail to us.reasonableaccommodations@novartis.com or call +1(877)395-2339 and let us know the nature of your request and your contact information. Please include the job requisition number in your message.

Salary Range
$185,500.00 - $344,500.00

Skills Desired
Automation, Biostatistics, Clinical Trials, Computer Programming, Cross-Functional Teams, Data Analytics, Data Strategy, Decision Making Skills, Global Project Management, Metadata Management, Statistical Analysis
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