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Purpose We are seeking a highly experienced Linguistics professional consultant to serve as a consultant on AI training data projects for leading AI model builders and enterprises. Your focus will be to define success criteria, review outputs, and provide targeted guidance to improve quality and speed — directly contributing to the successful delivery of domain-specific annotated datasets that meet the highest technical standards. You will be engaged on specific projects with clearly defined deliverables, milestones, and end dates. Components Technical Standard Setting, Quality Control, and Process Improvement • Define domain-specific quality success metrics (e.g., accuracy of transcription, consistency in linguistic annotation schemes, phonetic transcription accuracy, adherence to grammatical frameworks, correct use of linguistic markup standards such as IPA or Universal Dependencies)., • Develop project-specific SOPs, QA rubrics, and reference materials for the specific purpose of meeting client technical standards., • Review project outputs (transcriptions, annotations, language datasets) against technical standards, flagging and correcting defects before client delivery., • Perform structured QA passes on daily/weekly deliverables; flag, track, and resolve defects quickly to hit delivery deadlines., • Return work to contractors with precise remediation notes., • Provide advisory input on tools, workflows, and processes to meet quality benchmarks., • Handle spec changes and edge-case scenarios — e.g., annotation of rare dialects or ambiguous language constructs — drafting acceptance criteria or workarounds., • Curate example libraries of “gold standard” linguistic data for calibration and comparability to agreed reference samples. Talent Vetting & Output Improvement • Participate in vetting and assessing technical contractor talent for specific projects, including transcription accuracy tests and linguistic annotation evaluations., • Review sample work from contractors and provide precise, actionable written feedback to improve outputs., • Create targeted training or calibration resources — e.g., phonetic transcription guidelines, morphological analysis instructions, disambiguation procedures. Project Delivery Support • Advise on technical scoping and requirements during project setup, including selection of annotation frameworks and language coverage specifications., • Provide expert guidance for edge cases, technical exceptions, and specification changes., • Contribute to post-project reviews to capture lessons learned and improve future standards., • Identify and summarize client model observations and insights (e.g., frequent misannotations, language-specific bias patterns)., • Build dashboards or trackers with defect categories and recurrence to surface production insights that improve project outcomes., • Conduct post-mortems, analyze defect trends, and propose process tweaks or training refreshers. Target Profile • Advanced degree (ideally PhD) in Linguistics, Applied Linguistics, or a closely related field, with demonstrable research or industry impact., • 5+ years professional expertise in linguistic analysis, annotation standards, and language data quality control., • Proven ability to set, enforce, and maintain high technical standards in linguistic data creation projects., • Strong communication skills for delivering clear technical guidance., • Experience producing technical documentation, quality rubrics, or training resources., • Ability to work within fixed project timelines and scope., • Strong attention to detail, documentation discipline, and commitment to accuracy and consistency., • Fluency in spoken and written English, with additional language proficiency preferred. Example Data Annotation - Potential Scope Field of Study Agent Task Specialty Linguistics Register/genre fit enforcement, dialect fidelity, orthography consistency Sociolinguistics Dialect/register policy setting, code-switch handling Phonetics & Phonology Transcription accuracy, disfluency policy, prosodic annotation Applied Linguistics Script/orthography/romanization standards, tokenization Computational Linguistics Named entity handling, punctuation conventions Corpus Linguistics Metadata completeness, defect tracking, IAA monitoring Translation & Localization Policy compliance checking, edge-case arbitration Language Technology Validator creation (regex/scripts), automation of QA checks Psycholinguistics Prompt/script design, scenario coverage Language Documentation Gold-standard library curation, reviewer calibration Language Studies Multiscript/multimodal transcription QA We offer a pay range of $25-to- $100 per hour, with the exact rate determined after evaluating your experience, expertise, and geographic location. Final offer amounts may vary from the pay range listed above. As a contractor you’ll supply a secure computer and high‑speed internet; company‑sponsored benefits such as health insurance and PTO do not apply. Job title: Linguistics Expert (SME) Employment type: Contract Workplace type: Remote Seniority level: Senior Level

Overview Certara: Certara (CERT) is the largest and most comprehensive provider of strategic drug development, modeling & simulation and regulatory science services. We partner with biopharmaceutical businesses to optimize drug development decisions and accelerate the drug development process. At Certara, you will play an important role helping our clients develop new therapies and target unmet medical needs, expand the benefits of existing therapies to other populations, communicate scientific information in the language of regulatory success, balance risk profiles, differentiate drugs from a competitive perspective, and unlock millions in R&D savings. Ultimately, you’ll be helping more critical drug products get to more patients. Regulatory Writers prepare high quality documentation for regulatory submissions in order to help streamline the regulatory approval process for our clients. The Associate Principal Regulatory Writer (APRW) is a major contributor to document authorship for a variety of clinical documents across different therapeutic areas. The APRW will be the project lead on smaller projects, interfacing directly with the client, but also support larger, more complex engagements as a member of a larger delivery team. Responsibilities Responsibilities • Work closely with client and internal and partner organization teams to lead development of strategies for organizing and preparing regulatory documents, • Lead a project team, and actively participate in development and writing of high-quality documents (study-level and submission level documents, pharmacovigilance documents), • Author documents per client specifications, templates, style guides, and other guidance documents, • Author documents per regulatory authority guidelines and requirements, • Act as client advisor, working collaboratively and developing a strong relationship of trust built upon consistent and reliable communication; communicate ideas and strategies to produce a successful end result, • Practice blameless problem solving, taking broad perspectives in resolving issues to prevent negative impact to work, • Manage budget for a low complexity project, including all contributors (writers, editors), • Usher documents through the review process, conduct comment resolutions meetings (CRMs) and successfully lead a project team to consensus, • Maintain collaborative, proactive, and effective communication with both client and internal teams, • Lead project-related meetings and teleconferences, • Provide coaching to junior staff for study level documents as well as submission level documents and ensure all staff comply with company standard operating procedures (SOPs) and training requirements Qualifications Qualifications • Education, Experience, Training, and Knowledge:, • Bachelor’s degree; MS or PhD preferred, • 5-8+ years of regulatory writing experience or equivalent experience with clinical sections of the CTD such as:, • 2.5 Clinical Overview, • 2.7 Clinical Summaries, • Clinical Study Reports, • Clinical Study Protocols, • Briefing Documents, • Understand regulatory authority guidelines and requirements to be able to lead an internal project team and anticipate the effects that writing practice conventions can have on the final product when seeking health authority approval/acceptance, • Intermediate proficiency with Microsoft Word skills (editing tools, creating and modifying tables and inserting figures) and document management techniques, • Strong understanding of the document creation process and of the drug development lifecycle, • Able to synthesize data across multiple data sources and documents to create summary reports, • Expertise to provide subject matter guidance for quality document preparation, document review, accurate comment resolution/incorporation, and document finalization, • Ability to own submission-level sections (e.g., clinical section [Module 2.7]), taking responsibility for clarity of purpose, leading others toward the common goal within timeline and budget on complex projects, • Demonstrate an understanding of communication best practices, coaching others on communication implications of decision making, • Develops professional relationships with clients as a way to further the business relationship and maintain current industry knowledge, • Ability to identify and institutionalize work practices that are most effective in order to ensure consistency in performance, • Ability to resolve problems that arise, particularly in sensitive or high-pressure situations, • Possesses broad experience and technical expertise across more than one therapy area and integrates this knowledge to deliver business successes and actively transfer this knowledge to strength the skill base across the organization EEO Certara bases all employment-related decision on merit, taking into consideration qualifications, skills, achievement, and performance. We treat all applicants and employees without regard to personal characteristics such as race, color, ethnicity, religion, sex, sexual orientation, age, nationality, marital status, pregnancy, physical or mental condition, genetic information, military service, or other characteristic protected by law.

Title: Data Partner - Business Writer - French Location: Global - Remote Are you ready to use your domain knowledge to advance AI? Join us as a Data Partner and work remotely with flexible hours. We are seeking highly knowledgeable Subject Matter Expert to design advanced, domain-specific questions and solutions. The role involves creating challenging problem sets that test deep reasoning and expertise in the assigned field. TELUS Digital AI Community Our global AI Community is a vibrant network of 1 million+ contributors from diverse backgrounds who help our customers collect, enhance, train, translate, and localize content to build better AI models. Become part of our growing community and make an impact supporting the machine learning models of some of the world’s largest brands. Key Responsibilities: • Develop complex, original question-and-answer pairs based on advanced topics in your area of expertise., • Ensure questions involve multi-step problem-solving and critical thinking., • Provide detailed, clear solutions that meet high academic standards., • Collaborate with cross-functional teams to refine and enhance content. Qualification path: Basic Requirements: • A completed PhD, Master’s, or Bachelor’s degree in Business Writing is essential., • Strong proficiency in French writing with excellent grammar, clarity, and the ability to explain complex concepts concisely. Assessment: In order to be hired into our community, you’ll go through a subject-specific qualification exam that will determine your suitability for the position and complete ID verification. Equal Opportunity: All qualified applicants will receive consideration for a contractual relationship without regard to race, color, religion, sex, sexual orientation, gender identity, national origin, disability, or protected veteran status. At TELUS Digital AI, we are proud to offer equal opportunities and are committed to creating a diverse and inclusive community. All aspects of selection are based on applicants’ qualifications, merits, competence, and performance without regard to any characteristic related to diversity.

About us Plessey has a long history of innovation. Founded in 1956, we have evolved from one of Europe’s earliest semiconductor pioneers into the world’s most advanced microLED specialist. Over the decades, Plessey has built a first class, fully integrated platform designing, manufacturing, and engineering next-generation display technologies entirely in-house. This end to end capability, combined with our strong IP portfolio, uniquely positions us to lead the scaling of MicroLEDs from lab innovation to high-volume production. Our future is even brighter. We believe MicroLEDs will define the next era of technology—powering ultra-efficient AR/VR displays, driving optical processors that make AI faster and more sustainable, and enabling devices yet to be imagined. With our unique expertise and talented team, we are positioned to lead this transformation. It’s an exciting time to join us: Plessey has recently been acquired by Haylo Labs, accelerating our growth and opening new opportunities. Our Values • Innovation, • Collaboration, • Commitment, • Care Location Based at our manufacturing facility in Plymouth, UK. About the Role We are seeking an experienced and innovative Team Lead for Films Technology to drive the development, optimisation, and integration of thin-film processes for advanced MicroLED display devices. This role oversees end-to-end technology development, including epitaxial layers, passivation films, optical coatings, buffer layers, and functional thin films critical to MicroLED performance, yield, and reliability. The ideal candidate has strong technical depth in semiconductor materials and thin-film engineering, along with proven leadership experience in guiding cross-functional teams. Key Responsibilities • Drive process innovation to enhance device efficiency, reliability, uniformity, and surface quality, • Take ownership of deposition process modules (PVD, ALD, PECVD, sputtering, evaporation, plating) and ensure stable, high-quality film performance, • Work closely with epitaxy, device, and integration teams to define film requirements and deliver optimised stack architectures, • Establish and refine process windows through DOE, SPC, and data-led analysis, • Identify and resolve thin-film defect mechanisms such as particles, stress, adhesion, moisture ingress, and interface issues, • Support reliability engineering by assessing film stability under thermal, optical, electrical, and environmental stress, • Utilise advanced metrology (SEM, TEM, AFM, ellipsometry, XRR, XPS, SIMS, etc.) to ensure film quality and process control, • Act as Tool Owner for assigned equipment, maintaining tool performance, uptime, safety, and accurate documentation, • Lead continuous improvement initiatives to reduce downtime, enhance tool capability, and troubleshoot complex tool or process issues, • Provide day-to-day leadership to the module team, including line management of Apprentices, Graduates, Engineers, and Senior Engineers, • Conduct performance reviews, set objectives, and support the technical and professional development of team members, • Oversee resource planning to ensure effective deployment of personnel, equipment, and expertise across projects, • Collaborate with the Module Manager to align team activities with broader project and company objectives Experience & Attributes • Master’s or PhD in Materials Science, Electrical Engineering, Applied Physics, or a related discipline, • Significant industry experience (7+ years) in thin-film engineering within the semiconductor industry, • Practical expertise in thin-film deposition (PVD, ALD, PECVD, MOCVD, sputtering, evaporation), • Strong background in microfabrication and device process integration, • Proven experience leading engineers, projects, or technical teams, • Demonstrated tool ownership, • Strong technical judgement and decision-making skills, • Effective cross-functional communication and collaboration, • Excellent problem-solving skills, particularly in ambiguous or fast-moving environments, • Ability to prioritise and deliver within tight development cycles, • Strategic thinker with the ability to plan roadmaps and guide technology direction Advantage • Experience with GaN-based device processing and characterisation, • Good understanding of MicroLED device architecture, materials challenges, and reliability mechanisms, • Previous line management experience, • Knowledge of optical coatings and light-management films used in display devices, • Familiarity with high-volume manufacturing (HVM) processes and scaling challenges, • Experience in defect engineering, surface passivation, or interfacial film optimisation

Director - RWE/Epidemiology Remote based (UK) A rare opportunity to join a mid-sized, highly scientific, international healthcare consultancy providing a range of innovative services to Life Sciences companies. You will have solid foundations and a flowing book of business to build from. I am looking for an experienced epidemiologist comfortable with leading studies end to end, mentoring and managing a small team of juniors and playing a supporting role in BD/client management. Combining both traditional and novel analytical approaches with diverse real-world data, including genomic, medical record, claims and patient-reported information, has allowed my client to inform Life Sciences/Pharma company internal decision making as well as submissions and presentations to regulators; health technology assessment authorities and payers; the medical community; and, patient organizations. The Epidemiology team and this position: The Epidemiology team consists of scientific experts who lead study design, methodology development and result interpretation across a broad range of RWE/HEOR studies, for the pharmaceutical industry. The professional in this position will demonstrate a passion for the generation of rigorous and relevant RWE, ensuring delivery of high-quality evidence and outputs. The Director, Epidemiology, will independently drive study design, oversee data analysis and interpretation, and lead collaboration with clients and cross-functional teams. This individual will play a key role in advancing the organization’s epidemiologic and real-world data capabilities and supporting high-impact evidence generation for regulatory, clinical, and commercial use. Accountabilities within this role: • Lead and refine epidemiological study designs, addressing complex methodological challenges., • Oversee protocol development, analysis plans, and study reports ensuring clarity and quality., • Interpret results independently and communicate findings effectively to clients and stakeholders., • Apply deep therapeutic and coding expertise to align study design with data needs., • Utilise advanced knowledge of real-world data sources to guide study feasibility and interpretation., • Lead cross-functional teams and mentor junior epidemiologists., • Drive innovation and contribute to scientific thought leadership., • Manage multiple projects, ensuring timely, high-quality deliverables., • Support business development through proposal leadership and client engagement. Ideal profile: • MSc or PhD in Epidemiology, • 6+ years of Epidemiological research experience, with substantial RWE focus in consulting, pharmaceutical or biotech settings (previous private sector/consulting experience desirable, but strong senior academic candidates considered), • Experience working with US and UK data sets is desirable (secondary data, claims, EHRs, etc.), • Proven leadership in study design, client interaction, and team management., • Deep expertise in epidemiological methodologies, therapeutic areas, and medical coding., • Strong record of scientific communication, including authorship and presentations., • Excellent interpersonal skills for mentoring, collaboration, and client engagement., • Exceptional organisational skills and attention to detail, • Flexibility to adapt to client project needs and handle competing priorities in a fast-paced workplace Competitive base salary, annual performance bonus and strong benefits package on offer. Don't miss out on this rare opportunity to join a close-knit, people focused company going through an exciting growth phase, becoming one of the leading specialist consulting teams in the RWE/HEOR space. Apply or reach out now for more information -

We are currently recruiting for an experienced, driven and passionate Statistician to join our FSP Team at Principal level. This position can be fully remote, although can be office or hybrid (depending on the candidate's location). Responsibilities As a Principal Statistician you will work on assigned studies within the team for one of our global pharmaceutical clients. You will hold a combined hands on technical and project leadership role, where you will be a key member of the FSP team and a key point of contact for the client. You will contribute to, and/or lead, the statistical components of deliverables; ensuring all are produced to excellent quality whilst adhering to deliverable timelines. You will be responsible and accountable for assigned statistical and programming aspects of reporting, as well as engage in internal and external knowledge exchange activities and provide support to colleagues. You will oversee junior colleagues and there may be the opportunity to line manage as you progress within your role. The successful candidate should have experience doing the following: • Leading clinical studies, including providing statistical leadership on methods and managing relationships with vendors, • Advising on and performing ad hoc analyses such as those required for publications, • Strong programming skills in SAS and/or R Qualifications The successful candidate should have obtained and have experience in the following: • PhD or MSc in Biostatistics or related discipline, • Experience within the pharmaceutical industry to have a good awareness of clinical trial issues, design, and implementation, • Familiarity with GCP and regulatory requirements, • Good exploratory analysis and data visualization skills, • Cross-functional experience (e.g. collaborating closely with Medical / Clinical / other functions on exploratory analyses for publication purposes, i.e. abstracts & posters for medical congresses, manuscripts, etc.), • Strong SAS and/or R programming experience Why Join Us • Remote working and flexible working hours, • Career development, mentorship, and continuous learning, • Supportive, friendly, and collaborative culture, • Making a Positive Impact: As a B-Corp™ organization, we are committed to sustainability, solid responsibility and strong ethical governance through our ESG initiatives About Phastar Phastar is an award-winning biometrics and data science CRO, trusted by pharma, biotech, and medical device companies worldwide. With a global team of data specialists, we bring expertise, precision, and pace to every trial, because behind every data point is a patient waiting for treatment. We transform complex data into clear, actionable intelligence, helping accelerate drug development, and bring life-changing therapies to patients faster. Awards & Recognition • SCRIP – Best Contract Research Organization, Specialist Provider, • Citeline – 2025 Award Winner, • Fierce CRO Awards – Recognized Industry Leader Apply Now Be part of a team known for technical expertise, quality, and impact. We value Excellence, Collaboration, Integrity, Innovation, and Passion—and we seek team members who embody these qualities. Apply today! Phastar is committed to the principles and practices of equal opportunities and to encourage the establishment of a diverse workforce. It is our policy to employ individuals on the basis of their suitability for the work to be performed and their potential for development, regardless of age, sex, race, color, nationality, ethnic or national origin, disability, marital status, pregnancy or maternity, sexual orientation, gender reassignment, religion, or belief. This includes creating a culture that fully reflects our commitment to equal opportunities for all. Important notice to Employment businesses/Agencies Phastar does not accept referrals from employment businesses and/or employment agencies in respect of the vacancies posted on this site. All employment businesses/agencies are required to contact Phastar's Head of Talent Acquisition to obtain prior written authorization before referring any candidates to Phastar. The obtaining of prior written authorization is a condition precedent to any agreement (verbal or written) between the employment business/ agency and Phastar. In the absence of such written authorization being obtained any actions undertaken by the employment business/agency shall be deemed to have been performed without the consent or contractual agreement of Phastar. Phastar shall therefore not be liable for any fees arising from such actions or any fees arising from any referrals by employment businesses/agencies in respect of the vacancies posted on this site.

A leading technology solutions provider is seeking a Subject Matter Expert with a PhD in Bioinformatics, Mathematics, Chemistry, or Physics.

Coastal Ocean Modelling Scientist – National Oceanography Centre. Experience in dynamical environmental modelling, preferably in oceanography. Strong 1st degree in a numerate science, engineering or mathematics discipline and PhD or equivalent research experience in physical oceanography or other