Work Schedule Standard (Mon-Fri) Environmental Conditions Office Job Description Join Us as Senior Pharmacokineticist – Make an Impact at the Forefront of Innovation We have successfully supported the top 50 pharmaceutical companies and more than 750 biotechs, spanning 2,700 clinical trials across 100+ countries in the last 5 years. As part of our expert team, you’ll have the opportunity to ensure operational excellence that makes a real difference in clinical pharmacology. As a Senior Sr Pharmacokineticist, you will oversee the clinical pharmacology and pharmacokinetic aspects of clinical trials from design through analysis and reporting. You will act as the lead pharmacokineticist on large or complex projects. Your responsibilities will include designing, analyzing, and interpreting pharmacokinetic, bioavailability, bioequivalence, and pharmacodynamic clinical trials through the analysis, interpretation, and review of pharmacokinetic and pharmacodynamic results. What You’ll Do: • Serves as Lead Pharmacokineticist or Pharmacokinetic Project Lead on large pharmacokinetic projects and/or development programs. • Manages pharmacokinetic project activities and timelines. • Serves as senior reviewer on pharmacokinetic projects. • Reviews clinical pharmacology deliverables and documents related to project activities. • Mentors Pharmacokineticist and Clinical Pharmacology staff on project activities. • Assists in staff training and professional development. • Participates in clinical pharmacology initiatives. • Develops and revises department SOPs and guidelines for the conduct, analysis and reporting of clinical pharmacology and pharmacokinetic trials. • Assists senior management team on departmental decision making, bid and marketing activities, recruitment, and process improvement. • Keeps updates on the regulatory guidelines with respect to pharmacokinetics and related disciplines and current trends. • Prepare/review Education and Experience Requirements: • Bachelor's degree or equivalent and relevant formal academic / vocational qualification • Previous experience that provides the knowledge, skills, and abilities to perform the job (comparable to 8+ years) or equivalent combination of education, training, and experience Years of experience refers to typical years of related experience needed to gain the required knowledge, skills, and abilities necessary to perform the essential functions of the job. Years of experience are not to be used as the only determining factor in establishing the job class or making employment selection decisions. Knowledge, Skills and Abilities: • Strong theoretical background in pharmacokinetics and knowledge of the drug development process • Knowledgeable of regulatory guidelines relevant to clinical pharmacology and pharmacokinetics areas of the drug development • Ability to apply pharmacokinetic theory and concepts using relevant software such as WinNonlin, NONMEM, SAS, S-Plus, R, or other pharmacokinetic packages • Hands-on experience in performing pharmacokinetics-pharmacodynamics modeling and simulation of clinical trial data is preferred • Good understanding of statistical methodology required in clinical pharmacology and pharmacokinetic trials • Proven management skills, as shown through management of multiple projects • Strong organizational skills across multiple complex projects, managing own and project team work loads, and the ability to adapt and adjust to changing priorities • Excellent written and verbal communications skills • Demonstrated initiative and motivation • Positive attitude, the ability to work well with others, and the ability of effectively mentor junior staff Working Conditions and Environment: • Work is performed in an office environment with exposure to electrical office equipment. • Occasional drives to site locations, frequent travels both domestic and international. •Exposure to fluctuating and/or extreme temperatures on rare occasions. Why Join Us? When you join Thermo Fisher Scientific, you become part of a global team that values passion, innovation, and a commitment to scientific excellence. You’ll work in an environment where collaboration and development are part of the everyday experience—and where your contributions truly make a difference. Apply today to help us deliver tomorrow’s breakthroughs.

Celerion is committed to swift, exceptional clinical research through translational medicine. Every day, we use our experience, agility, and innovative research strategies to help get drugs to market faster. We are looking for a full-time Pharmacokinetic Scientist to join our Clinical Pharmacology team. This role will be remote but linked to our Belfast, Northern Ireland site. The successful candidate must have full, permanent right to work in the UK. The Pharmacokinetic Scientist will assist with pharmacokinetic data analysis, scientific interpretation of study results, clinical report writing, and interactions with clients. Essential Functions - Data analysis and interpretation - Perform PK analyses independently - Assist with PD analyses - Interpret PK and statistical results and findings independently - Perform QC reviews as assigned - Write and review reports as assigned - Prepare PK data/report files for electronic filing of projects for submission to regulatory agencies - Maintain and file all supportive documentation pertaining to the study and ensure proper archiving of projects - Other responsibilities - Interact with clients alongside or under direction of a senior scientist, as needed - Prepare internal presentations Requirements - Master’s or PhD degree in a biology-focused sciences related field with 2+ years of related experience required - Competence in performing noncompartmental pharmacokinetic analysis with software applications such as Phoenix WinNonlin - Familiarity with processes and applications related to non-linear mixed-effect modeling and/or physiologically-based pharmacokinetic modeling is an asset - Excellent oral and written skills (English language) required Celerion is an Equal Oppourtunies employer

• Conduct independent, hands-on data analysis on RF sensor datasets using Python and Jupyter notebooks — formulating hypotheses, writing and running analytical code, interpreting results, and producing findings that directly advance program research objectives • Provide technical advice and research direction across a multidisciplinary team; define analytical objectives, review and validate technical outputs from AI/ML engineers and software developers, and ensure coherence across parallel research threads • Serve as primary technical advisor to the government sponsor: translate operational requirements into research objectives, communicate findings clearly to non-specialist stakeholders, and maintain program alignment with sponsor priorities through written reports and technical presentations • Design and execute analytical investigations into RF sensor data quality, emitter behavior, and attribution reliability — including characterizing error sources, identifying systematic artifacts, and developing methods to distinguish real physical signatures from sensor or processing artifacts • Produce technical documentation — working notes, research findings, monthly status reports, and briefing materials — that accurately represent the scope and confidence level of analytical results • Expert-level career professional recognized as a technical authority in RF systems, signals intelligence, or a closely related applied domain. Exercises broad independent judgment in defining research approach, evaluating methods, and interpreting results. Operates with minimal supervision; accountable for the scientific integrity and practical relevance of program research outputs.

• Lead the development of a next-generation video processing pipeline for DVA products • Work on architecting, coding and productizing components, features and user experiences • Conduct architecture reviews and empower teams to develop high code quality and adhere to best practices • Collaborate with a global organization of developers, product managers and designers