• AI pre-meeting research tool used by sales professionals • Helps sales professionals walk into every meeting prepared • Connects to Google Calendar and automatically delivers briefs before each call

Role Description We are seeking an Experienced Forensic Toxicologist to provide expert scientific consultation and testimony services as an independent contractor. This unique opportunity allows you to expand your professional expertise into the fascinating world of forensic science and legal consultation, where your specialized knowledge becomes crucial to the pursuit of justice. This role offers the chance to apply your toxicology expertise in high-stakes criminal and civil legal cases where you'll analyze complex scenarios involving: - Drug impairment - Poisoning cases - DUI prosecutions - Exposure incidents - Other forensic situations that require specialized scientific interpretation The ideal candidate possesses strong analytical thinking skills and can think critically when examining how substances interact with the human body under various circumstances. You'll need to consider factors such as: - Metabolism rates - Drug interactions - Timing of exposure - Individual physiological variations In this role, you will: - Review laboratory results and medical records - Provide expert scientific opinions - Testify in legal proceedings related to substance exposure, impairment, and toxicological evidence - Work with both prosecution and defense attorneys, ensuring objective scientific analysis Qualifications - Bachelor's degree in chemistry or related scientific field required - At least 2 years of related laboratory experience in testing blood and other bodily fluids - Experience with microscopic techniques, chromatography, and spectrograph analysis - Forensic/Criminology laboratory background preferred - Excellent written and verbal communication skills - Ability to explain complex toxicology concepts in layman's terms - Strong analytical and critical thinking abilities - Professional demeanor and appearance for testimony - Attention to detail and accuracy in documentation - Ability to work independently and meet deadlines - Proficiency with electronic records and computer systems Requirements - Dedicated, quiet, and distraction-free working space - Access to high-speed internet connection - Ability to maintain professional appearance and environment during video conferences - Availability to accept cases on short notice when needed - Maintain current professional liability insurance - Comply with all confidentiality and non-disclosure requirements - Maintain professional standards and ethical conduct - Clean criminal background - Must be able to sit at a computer for extended periods and stand/walk during court appearances - Ability to effectively communicate with clients, attorneys, and colleagues via phone, video conference, and in-person meetings - Must be able to see details on computer screens, read printed materials, and review pdf documents Benefits - Marketing Support: We promote your expertise to potential clients and help showcase your qualifications to expand your professional network. - Administrative Support: Our team handles all billing, funding, and paperwork coordination. - Streamlined Payment Processing: We offer secure direct deposit payments through Melio for convenient and timely compensation. - Professional Development: Opportunities for continued learning and growth in forensic toxicology through exposure to diverse and challenging cases. - Expert Network: Access to collaborate with a network of medical and forensic professionals across multiple specialties. - Cancellation Bonus: Cancellation bonus available if testimony is cancelled within 10 days of scheduled date. - Case Variety: Exposure to diverse and interesting cases across multiple legal areas including DUI, homicide, assault, and civil litigation.

Role Description The Principal, Pharmacovigilance / Device Vigilance is a detail-oriented and proactive professional supporting the safety surveillance of In Vitro Diagnostic and Software-driven products across their lifecycle, including clinical studies and post-market activities. This role is responsible for the collection, assessment, reporting, and management of adverse events, product complaints, and safety data for both medicinal products and medical devices, ensuring compliance with global regulatory requirements. The position plays a critical role in ensuring compliance with global regulatory requirements (e.g., FDA, EU IVDR, Japan) and maintaining the highest standards of patient safety and product quality across both laboratory-developed tests and regulated IVD products, including software/algorithm-based components. Qualifications - Bachelor’s degree in life science field (biology, microbiology, chemistry, engineering, medical technology, regulatory science, etc.) or equivalent. Advanced degree in life sciences (MS, PhD, etc.) and/or MBA preferred. - RAC preferred. - Minimum of 12 years of direct applicable experience in pharmacovigilance and/or device vigilance. - Strong knowledge of global safety regulations (FDA, EMA, ICH, EU IVDR, Japan). - Experience with safety databases (e.g., AEMS, Argus, ARISg, Veeva Safety). - Familiarity with MedDRA coding and case processing workflows. - Knowledge of applicable standards, including ISO 13485 and ISO 14971. Requirements - Experience with global markets is highly desirable. - Strong analytical and clinical assessment skills. - Attention to detail and regulatory compliance mindset. - Ability to manage multiple priorities and deadlines. - Excellent written and verbal communication. - Cross-functional collaboration. - Demonstrated self-starter and highly motivated, energetic and enthusiastic. - Ability to exercise independent judgment and discretion within a broadly defined range of policies and practices, which includes analytical problem solving. - Demonstrated organizational, planning, and program management skills, including action oriented, focused urgency and driving for results. - Ability to be effective in complex projects with ambiguity and/or rapid change. - Excellent written and verbal communication skills including ability to communicate across cultures. - Work with others in a team environment; effective interactions with technical and medical personnel. - Computer literacy (PC, Microsoft Office and Google Workspace). Benefits - Competitive Benefits - Employee benefits include comprehensive medical, dental, vision, life and disability plans for eligible employees and their dependents. - Natera employees and their immediate families receive free testing in addition to fertility care benefits. - Other benefits include pregnancy and baby bonding leave, 401k benefits, commuter benefits and much more. - Generous employee referral program. Company Description Natera™ is a global leader in cell-free DNA (cfDNA) testing, dedicated to oncology, women’s health, and organ health. Our aim is to make personalized genetic testing and diagnostics part of the standard of care to protect health and enable earlier and more targeted interventions that lead to longer, healthier lives. The Natera team consists of highly dedicated statisticians, geneticists, doctors, laboratory scientists, business professionals, software engineers and many other professionals from world-class institutions, who care deeply for our work and each other. When you join Natera, you’ll work hard and grow quickly. Working alongside the elite of the industry, you’ll be stretched and challenged, and take pride in being part of a company that is changing the landscape of genetic disease management.

Role Description The Pharmacovigilance Physician is a medical physician (MD, DO, or equivalent) responsible for: - Medical review of individual case safety reports (ICSR) to determine benefit-risk analysis. - Providing medical assessment statements. - Reviewing and analyzing aggregate data sets for benefit-risk assessments. - Reviewing and interpreting clinical and post-marketing data for signal detection, evaluation, and verification. - Participating in safety meetings with clients. - Assisting in drafting, reviewing, and refining medical-content intensive portions of periodic safety reports (PADERs, PSURs, DSURs, PBRERs, IND Annual Reports). - Updating Investigators Brochure (IB) and Clinical Safety Summaries (ISS). - Handling US and international product labeling documents and ad hoc safety information requests from regulatory authorities. - Drafting, reviewing, and refining risk management plans and risk evaluation and mitigation strategies. - Supporting the Qualified Person for Pharmacovigilance as required. Qualifications - Licensed medical physician in good-standing in the state(s) of licensure (MD, DO, etc.) plus one (1) year pharmacovigilance experience or other equivalent experience. - Or unlicensed medical physician (MD, DO, etc.) with no record of past or present Medical Board disciplinary action; plus ten (10) years of combined pharmacovigilance experience, clinical healthcare provider experience, or other equivalent experience. Requirements - Self-Motivated - Ability to be internally inspired to perform a task to the best of one's ability using his or her own drive or initiative. - Organized - Possessing the trait of being organized or following a systematic method of performing a task. - Prefer board certification in related area for client being supported. - Epidemiology degree is a plus. - One year related pharmacovigilance experience in the pharmaceutical industry or other equivalent experience, such as clinical trial investigator, health authority inspector, epidemiologist, etc. - Prefer proficiency with Microsoft Office and content management systems. - Understanding of legal, regulatory and compliance requirements with regards to pharmacovigilance based on global regulations for EU, FDA, Japan MHLW, UK MHRA, and other entities, and ICH guidelines. Company Description