Role Description We are looking for a Senior Epidemiologist to manage and analyze critical health data related to environmental diseases and conditions for the Florida Environmental Public Health Tracking program. In this role, you will play a vital part in monitoring public health significance through various data sources, including: - ESSENCE-FL - Hospital Discharge Data - Emergency Department Data - Vital Statistics - The Florida Birth Defects Registry - The Florida Cancer Registry Preferred candidates would be located in Tallahassee, Florida. WiredPeople is open to remote candidates residing within Florida state lines. Qualifications - Working knowledge and deep understanding of public health scientific principles and policies related to epidemiology. - Proven capacity to effectively prioritize workloads and consistently meet project deadlines. - Exceptional written and oral communication skills, with the interpersonal finesse required to collaborate seamlessly with various staff members, program partners, and external agencies. - Strong organizational skills with the ability to manage multiple complex priorities and projects simultaneously. Requirements - Data Analysis & Surveillance - Review existing API feeds and data sources concerning air, water, and soil quality conditions of public health significance. - Analyze trends over time for environmental health conditions. - Monitor data submitted to the Florida Tracking site and data explorer portal. - Work alongside the integration broker to ensure submitted files are accurately received and displayed. - Troubleshoot system connectivity, evaluate data anomalies, and propose solutions to system bugs. - Reporting & Technical Assistance - Produce and disseminate annual summary reports using data from the Agency for Health Care Administration and Vital Statistics. - Provide technical assistance, consultative services, and direction for the development, implementation, and evaluation of environmental health data sources. - Support the compilation of performance metrics for the Environmental Public Health Tracking Cooperative Agreement. - Assist county health departments in designing and evaluating health initiatives aimed at improving environmental health indicators. - Summarize weekly activities and present key findings. - Collaboration & Policy Development - Create and update Standard Operating Procedures (SOPs) related to environmental health conditions. - Serve as a primary liaison in 3 different areas. - Ensure strict compliance with all Department data security and confidentiality procedures. Company Description WiredPeople provides equal employment opportunities (EEO) to all employees and applicants for employment without regard to race, color, religion, sex, national origin, age, disability or genetics. In addition to federal law requirements, WiredPeople complies with applicable state and local laws governing nondiscrimination in employment in every location in which the company has facilities. This policy applies to all terms and conditions of employment, including recruiting, hiring, placement, promotion, termination, layoff, recall, transfer, leaves of absence, compensation and training.

Role Description Centific AI Research seeks a PhD Research Intern to design and evaluate speech‑first models, with a focus on Spoken Language Models (SLMs) that reason over audio and interact conversationally. You’ll move ideas from prototype to practical demos, working with scientists and engineers to deliver measurable impact. Scope of Work - End‑to‑end speech dialogue systems (speech‑in/speech‑out) and speech‑aware LLMs. - Alignment between speech encoders and text backbones via lightweight adapters. - Efficient speech tokenization and temporal compression suitable for long‑form audio. - Reliable evaluation across recognition, understanding, and generation tasks—including robustness and safety. - Latency‑aware inference for streaming and real‑time user experiences. Example Projects - Prototype a conversational SLM using an SSL speech encoder and a compact adapter on an existing LLM; compare against strong baselines. - Create a data recipe that blends conversational speech with instruction‑following corpora; run targeted ablations and report findings. - Build an evaluation harness that covers ASR/ST/SLU and speech QA, including streaming metrics (latency, stability, endpointing). - Ship a minimal demo with streaming inference and logging; document setup, metrics, and reliability checks. - Author a crisp internal write‑up: goals, design choices, results, and next steps for productionization. Qualifications - PhD candidate in CS/EE (or related) with research in speech, audio ML, or multimodal LMs. - Fluency in Python and PyTorch, with hands‑on GPU training; familiarity with torchaudio or librosa. - Working knowledge of modern sequence models (Transformers or SSMs) and training best practices. - Depth in at least one area: - (a) discrete speech tokens/temporal compression, - (b) modality alignment to LLMs via adapters, or - (c) post‑training/instruction tuning for speech tasks. - Strong experimentation habits: clean code, ablations, reproducibility, and clear reporting. Preferred Qualifications - Experience with speech generation (neural codecs/vocoders) or hybrid text+speech decoding. - Background in multilingual or code‑switching speech and domain adaptation. - Hands‑on work evaluating safety, bias, hallucination, or spoofing risks in speech systems. - Distributed training/serving (FSDP/DeepSpeed), and experience with ESPnet, SpeechBrain, or NVIDIA NeMo. Tech Stack - PyTorch, CUDA, torchaudio/librosa; experiment tracking (e.g., Weights & Biases). - LLM backbones with lightweight adapters; neural audio codecs and vocoders as needed. - FastAPI/gRPC for services; ONNX/TensorRT and quantization for efficient inference. Logistics - Location: Redmond (Preferred) or Remote - Duration: <3–6 months> Benefits - Competitive stipend and hands-on projects with measurable real-world impact. - Mentorship from applied scientists and engineers; opportunities to publish and present. - Access to modern GPU infrastructure and a supportive environment for fast, responsible experimentation. - Flexible location and schedule options, subject to team needs. - Rate: $40 per Hour Company Description Centific is a frontier AI data foundry that curates diverse, high-quality data, using our purpose-built technology platforms to empower the Magnificent Seven and our enterprise clients with safe, scalable AI deployment. Our mission is to bridge the gap between AI creators and industry leaders by bringing best practices in GenAI to unicorn innovators and enterprise customers.

Role Description ICF seeks an Environmental Scientist to provide technical and training support for our U.S. Environmental Protection Agency (EPA) projects with the Office of Superfund and Emergency Management (OSEM), Office of Brownfields and Land Revitalization (OBLR), and Office of Resource Conservation and Recovery (ORCR). This is an on-call, part-time hours position based on project needs. - Support identifying and evaluating ways to advance contaminated site cleanup including development of site strategies, RI/FS scoping, conceptual site models, optimization recommendations, cost estimates and advising on use of innovative technologies and best practices. - Leverage hands-on knowledge and experience with site characterization and remediation to promote improvements to the cleanup of contaminated sites. - Provide support to development and facilitation of training materials. - Manage multi-disciplinary project teams and client engagement. Qualifications - Master’s degree in biology, environmental science, or related technical field. - Minimum 2 years of experience supporting EPA’s Superfund Removal and Remedial Programs. - Knowledge of EPA cleanup programs and policies, particularly CERCLA and RCRA. - Expertise in leading and developing technical deliverables and training materials. Requirements - Team player with demonstrated project management skills including the ability to work in a fast-paced environment. - Demonstrated ability to effectively engage with clients. - Excellent written and oral communications skills. Benefits - ICF is a global advisory and technology services provider. - We combine unmatched expertise with cutting-edge technology to help clients solve their most complex challenges. - We are an equal opportunity employer. - Reasonable Accommodations are available for disabled veterans, individuals with disabilities, and individuals with sincerely held religious beliefs. - Pay range for this position based on full-time employment is: $55,665.00 - $94,631.00.

Role Description Premier Research is looking for a Pharmacovigilance Physician II to join our Pharmacovigilance and Records Management team. You will help biotech, medtech, and specialty pharma companies transform life-changing ideas and breakthrough science into new medicines, devices, and diagnostics. What we do is profoundly connected to saving and improving lives, and we recognize our team members are the most valuable asset in delivering success. We are here to help you grow, to give you the skills and opportunities to excel at work with the flexibility and balance your life requires. Your ideas influence the way we work, and your voice matters here. As an essential part of our team, you help us deliver the medical innovation that patients are desperate for. Join us and build your future here. What You'll Be Doing: - Conducts medical assessment of all safety related data (AEs, SAE, SUSAR, AESI etc.) as per the project contract. - Ensures medical accuracy of case narratives, coding and medical sense of all cases and ensures appropriate queries are raised to expedite case closure. - Provides analysis of similar events (AOSE). - Writes safety section, including benefit risk assessment of all aggregate safety reports such as Periodic Drug Safety Reports (PSURs), Periodic Adverse Drug Experience Reports (PADERs), DSUR/IND Annual reports and line listings of Suspected Unexpected Serious Adverse Reactions (SUSARs) for regulatory submission. - Reviews Safety Management Plans. - Ensures compliance with and adherence to all internationally recognized standards (e.g. ICH GCP, ICH E2A, ISO14155, etc.), national regulations and SOPs applicable for specific projects. - Ensure ongoing safety monitoring of investigational and marketed products to include detection of signal and assessment of risk, assessment of the risk-benefit balance of products and analysis of the overall safety of products. - Medical contribution to risk management activities including Risk Management Plans (RMP) and Risk Evaluation and Minimization Strategy (REMS). - Attends Investigator Meetings and interacts with Investigative site staff and client representatives as needed. - Reviews study documentation (e.g. budget, protocol, CRF, IB, etc.). - Supports the Head of PV in aligning medical safety processes and procedures with the overall company PV strategy. Qualifications - Graduate in medicine. - Extensive clinical practice experience in oncology, dermatology, pediatrics, or neuro-psychiatry is preferred (Board certification or equivalent not required). - Excellent understanding of global PV regulatory environment with working knowledge of international regulations, initiatives, standards including FDA CFRs, EU Regulations and aligned guidance documents, EU GVP modules and ICH/ EU and FDA GCP Clinical Safety specific guidance. - CRO experience is preferred. - 2 or more years’ experience of working in a medical or safety department evaluating patient safety data. - Demonstrable knowledge of medical terminology and experience of handling medical data review and query resolution. - Familiar with MedDRA, WHODRL and safety databases such as ARGUS and electronic data capture systems is preferred. - Be able to diagnose problems quickly and have foresight into potential issues with an aptitude in decision-making and problem-solving. - Attention to accuracy, consistency and detail oriented. - Ability to read, write and speak fluent English. - Excellent organizational and time-management skills, able to prioritize work to meet deadlines.