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En JOB TODAY desde agosto, 2025

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2 Calle de las Eras Altas, Vallecas, 28031, Madrid, MD, Spain

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1 Seguidor

Boston Consulting Group

Research Manager - BCG Vantage

hace 3 días

Madrid

As a Research Manager within the GRO team, you will be primarily responsible for the professional development of Research Associates based in Europe. Collaborating with Research Manager peers globally to ensure excellent team coordination and strategic direction, while enabling smooth collaboration

TakeTalent

Computational Medicinal Chemist – Molecular Docking

hace 3 días

Madrid

Computational Medicinal Chemist – Molecular Docking 📍 Madrid, Spain | 💼 Full-time | 🏢 On-site About the Role TakeTalent is collaborating with PharmaMar, a leading biopharmaceutical company, to hire a talented and motivated scientist to join their R&D team with a focus on molecular docking and structure-based drug design. This is a full-time, on-site position in Madrid, offering the opportunity to contribute to early-stage discovery projects using state-of-the-art computational tools in a dynamic, multidisciplinary environment. Key Responsibilities • Design, execute, and optimize molecular docking workflows., • Analyze DNA/protein-ligand interactions, assess binding poses, calculate interaction energies, and support lead optimization., • Automate computational workflows and integrate docking data with cheminformatics libraries., • Contribute to the development and validation of new computational methodologies and pipelines. Requirements • Background in computational chemistry, bioinformatics, pharmacy, biochemistry, or a related field (MSc or PhD is a plus, but not mandatory)., • Hands-on experience with molecular docking tools and structure-based drug design., • Strong analytical skills and solid understanding of ligand-receptor interactions., • Proficiency in scripting languages and experience handling large datasets., • Excellent communication skills and a collaborative, problem-solving mindset., • Research experience or scientific publications in molecular modeling are a strong plus. What PharmaMar Offers PharmaMar fosters a dynamic and collaborative work environment where innovation drives their activities. They are strongly committed to the professional development of their employees by offering continuous training and growth opportunities. • Competitive annual gross salary + variable bonus based on goals., • Comprehensive benefits package, including on-site cafeteria, private health insurance, stock plan, and ongoing training., • A diverse, inclusive, and equal-opportunity environment. If you are passionate about research and innovation in biotechnology and meet the requirements, we look forward to receiving your application! 👉 Apply now through TakeTalent and be part of PharmaMar’s exciting journey in cutting-edge drug discovery.

Ziacom Group

Abogado/a Mercantil

hace 14 horas

Madrid

Buscamos un/a Responsable del Departamento Jurídico para incorporarse de forma estable a una compañía en pleno crecimiento. El perfil que necesitamos es el de un/a abogado/a mercantil con experiencia generalista y visión práctica orientada a aportar soluciones ágiles al negocio. Funciones principales Asesoramiento en materia mercantil: redacción, revisión y negociación de contratos de venta, proveedores, colaboración y servicios. Cumplimiento normativo: LOPD, Compliance y gestión de expedientes de reclamación. Gestión integral de temas legales de la compañía: desde renovaciones de marcas y seguimiento documental hasta la resolución de consultas legales del día a día. Interlocución directa con la Dirección General, reportando al CEO. Asumir la gestión en solitario del área legal, combinando funciones jurídicas y administrativas cuando sea necesario. Requisitos Sólida experiencia en derecho mercantil. Idiomas imprescindibles: italiano e inglés, ambos con nivel alto (fluidez en negociación). Experiencia en la gestión 360º de un departamento legal, con capacidad para adaptarse a cambios, trabajar bajo presión y cumplir con plazos exigen tes. Perfil resolutivo y práctico: orientación a soluciones útiles para la compañía, no solo a la interpretación teórica de la normativa. Disponibilidad para viajar de manera ocasional. Residencia en Madrid o posibilidad de trabajar en Pinto (Madrid) en modalidad 100% presencial. Qué ofrecemos Incorporación a una empresa consolidada y en crecimiento. Proyecto estable con responsabilidad directa en la gestión legal de la compañía. Reporte directo al CEO, con capacidad real de impacto en la organización.

Insud Pharma

Junior Data Manager

hace 14 horas

Madrid

In few wordss 📌 Position: Junior Data Manager Location: Madrid (onsite) Experience: 2-3 years of experience in data management. Extensive experience in clinical trial project data management and coordination. 👇Global Responsibility The Junior Data Manager will support the execution and monitoring of operational activities related to data management in clinical trials, working under direct supervision. They will collaborate with the study team to ensure quality and compliance of data management processes, contributing to the successful conduct of clinical projects. Specific Responsibilities • Assist all data management aspects of a clinical study with minimal oversight, including study start-up activities, and guide the study team through change orders and protocol amendments, • Assist in the development of DM documents including, but not limited to, Data Management Plans, CRFs, CRF Completion Guidelines, Edit Checks, UAT specifications, centralized monitoring plans, data flow and integrity plans, blinding plans, and data review plans. Utilize templates and standard guidelines to initiate documents, but exercise critical thinking and discretion to tailor documents to study needs, • Support to data cleaning activites such as, but not limited to, study team data reviews, Non-system Edit Check Output review, SAE reconciliation and non-CRF data reconciliation. Gather cross-functional input to create custom data review plans. Evaluate options and exercise discretion to choose efficient and effective issues resolution paths, • Demonstrate collaboration and relationship-building with all study team representatives (e.g. Biostatisticians, Statistical Programmers, Medical Monitors, Clinical Project Managers, Clinical Trial Managers, CRAs, Clinical Pharmacologists, Biomarker/Bioinformatics scientists, Medical Writers, Regulatory representatives, etc.), • Assist in manage data deliverables processes, including database locks, • Ensure data management deliverables are met on time. Utilize communication, available metrics reports, experience, knowledge, and other resources to efficiently lead and coordinate all data management activities. Ensure study team members from different functional areas understand and deliver components affecting data to ensure successful execution of deliverables. Provide solutions for data management issues that arise during study conduct, • Support on the coordination on work performed by vendors/CROs as appropriate to ensure quality of product 🤓 Competencies/Career level Innovation, customer orientation, communication, teamwork, adaptability/flexibility, productivity, Self-development, sense of urgency, initiative. Technologically savvy; quickly picks up new information Accountabilities KPI related to the job. 🕵️Requirements and personal skills • Education: Degree in Engineering, Health data or similar., • Languages: Fluent English, knowledge of other languages will be an asset., • Experience (years/area): 2-3 years of experience in data management. Extensive experience in clinical trial project data management and coordination., • Specific Knowledge: Extensive knowledge of data management and tools., • Travels: Willingness to travel occasionally., • Personal skills: Strong communication and leadership skills. Strong negotiation skills as well as excellent influencing and training/mentoring skills. Ability to focus on multiple deliverables and protocols simultaneously.