Management Analyst SME

Position Details: 

Job Title: Management Analyst SME 

Job Type: Full-time 

Location: Remote, MD 

Revised: 9/12/2025 

Dynanet Corporation Overview: 

Dynanet started with a focus on IT infrastructure and operations, helping organizations enhance their networks and overcome the limitations of 1990s technology. From strengthening communication channels to introducing innovative ways to collaborate and share information, Dynanet played a crucial role in shaping the early stages of digital transformation. The company’s efforts helped organizations build the very fabric of connectivity that now powers our modern world. Over the last three decades, Dynanet has grown into a trusted partner for organizations looking to innovate boldly and transform seamlessly. While technology continues to evolve and unlock new opportunities, for nearly 30 years, Dynanet remains committed to delivering cutting-edge solutions that drive lasting change for its customers. Through agility, foresight, and an unwavering dedication to excellence, Dynanet continues to empower organizations to thrive in a rapidly changing digital landscape. Our story is more than just a story of technology – it’s a story of vision, growth, and transformation that has shaped the past and continues to pave the way for the future. 

About the Role: 

The Management Analyst (SME – Regulatory Toxicology) provides scientific and technical expertise in regulatory toxicology to support the Collection of Alternative Methods for Regulatory Application (CAMERA) project, a web-based resource for validated and qualified New Approach Methodologies (NAMs). The incumbent serves as the principal interface between toxicology subject matter experts and the information technology team to ensure accurate integration of regulatory science data into CAMERA. 

Roles & Responsibilities: 

• Guides the implementation of curated toxicology data from validated and regulatory-accepted test guidelines into the CAMERA system. 
• Serves as liaison between scientific stakeholders and IT developers to translate regulatory science requirements into technical specifications. 
• Reviews and validates toxicological data for accuracy, consistency, and regulatory compliance prior to system integration. 
• Contributes to the development of standardized vocabularies, metadata structures, and ontologies to support regulatory application of NAMs. 
• Provides expertise in the scientific review of New Approach Methodologies (NAMs), including applicability and relevance to U.S. and international regulatory frameworks. 
• Prepares technical reports, analyses, and briefing materials to inform decision-makers, program managers, and external stakeholders. 
• Recommends process improvements to enhance data quality, interoperability, and system usability in support of regulatory submissions. 

Required Professional Skills: 

• Demonstrated knowledge of U.S. and international regulatory testing guidelines (e.g., OECD, EPA, FDA). 
• Familiarity with alternative test methods, NAMs, and their validation/qualification processes. 
• Ability to analyze, interpret, and apply scientific data in regulatory contexts. 
• Strong communication skills to effectively convey technical content to scientific and non-scientific audiences. 

Preferred Professional Skills: 

• Methodologies (NAMs), including validation and qualification processes. 
• Experience with scientific databases, controlled vocabularies, and regulatory data standards (e.g., IUCLID, SEND, OECD harmonization). 
• Prior experience supporting federal contracts or working with regulatory agencies. 

Dynanet Team Requirements and Expectations: 

• Possess Strong written and verbal communication skills. 
• Highly organized with an ability to prioritize, balance, and effectively advance multiple competing priorities in a high-volume, fast-paced environment. 
• Ability to interact in a professional and collaborative manner with fellow Dynanet Teammates and the clients, and business partners that we work with. 
• Ability and desire to challenge and educate yourself to support and advance IT services delivery in the Federal agencies we serve. 
• Excellent judgment and creative problem-solving skills. 
• Respond to team member and client requests via email, MS teams, or other communication means during core business hours. 
• Active listening skills to understand clients' needs, and collaboration skills to work with other developers and designers. 

Education/Experience Requirements: 

• Master’s degree or higher in toxicology, pharmacology, regulatory science, or related biological/health sciences. 
• Minimum of 2 years of research or professional experience in regulatory toxicology. 

Employee Benefits Overview: 

• Industry Competitive Compensation 
• Medical and Dental Insurance 
• Paid Time Off/Holidays 
• 401(k) Retirement Plans with Matching 
• Remote Work 
• Paid Training 
• Employee Referral Program 
• Employee Development Program