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Open nowPosted 3 hours agoWe saw it 73 min after it went up

Director, Biostatistics

Viridian Therapeutics, Inc.2 open roles

Pay
$217,000 – $250,000 a year
Where
Waltham, MA - US
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Your applicationOpen nowDirector, BiostatisticsViridian Therapeutics, Inc. · Waltham, MA - US

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The clock on this job

Early applications get read.

13.5% of postings close within 7 days. Measured by our own scanner across the market. Viridian Therapeutics, Inc. postings stay open a median of 1 days.

Share of postings closed within
  1. 2.3%1 day
  2. 4.6%3 days
  3. 13.5%7 days
  4. 21.8%14 days
  5. 36.6%30 days
  6. 58.9%60 days
This job: posted 3 hours ago

Viridian Therapeutics, Inc. median: 1 days open

The posting

At Viridian, we work with a sense of urgency for patients, creating unity with our team, the industry, and the community. We are committed to using proven science and engineering to improve the lives of people living with serious and rare diseases, and we are getting closer to achieving this goal every day.

Reporting to the Executive Director, Biometric Sciences, the Director, Biostatistics will be involved in the design, execution, analysis, and reporting clinical studies across Viridian’s development programs that are leveraging our cutting-edge Monoclonal antibody science to create transformative medicines for patients. This role is an exciting opportunity to lead and collaborate as a critical part of the clinical development group of a high performing organization.

This role may be based in our Waltham, MA headquarters, which would be a hybrid role, or it can also be fully remote. Our office-based employees are required to work in the office three (3) days a week. If remote, travel to headquarters for meetings would be required at the discretion of management.

Responsibilities (including, but not limited to):

  • Serve as the biostatistics leader & partner to our clinical development team responsible for determining clinical study strategies and manage teams to deliver results with high quality and on time
  • Champion in bringing innovative statistical thinking and methods to help drive applications of suit-for-purpose statistical methods that enhance the probability of successes for clinical development programs
  • Collaborate with internal and external Data Management stakeholders
  • Collaborate with internal and external stakeholders to ensure effective quantitative approaches are applied to the collection and analysis of a wide variety of data types
  • Provide guidance and management to contractors / consultants and manage / mentor supporting members to ensure high quality and timely deliverables.
  • Oversee development of statistical sections of clinical development plans, protocols, statistical analysis plans, and key specifications for statistical programming implementation of analyses
  • Plan, manage, and track biostatistics activities, timelines, and resources and assure operational excellence
  • Frequently interact with regulatory agencies and effectively address the statistical questions and requests
  • Review and/or author SOPs and/or Work Instructions related to biostatistics practices
  • Collaborate with and manage internal and external functions (e.g. CROs, software vendors, clinical development partners, etc.) to ensure meeting project timelines and goals
  • Manage a functional or project budget and has authority to allocate company resources according to project needs, set priorities, and ensure consistency and adherence to standards therein
  • Represent Viridian at professional societies, and in industry-wide technical discussions

Qualifications:

  • PhD (or equivalent degree) with 8+ years of relevant work experience in Biotech, Pharma, Regulatory agencies, or Clinical Research Organizations. MS (or equivalent degree) with 12+ years of relevant experience
  • Excellent statistical knowledge with the ability of applying the knowledge to solve scientific and clinical problems. Experience in Rare Diseases therapeutics clinical development is preferred
  • Proficiency in scientific computing/programming (SAS, R or Python) and implementation of advanced statistical analysis, data manipulation, graphing & simulation
  • Working knowledge of relevant FDA, EU, ICH guidelines and regulations
  • Extensive experience and excellent skillsets in managing teams and engagement of CROs, vendors, and relationship management preferred
  • Demonstrated proficiency in statistical processes including but not limited to CRF review, development of randomization lists, development of statistical analysis plan, development of CDISC submission package (SDTM, ADaM, define xml, reviewer guides), development of analysis output and review of clinical study report
  • Experience in managing external vendors
  • Prior experience supporting one or more successful BLA, NDA or MAA submissions and participating in regulatory agency meetings is strongly preferred
  • Outstanding communication skills (verbal and written)
  • Ability to manage multiple projects in a fast-paced environment
  • Ability to effectively collaborate in a dynamic, cross-functional matrix environment
  • Strong commitment to ethical standards
  • Proficient with Microsoft Office suite (i.e., Word, PowerPoint, Excel, Outlook, SharePoint, etc.)
  • Ability to travel up to 10%
  • The salary range for this position is commensurate with experience

Salary Range

$217,000—$250,000 USD

Viridian offers a comprehensive benefits package including:

  • Competitive pay and stock options for all employees
  • Medical, dental, and vision insurance
  • 100% Paid Parental Leave
  • Short- and long-term disability coverage
  • Life, Travel and AD&D
  • 401(k) Company Match with immediate company vest
  • Employee Stock Purchase plan
  • Generous vacation plan and paid company holiday shutdowns
  • Various fertility, mental, financial, and proactive physical health programs

Viridian Therapeutics, Inc. provides equal employment opportunities to all employees and applicants for employment and prohibits discrimination, harassment, or retaliation of any type without regard to race, color, religion, age, sex, national origin, disability status, genetics, protected veteran status, sexual orientation, gender identity or expression, or any other characteristic protected by Federal, State, and Local laws. Viridian will ensure that individuals with disabilities are provided reasonable accommodation to participate in the job application or interview process, to perform essential job functions, and to receive other benefits and privileges of employment. Please contact us to request accommodation.

Viridian Therapeutics, Inc participates in E-Verify, the federal program for electronic verification of employment eligibility.

Applicant Privacy Notice: Information submitted in connection with your application will be processed in accordance with Viridian's Privacy Policy, available here.

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