Inotiv · 1 day ago
Senior Scientific Director
Inotiv is a growing contemporary drug discovery and development company, and they are seeking a Senior Scientific Director for Genetic Toxicology to shape the scientific strategy for preclinical and regulatory services. The role involves leading the Genetic Toxicology program, ensuring scientific excellence, and maintaining regulatory compliance while serving as a primary advisor for clients in various sectors.
BiopharmaLife ScienceMedical DevicePharmaceutical
Responsibilities
Serve as the primary scientific advisor for clients in the pharmaceutical, chemical, and consumer product sectors, providing insights on genetic toxicology study design and compliance with international regulations
Identify and establish partnerships with pharmaceutical, chemical, and consumer product companies to expand service offerings and enhance market presence
Partner with Business Development to support client relationships and create compelling technical proposals that highlight the scientific and regulatory strengths of our genetic toxicology capabilities
Represent Inotiv at global scientific and regulatory meetings, conferences, and working groups focusing on Genetic Toxicology
Drive internal R&D initiatives to expand Inotiv’s genetic toxicology service portfolio by leading innovative technologies validations
Collaborate with Quality Assurance Unit to maintain the highest GLP and OECD compliance standards
Mentor and develop scientific staff, cultivating a high-performance culture focused on scientific excellence
Other special projects and duties as assigned
Qualification
Required
Ph.D. in Toxicology, Genetic Toxicology, or related field
Minimum 10+ years of progressive experience in genetic toxicology, preferably within a CRO and/or regulated industry
At least 5 years in senior scientific leadership managing GLP-compliant genetic toxicology programs
Track record of successful client collaboration and program delivery
Peer-reviewed publications or industry recognition in genetic toxicology
Strong understanding of global regulatory frameworks governing genetic toxicology and study design; familiarity with business development processes in the CRO testing industry
Strategic scientific vision combined with business acumen
Excellent communication, analytical, and problem-solving skills, with the ability to effectively convey complex scientific information to diverse stakeholders
Strong leadership, mentorship, and communication skills
Demonstrated ability to build trusted client relationships
Experience driving innovation and process improvement in a dynamic, fast-paced environment
Extended computer and display screen equipment usage
Ability to push, pull, lift 5 pounds unassisted
Stand / walk for extended period of time
Fine manipulation including handle touch object or tools and ability to handled controls to perform work
Ability to read and interpret materials, verbally communicate, and hear required
Benefits
Health and dental coverage
Short- and long-term disability
Paid time off
Paid parental leave
401K
And more
Company
Inotiv
Inotiv provides biopharmaceutical analytical, reproductive toxicology, medical device testing, DMPK, consulting and pathological services.
H1B Sponsorship
Inotiv has a track record of offering H1B sponsorships. Please note that this does not
guarantee sponsorship for this specific role. Below presents additional info for your
reference. (Data Powered by US Department of Labor)
Distribution of Different Job Fields Receiving Sponsorship
Represents job field similar to this job
Trends of Total Sponsorships
2025 (1)
2024 (1)
2023 (2)
2022 (1)
Funding
Current Stage
Public CompanyTotal Funding
$27.64MKey Investors
Indiana Economic Development Corporation
2024-12-18Post Ipo Equity· $27.6M
2022-06-20Grant· $0.04M
1997-11-28IPO
Recent News
2025-12-13
2025-12-11
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