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Associate Director, Biostatistics

Harmony Biosciences LLC
Posted 18 hours ago, valid for 17 days
Location

Plymouth Meeting, PA, US

Salary

Competitive

Contract type

Full Time

Paid Time Off
Life Insurance
Disability Insurance
Wellness Program

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Sonic Summary

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  • Harmony Biosciences is seeking an Associate Director, Biostatistics for their Plymouth Meeting location, requiring a Master's Degree in Biostatistics and a PhD is preferred.
  • Candidates must have over 5 years of experience in applying statistical methods in biomedical research, along with 3+ years in pharmaceutical and/or CRO settings.
  • The role involves managing complex projects, supporting regulatory interactions, and ensuring statistical soundness of project deliverables.
  • The position offers a competitive salary and a benefits package that includes medical, dental, and vision coverage, as well as paid time off and a 401(k) plan.
  • Candidates should possess advanced knowledge in statistical methods relevant to clinical development and strong programming skills in SAS, with R proficiency being a plus.

Harmony Biosciences is recruiting for an Associate Director, Biostatistics inĀ our Plymouth Meeting location. In this role you will work within the Clinical Biostatistics team to ensure accurate information processing for data integrity, quality, and efficiency. Manages complex projects, supports interactions with regulatory authorities and key opinion leaders, and is accountable for the statistical soundness of all statistical input and deliverables for assigned projects. Partners with the Clinical team on clinical trial design and available statistical methodologies and their application in drug development. Participates in the development and application of standards and process improvement within the Clinical Biostatistics team.



Responsibilities include but are not limited to:

  • Actively supports clinical development teams on statistical elements of study design, analysis and decision-making issues. Advises on available statistical methodologies, performs modeling and simulations, and leverages external experts, as needed
  • Contributes to the development and evaluation of technical infrastructure to facilitate efficient execution and evaluation of clinical trials
  • Contributes to the selection, implementation and execution of statistical methodologies and related processes
  • Reviews key project and study documents to ensure optimal statistical presentation and complianceĀ 
  • Facilitates and oversees creation of standards with respect to key variables, definitions, statistical methods, data structures and presentation of dataĀ 
  • Contributes to the preparation of statistical aspects for meetings with regulatory authorities, key opinion leaders and similar experts and bodies
  • Interacts with and supports the Clinical teams’ interactions with clinical investigators, as needed, to determine protocol design
  • Evaluates databases and statistical analysis programs to determine optimal technical solutionsĀ 
  • Maintains awareness of new methodology in statistics and updates in regulatory guidelines, and signals relevant developments in a timely manner for the project teams



Qualifications:

  • Master’s Degree in Biostatistics required, PhD preferred
  • 5+ years of experience in applying statistical methods in biomedical researchĀ 
  • 3+ years of pharmaceutical and/or CRO experience required
  • 3+ years of ADaM experience required
  • Experience with all stages of clinical development, especially late stage experience strongly preferred
  • Advanced and broad knowledge of statistical methods, along with thorough understanding of industry practices related to the statistical analysis of clinical data
  • Advanced knowledge in a variety of statistical methods with applications in clinical development
  • Experience in statistical and data requirements for health authorities such as FDA; experience in statistical and data requirements for European regulatory bodies and PMDA is a plus
  • Experience in all aspects of statistics for clinical trials and in working as a member of a project team including design of clinical studies
  • Strong understanding of the various functions and expert groups contributing to Drug Development
  • Strong programming skills in SAS; proficiency with R programming is a plusĀ 

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Physical demands and work environment:

  • Domestic travel is estimated to be up to 5% of the time for this position.
  • While performing the duties of this job, the noise level in the work environment is usually quiet.
  • While performing the duties of this job, the noise level in the work environment can vary from relatively quiet (remote or office) to moderate.
  • The employee must be able to occasionally lift and/or move more than 20 pounds.
  • Specific vision abilities required by this job include: Close vision.
  • Manual dexterity required to use computers, tablets, and cell phone.
  • Continuous sitting for prolonged periods.



What can Harmony offer you?

  • Medical, Vision and Dental benefits the first of the month following start date
  • Generous paid time off and Company designated HolidaysĀ 
  • Company paid Disability benefits and Life Insurance coverageĀ 
  • 401(k) Retirement Savings Plan
  • Paid Parental leaveĀ 
  • Employee Stock Purchase Plan (ESPP)Ā 
  • Company sponsored wellness programsĀ 
  • Professional development initiatives and continuous learning opportunities
  • A certified Great Place to WorkĀ® for eight consecutive years based on our positive, values-based company cultureĀ 

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Harmony Biosciences is a pharmaceutical company headquartered in Plymouth Meeting, PA. The company was established in October 2017 with a vision to provide novel treatment options for people living with rare, neurological disorders who have unmet medical needs. For more information on Harmony Biosciences, visitĀ www.harmonybiosciences.com


Harmony Biosciences is an Equal Opportunity, e-Verify Employer. All qualified applicants will receive equal consideration for employment without regard to race, color, national origin, religion, sex, pregnancy, marital status, sexual orientation, gender identity/expression, age, disability, genetic information, military service, covered/protected veteran status or any other federal, state or local protected class.

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Recruitment agencies please note: Harmony Biosciences will only accept applications from agencies/business partners that have been invited to work on a specific role. Candidate Resumes/CV's submitted without permission or directly to Hiring Managers will be considered unsolicited and no fee will be payable. Thank you for your cooperation.Ā 



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