Support partner organizations in Mexico by developing the scientific and factual basis for legal and administrative advocacy to protect the climate and the environment.
Compensation
The salary range for this position is MXN 720,000 – 900,000 (approximately USD 42,000 – 52,500).
Responsibilities
Evaluate the scientific and technical basis for potential cases, issues, or advocacy opportunities
Review and summarize existing scientific, technical, and quantitative studies across a broad range of fields including those related to fossil fuel and energy infrastructure, air quality, toxics, biodiversity, and public health
Review environmental impact assessments, data, technical reports, and other environmental planning documents for rigor, accuracy, methodological soundness, and consistency with accepted scientific approaches
Synthesize scientific and technical information and make it accessible for non-technical audiences to support legal strategy, advocacy, communications, and decision-making
Draft scientific and technical content in accessible language suitable for legal filings, reports, fact sheets, presentations, client materials, media materials, and other internal or external products
Requirements
Master’s degree or Ph.D. in a natural science, environmental engineering, public health, or a related field of environmental science, or the equivalent level of research and analytic experience
Research Technician II- Silverman Lab
Children's Hospital of Philadelphia · Posted Oct 14, 2026
Senior analytical and strategic partner to the CFO / Head of Corporate Strategy, Business Development, Finance, and Communications, responsible for building strategic optionality for accessing capital and evaluating non-dilutive business development opportunities.
Responsibilities
Support the design and execution of Kriya's multi-path capital access strategy
Build and maintain financing scenario and valuation analyses
Evaluate non-dilutive business development opportunities
Support market intelligence and landscape analysis
Support due diligence, data-room preparation, and management presentations
Conduct literature research, scientific analysis, and scientific writing to support Foundation Medicine’s medical reporting process for cancer genomic testing.
Compensation
The expected salary range for this position based on the primary location of Boston, MA is $114,350 - $142,900 per year. The salary range is commensurate with Foundation Medicine's compensation practice and considers factors including, but not limited to, education, training, experience, external market conditions, criticality of role, and internal equity. A discretionary annual bonus may be available based on individual and Company performance.
Responsibilities
Identify, interpret, synthesize and succinctly summarize literature and other sources relevant to Foundation Medicine's comprehensive cancer genomic test.
Collaborate with internal and external scientists and physicians to review, refine, and extend existing medical content.
Generate new clinically-focused content and/or guidelines based on review of scientific literature, existing guidelines and other sources.
Contribute to the development and maintenance of Foundation Medicine's clinical oncology knowledgebase.
Contribute to additional research and development projects, both within TOCR and between departments, in support of broader TOCR and Foundation Medicine goals.
Lead the development of clinical evidence strategies and scientific documentation supporting regulatory submissions, market access initiatives, and product lifecycle decisions for medical devices.
Lead the development and execution of clinical evidence strategies for new product development and lifecycle management activities.
Manage clinical evaluation projects, ensuring alignment between clinical evidence, regulatory strategy, product claims, and commercialization objectives.
Author and maintain clinical evaluations, post-market clinical follow-up documentation, regulatory submissions, annual reports, and other clinical documentation.
Design and execute systematic literature reviews, evaluate published evidence, and synthesize clinical, preclinical, and post-market data into scientifically supported conclusions.
Assess benefit-risk profiles of medical devices and develop evidence-based recommendations in accordance with global regulatory requirements.
Requirements
Master of Science degree in a health, clinical, biological science, biomedical, engineering, or related scientific field.
Nice to have: Doctoral degree (PhD, PharmD, MD, or equivalent)
Nice to have: supporting global medical device regulatory requirements
Nice to have: Familiarity with geospatial data presentation
Nice to have: Knowledge of clean energy technologies and regulation
Nice to have: Understanding of environmental and health impacts of fossil fuel exploration and production
Latin America Scientist/Científico para América LatinaNewEarthjustice · Mexico City, Mexico
Associate Director, Corporate Strategy & Business DevelopmentKriya Therapeutics · Palo Alto, US
Medical Laboratory ScientistCentraCare · Melrose, US