Welcome page Returning Candidate? Log back in! Principal Bioinformatician Computational Lead Location : Location US-NC-Raleigh ID 2024-4975 Category Operations Type Full Time - Permanent Overview

Principal Bioinformatician Computational Lead

Responsibilities

The Principal Bioinformatician Computational Lead oversees the development and implementation of a multi-site effort in computational toxicology and pharmacology services, primarily located at the Raleigh/Research Triangle Park (RTP) office of Inotiv. They are part of a multidisciplinary team supporting the development, validation, and evaluation of alternative toxicological methods for implementation in international regulatory testing.

 

They are expected to have a working knowledge of biology, biochemistry, toxicology, pharmacology and/or statistics. Experience with error corrected next-generation sequencing and analysis of data from this technology is an asset. The Principal Bioinformatician uses or develops computational methods to analyze, simulate, visualize, and predict the toxicological or pharmacological effects of chemicals from in vivo and in vitro studies.

 

They will consult on experimental design and statistical analysis and coordinate project timelines associated with the implementation of these analyses. They are expected to assist as necessary in all aspects of data analysis, including data curation, statistical evaluation, data management, and preparation for/conducting analyses using predefined computational workflows. Dissemination of information needed by U.S. governmental committees and regulatory agencies, stakeholder working groups, peer review panels, and test method developers is an essential part of this position. Likewise, preparation of scientific and technical documents such as presentations, reports, workshop summaries, manuscripts, and operating procedures are core components of this position.

 

The Principal Bioinformatician is responsible for growing the computational toxicology team, including training, mentoring, and recruiting. They are expected to actively participate in business development and work in a team environment where cooperation and a professional attitude are essential. Other duties will be assigned as needed.

Qualifications

Required:

M.S./Ph.D. in related scientific field with at least 8/5 years post-degree experience in bioinformatics, computational biology/toxicology, (bio)statistics and/or data analysis.Demonstrated proficiency in data manipulation using the programming languages R, SAS, or python.Experience writing and editing technical documentsExcellent verbal and written communication skills.Strong history of working across multiple sites, with customers, and other stakeholders.Experience working well independently and in a team environment

Preferred

Familiarity with working in a Good Laboratory Practices (GLP) environment.Experience analyzing RNAseq and DNAseq data.Experience in cheminformatics or computational toxicology.Familiarity with KNIME.Familiarity with supervised and unsupervised learning techniques.

Please include a description of any relevant experience in the areas of demonstrated proficiency described in the qualifications.

 

A successful team member will be a service-oriented team player who is able to work on a variety of concurrent projects within the area of pharmacology and toxicology. They will work cooperatively with diverse teams and communicate their science effectively to non-technical clients. This position is based in RTP, NC and is eligible for remote work in the U.S.

 

 

*This position could be offered at different levels for candidates who qualify with a combination of advanced levels of education and/or years of experience.  The salary range will adjust along with the level of the role to match the person’s relevant experience and/or education level.

 

Inotiv is a growing contemporary drug discovery and development company where we “Play to Win” in an industry rich with opportunity.  Together, we face challenges and together we win in the delivery of world-class drug discovery and development solutions that impact the health and well-being of people all over the world.  There’s an opportunity for everyone at all phases of a career, each individual’s unique skill set has an impact on the work we conduct. If you have the talent and desire to impact the quality of people’s lives, we have the career opportunities to make it happen.  Join us in embracing research and science to impact the health and well-being of people all over the world.

 

Inotiv has been named a 2023 Top Workplace!

Salary will be commensurate with experience and responsibilities. Benefits include health and dental coverage, short- and long-term disability, paid time off, paid parental leave, 401K, and more!

 

Inotiv is an Equal Opportunity Employer. It is our policy to provide a fair and equal employment opportunity to all persons, regardless of age, race, color, religion, sex, gender, gender identity, gender expression, sexual orientation, genetic information, disability, national origin, veteran status, or any other basis prohibited by law. This policy governs all aspects of employment, including selection, job assignment, compensation, discipline, termination and access to benefits and training.

 

#LI-JM1

Options Apply for this job onlineApplyShareEmail this job to a friendRefer Sorry the Share function is not working properly at this moment. Please refresh the page and try again later. Share on your newsfeed Application FAQs

Software Powered by iCIMS
www.icims.com