Role Description - Fully conversant with the trial protocol, Case Report Forms (CRFs/eCRF), off-site manual (if applicable), supporting documents, procedures, and timelines to enable day to day running of the trial including all relevant SOPs. - Communicate effectively with the Illingworth research nurse project manager (RNPM), Research nurse manager, site staff and the Principal Investigator, to ensure a smooth and efficient flow of information. - Maintain accurate documentation including electronic transfer of data as per Illingworth SOPs throughout the trial, ensuring subject confidentiality, adhering to GCP and data protection requirements. - Attend Site Initiation Visits (SIV) as required and any other necessary meetings, including multi-disciplinary, project management and client-facing meetings. - Coordinate (working with the RN team) and complete subject trial visits on- and off-site. Ensure all trial related procedures and assessments are completed according to the protocol and relevant SOPs and that data is collected accurately. - Administer trial medication as per the protocol, and facilitate the safe storage, transfer, and accountability of trial medication in accordance with Illingworth SOPs. - Process and safely package and dispatch samples, liaising with courier companies and organizations in line with project requirements and supporting documents. - Assist in identifying potentially eligible patients for research projects and assist with patient recruitment into clinical trials providing information and support for those patients for on- and off-site care. - Ensure the accurate reporting of adverse events (AEs) and serious adverse events (SAEs)/suspected unexpected serious adverse reactions (SUSARs) to the site team and relevant RNPM, providing support for any additional follow-up that may be required. - Report any suspected misconduct or fraud to Illingworth and associated companies. Qualifications - Registered nurse with a minimum of 2 years' post qualification experience. - Research and clinical trials experience with GCP certification. - Knowledge of research design and methodology desirable. - Experience and knowledge of clinical nursing skills such as Venepuncture and ECG preferable. - Ability to work autonomously with initiative in a team within a multidisciplinary environment. - Excellent verbal and written communication skills. - Ability to prioritize and manage multiple tasks. - Good working knowledge of computer software including Outlook, Word, Excel, and PowerPoint as a minimum. Company Description Illingworth Research Group provides a range of patient focused clinical services to the pharmaceutical, healthcare, biotechnology and medical device industries. These include mobile research nursing, patient concierge, medical photography and clinical research services. Illingworth are experts with experience across all study phases and in a diverse range of therapeutic areas. Illingworth Research Group is a global organization operating in over 45 countries, bringing clinical research directly into the home of the patient, to improve the experience of patients involved in clinical trials and the quality of their lives.

Role Description We're looking for an Environmental Law Research intern (32 – 40h per week) in Spain to join our Sustainability Regulatory Advisory team for a six-month internship, starting in September 2026. The internship is paid, and we occasionally hire from our intern pool. The Sustainability Regulatory Advisory team is responsible for maintaining ECOFACT Policy Outlook, our industry-leading research service on sustainability regulation. The team also advises ECOFACT’s clients on a project and mandate basis. As an Environmental Law Research Intern, you will: - Contribute to ECOFACT’s legal research on sustainability topics such as circular economy, chemicals, extended producer responsibility (EPR), packaging, and waste across 100+ jurisdictions; - Support in regulatory content creation and monitoring under the ECOFACT Policy Outlook platform and its module for pharmaceutical entities; - Be involved in the day-to-day activities of the Sustainability Regulatory Advisory team; - Contribute to other sustainability regulatory advisory projects and client deliverables on an ad hoc basis. Qualifications - Completed a Bachelor’s degree in law, international law or related field; - Pursuing a Master’s degree in disciplines such as Environmental Science, Circular Economy, Sustainability, or a related field; - Full working proficiency in English (spoken and written); - Strong document drafting skills; - High attention to detail; - Interested in environmental regulation, circular economy, and sustainability from a legal and policy perspective; - Valid Spanish work permit; - The ability to sign an internship agreement with your center of studies. Requirements - Working proficiency in other languages; - Pharmaceutical, life sciences, or chemicals industry experience; - Knowledge of, or willingness to engage with, technical aspects relevant to environmental regulation; - Familiarity with environmental regulatory frameworks specific to the pharmaceutical sector, which will be considered a strong advantage; - Strong interpersonal and analytical skills; - The ability to self-organize and deliver high quality output within short deadlines. Benefits - A great multi-national team of people who are passionate about their work and care about each other; - A respectful, non-hierarchical and politics-free working environment; - Flexible working hours; - Fully remote role; - A chance to meaningfully contribute towards the transition to a sustainable economy. Application Please apply via our job platform with your CV and a one-page cover letter in English. Reach out to Alba González at +41 58 520 20 00 with any questions that you have. Company Description At ECOFACT, we provide our clients with the knowledge required to navigate sustainability risks and regulations. By combining market-leading research with unique advisory experience, we strive to be a catalyst in the transition towards a sustainable economy. Founded in 1998 as a spin-off from a leading Swiss bank, ECOFACT is a fully independent firm headquartered in Zurich and registered in Spain. - We help our clients to understand regulatory developments in sustainability and corporate responsibility; - Build ESG risk frameworks; - Offer bespoke solutions.

Role Description We are looking for a Research Engineer to help deliver frontier-quality datasets, RL environments, and evaluations that improve state-of-the-art models for leading AI labs and enterprise clients. This is a hands-on, research-facing technical leadership role. - Work directly with customer researchers/engineers to translate their model and post-training goals into concrete data and environment specifications. - Drive the production of data that meets extremely high standards for correctness, realism, diversity, difficulty, and measurable model lift. - Operate in one or more of the following capability areas: - Coding and software engineering agents - RL environments and verifier-based training - Multimodal data and reasoning - STEM reasoning - Modern embodied AI / VLM-driven agents Qualifications - 4–5 years of experience building or improving deep learning systems where data quality mattered materially. - Strong intuition for the “data ingredients” that drive model improvements. - Ability to communicate clearly with researchers and engineers. - Demonstrated ability to be extremely detail-oriented in diagnosing subtle data quality issues. - Solid programming ability with a bias for shipping. - Python proficiency required. - Comfort with SQL/structured data workflows strongly preferred. - For coding-focused work: proficiency in one or more major languages (e.g., C++, Java, Go, Rust, JS/TS) is a plus. - Comfort designing quality systems. Requirements - Implement automated validation and filtering to achieve frontier-grade signal-to-noise. - Develop synthetic data generation and augmentation pipelines where appropriate. - Create documentation and data cards. - Design and run evaluations that reflect the customer’s intended usage. - Collaborate effectively with large production teams without being ops-heavy. Benefits - Amazing work culture (Super collaborative & supportive work environment; 5 days a week). - Awesome colleagues (Surround yourself with top talent from Meta, Google, LinkedIn etc. as well as people with deep startup experience). - Competitive compensation. - Flexible working hours.

Role Description The Research Audiologist provides clinical, scientific, and operational support for Department of Defense hearing research, auditory fitness-for-duty initiatives, hearing conservation programs, and public health activities. This position supports the planning, execution, analysis, and implementation of research and clinical programs focused on hearing readiness, operational performance, blast exposure, hearing injury prevention, and military auditory health. Remote (U.S.) with periodic travel - Personnel may perform work remotely from their residence, subject to Government approval and mission requirements. Periodic travel may be required to support research activities, clinical implementation efforts, conferences, military installations, and Government meetings. Responsibilities - Support execution of IRB-approved research protocols. - Conduct advanced audiometric and functional hearing assessments. - Support development and validation of auditory fitness-for-duty assessment methodologies. - Participate in blast exposure, hearing performance, and hearing conservation research studies. - Collect, analyze, and interpret audiological, clinical, and research data. - Support implementation of hearing conservation initiatives and hearing readiness programs. - Collaborate with clinicians, engineers, researchers, and Government stakeholders. - Prepare technical reports, presentations, manuscripts, and scientific briefings. - Support tele-audiology and clinical technology implementation efforts. - Assist with evaluation of emerging hearing technologies and operational hearing assessment tools. Qualifications - Possess excellent written and verbal communication skills. - Possess knowledge of Microsoft Office applications. - Possess excellent ability to manage multiple tasks with competing deadlines. Requirements - Doctor of Audiology (Au.D.) or Ph.D. in Audiology. - Minimum two (2) years of clinical and research audiology experience. - Travel as required to support research, training, and public health initiatives. - U.S. Citizenship required. - Ability to obtain and maintain a favorable Government suitability determination. - Ability to obtain and maintain SECRET clearance if required. Preferred Qualifications - Experience supporting DoD, VA, or Military Health System programs. - Experience conducting human-subjects research under IRB protocols. - Experience supporting hearing conservation and hearing readiness programs. - Knowledge of auditory fitness-for-duty (AFFD) concepts. - Experience with speech-in-noise testing and functional hearing assessments. - Experience with blast exposure, tinnitus, hearing injury, or auditory-vestibular research. - Experience analyzing epidemiological, longitudinal, or clinical datasets. - Experience with tele-audiology technologies. - Experience presenting scientific findings and preparing manuscripts. - Experience supporting geographically dispersed teams, hybrid work environments, remote operations, or nationwide field activities. - Preferred candidates will have current or prior experience supporting the Defense Health Agency (DHA), Hearing Center of Excellence (HCE), National Military Audiology and Speech Pathology Center (NMASC), Defense Centers for Public Health (DCPH), Military Health System (MHS), Veterans Health Administration (VHA), military treatment facilities (MTFs), hearing conservation programs, auditory readiness initiatives, or other military health and public health programs. Benefits - The salary range for this position is $105,000.00 to $135,000.00 annually. - Competitive base salary commensurate with qualifications and experience. - Comprehensive benefits package, including medical, dental, and vision insurance. - 401(k) plan with company matching. - Tax-deferred savings options. - Supplementary benefits. - Paid time off. - Professional development opportunities.