pstrong TakeTalent /strong joins strong PharmaMar i /strong n the search for a strong Clinical Pharmacology Scientist /strong to support the development of innovative oncology therapies through cutting-edge strong clinical pharmacology /strong and strong model-informed drug development strategies /strong . /pbr¿Todo listo para enviar su solicitud? Asegúrese de comprender todas las responsabilidades y tareas asociadas a este puesto antes de continuar.brp At strong PharmaMar /strong , they are committed to advancing science and transforming patient outcomes through innovative oncology research. The Clinical Pharmacology team plays a critical role in early clinical development, generating the pharmacokinetic, pharmacodynamic and translational insights needed to optimize drug development and support regulatory decision-making. /ppb What will you do? /b /pp• Support the implementation of Clinical Pharmacology and Early Clinical Development plans with scientific rigor and a high level of autonomy. /pp• Provide guidance and scientific mentorship to Clinical Pharmacology Scientists and Associate Scientists within the team. /pp• Coordinate and oversee bioanalytical activities, including sample shipment tracking, vendor management, review of validation plans, budgets and work orders. /pp• Perform pharmacokinetic analyses, including Non-Compartmental Analysis (NCA), Population Pharmacokinetic (PopPK) analysis and Physiologically Based Pharmacokinetic (PBPK) modeling. /pp• Conduct pharmacodynamic and PK/PD analyses to assess treatment efficacy, dose-limiting toxicities and exposure-response relationships. /pp• Support first-in-human (FIH) studies, including ECG/Holter monitoring activities and c-QT/t-QT analyses.



/pp• Contribute to Model-Informed Drug Development (MIDD) initiatives through pharmacometric analyses, simulations and interpretation of results. /pp• Develop and maintain high-quality analytical workflows and databases following Good Coding Practices. /pp• Contribute to Clinical Pharmacology sections of study protocols, development plans, scientific publications and technical reports. /pp• Provide scientific support to Regulatory Affairs activities and interactions with agencies such as the EMA and FDA. /pp• Collaborate closely with cross-functional teams including Medical Oncology, Biostatistics, Data Management and other key stakeholders. /pp• Participate in departmental initiatives that contribute to the overall success of Early Clinical Development programs. /ppb Position requirements /b /pp• Bachelor’s degree in strong Pharmacy, Medicine, Biology, Biotechnology /strong or a related scientific discipline. /pp• Master’s degree and PhD in strong Pharmacology /strong , Immunology, Computational Biology, Bioinformatics, Biostatistics or a related field. /pp• Fluent English, both written and spoken. /pp• More than 3 years of experience in clinical research, preferably within pharmacology, immunology or translational medicine. /pp• Experience authoring scientific publications and technical reports. /pp• Proven expertise in pharmacometric modeling tools such as b NONMEM,



Monolix, PK-Sim or similar platforms. /b /pp• Strong programming skills in R and SAS for data analysis and process automation. /pp• Knowledge of additional programming languages such as Python and Bash. /pp• Experience in bioanalysis and biomarker evaluation. /pp• Solid understanding of statistical methodologies, including descriptive, univariate and multivariate analyses. /pp• Experience with strong Next-Generation Sequencing /strong(NGS), pharmacogenetics, genotyping analyses and bioinformatics pipelines. /pp• Excellent communication skills and the ability to work independently while contributing effectively within multidisciplinary teams. /ppb What do we offer? /b /pp• Competitive annual salary and performance-based bonus. /pp• Comprehensive benefits package, including private health insurance, employee share plan, company canteen, continuous training and development opportunities, among others. /pp• Adaptable start time (7:30h to 9:30h) and intensive working hours on Fridays. /pp• Hybrid working model available after successfully completing the six-month probation period, combining on-site collaboration with remote work flexibility. /pp• The opportunity to contribute to groundbreaking oncology research in an innovative and science-driven environment. /pp• A strong commitment to diversity, equal opportunities and an inclusive work environment where all talent is valued and respected. xsgfvud /ppb If you are passionate about clinical pharmacology, translational science and innovative drug development, we would love to hear from you. /b /pbrHay opciones de teletrabajo/trabajo desde casa disponibles para este puesto.

📌 Clinical Pharmacology Principal Scientist (Alcobendas)
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📍 Alcobendas