Viridian Therapeutics

Director, Biostatistics , Biometric Sciences

Viridian Therapeutics$150K — $180K *
Pharmaceuticals & Biotech
8 - 10 years of experience
Job Overview by Ladders

Qualifications

  • PhD or equivalent with 8+ years in biotech, pharma, or clinical research, or MS with 12+ years.
  • Strong statistical knowledge applied to scientific problems, preferably in rare diseases.
  • Proficiency in scientific programming (SAS, R, Python) for statistical analysis.
  • Familiarity with FDA, EU, and ICH guidelines and regulations.
  • Extensive experience managing teams and CRO/vendor relationships.
  • Proficient in statistical processes related to clinical study reports and submissions.
  • Outstanding verbal and written communication skills.

Responsibilities

  • Lead biostatistics efforts in collaboration with clinical development teams.
  • Innovate statistical methods to enhance clinical program success rates.
  • Facilitate collaboration with data management and external stakeholders.
  • Guide contractors and mentor team members for timely and high-quality deliverables.
  • Oversee the development of statistical sections for clinical documents.
  • Plan and manage biostatistics activities, resources, and timelines.
  • Engage with regulatory agencies regarding statistical inquiries.

Benefits

  • Competitive pay and employee stock options.
  • Comprehensive medical, dental, and vision insurance.
  • 100% Paid Parental Leave.
  • Short- and long-term disability coverage.
  • 401(k) Company Match with immediate vesting.
  • Generous vacation plan and paid holiday shutdowns.
  • Access to various health programs including mental and financial wellness.
Full Job Description
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): 3 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 3 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 3 Collaborate with internal and external Data Management stakeholders 3 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 3 Provide guidance and management to contractors / consultants and manage / mentor supporting members to ensure high quality and timely deliverables. 3 Oversee development of statistical sections of clinical development plans, protocols, statistical analysis plans, and key specifications for statistical programming implementation of analyses 3 Plan, manage, and track biostatistics activities, timelines, and resources and assure operational excellence 3 Frequently interact with regulatory agencies and effectively address the statistical questions and requests 3 Review and/or author SOPs and/or Work Instructions related to biostatistics practices 3 Collaborate with and manage internal and external functions (e.g. CROs, software vendors, clinical development partners, etc.) to ensure meeting project timelines and goals 3 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 thereiRepresent Viridian at professional societies, and in industry-wide technical discussions Requirements Qualifications: 3 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 3 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 3 Proficiency in scientific computing/programming (SAS, R or Python) and implementation of advanced statistical analysis, data manipulation, graphing & simulation 3 Working knowledge of relevant FDA, EU, ICH guidelines and regulations 3 Extensive experience and excellent skillsets in managing teams and engagement of CROs, vendors, and relationship management preferred 3 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 3 Experience in managing external vendors 3 Prior experience supporting one or more successful BLA, NDA or MAA submissions and participating in regulatory agency meetings is strongly preferred 3 Outstanding communication skills (verbal and written) 3 Ability to manage multiple projects in a fast-paced environment 3 Ability to effectively collaborate in a dynamic, cross-functional matrix environment 3 Strong commitment to ethical standards 3 Proficient with Microsoft Office suite (i.e., Word, PowerPoint, Excel, Outlook, SharePoint, etc.) 3 Ability to travel up to 10% 3 The salary range for this position is commensurate with experience Viridian offers a comprehensive benefits package including: 3 Competitive pay and stock options for all employees 3 Competitive medical, dental, and vision insurance 3 100% Paid Parental Leave 3 Short- and long-term disability coverage 3 Life, Travel and AD&D 3 401(k) Company Match with immediate company vest 3 Employee Stock Purchase plan 3 Generous vacation plan and paid company holiday shutdowns 3 Various fertility, mental, financial, and proactive physical health programs

About Viridian Therapeutics

Viridian Therapeutics is a biotechnology company that develops gene therapies for inherited diseases. The company's lead product candidate, VRDN-001, is a gene therapy for Friedreich's ataxia, a rare genetic disease that causes progressive damage to the nervous system. Viridian Therapeutics was founded in 2018 and is headquartered in Cambridge, Massachusetts.
Learn more about Viridian Therapeutics
Size
10 employees
Market Cap
$1.1 billion
Industry
Net Income
-$30 million
5 Year Trend
-3.1%
Revenue
$1.8 million
NASDAQ

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