Empleos de ich en Barcelona

Jobtailor in Barcelona, Spain, is seeking an experienced Medical Writer to compile and coordinate clinical documents, ensuring adherence to ICH E3 guidelines and regulatory standards.You will review study protocols, clinical study reports, manuscripts, and investigator brochures, manage editorial reviews, and collaborate with clients and internal teams to...

Job descriptionYour mission The Senior Analytical Development Manager will be responsible for leading and managing Analytical Development activities within the Pharmaceutical Development Department. In this role, you will lead a team of Junior and Senior Scientists and Analysts, providing scientific and strategic direction across the analytical...

The Global Study Associate Director (GSAD) is a business-critical role within Study Management, BioPharmaceuticals Clinical Operations, whose main accountability is the delivery of clinical studies. The GSAD is responsible for leading a cross-functional study team and for providing the team with direction and guidance to enable successful study delivery. The...

Responsibilities (a) Site management • Study site selection, initiation (SIV) and clinical monitoring. • Perform pre-study visit to ensure eligible sites are selected according to sponsor site selection criteria, including but not limited to adequate resources and experience. • Prepare and conduct SIV to ensure adequate study training for relevant...

Are you ready to orchestrate complex, global oncology studies that accelerate lifesaving medicines to patients? In this role, you will connect scientific ambition with disciplined execution, ensuring pivotal trials move from protocol to meaningful results with speed, rigor and care. You will partner across internal functions and world-class external...

About this roleTFS HealthScience is a leading global mid-size Contract Research Organization (CRO) that partners with biotechnology and pharmaceutical companies throughout their entire clinical development journey. Our expertise includes full-service capabilities, resourcing, and Functional Service (FSP) solutions.The Drug Safety Associateis part of the...

Clinical Data Engineer CDP & DP Main PurposeDrives the setup and maintenance of clinical data collection instrument(s), data ingestion and integration capabilities from all study data sources (sites and vendors – labs, IRT, ePRO, digital devices, etc.), based on the Clinical Study Protocol and Medical Standards in collaboration with the study team and...

IQVIA Biotech is hiring Clinical Research Associate in Spain!IQVIA Biotech partners exclusively with biotech and emerging biopharma companies to support clinical development across all phases and therapeutic areas. agile structure, collaborative culture, and deep therapeutic expertise allow us to deliver tailored solutions that help bring innovative...

CRA IIICON is a global healthcare intelligence and clinical research organisation united by a mission to bring new medicines and treatments to patients faster.As a values-driven organisation, integrity, collaboration, agility, and inclusion are at the heart of how we work and interact with each other, customers, patients and suppliers.We are currently...

Your MissionWe are scientists, doctors, techies and humanity lovers, with the mission of pioneering real time precision neurology to cure brain-related disorders. INBRAIN harnesses the extraordinary material properties of Graphene, the world’s thinnest and nobel-prize winning material, to build high resolution neural systems. Our mission is to decode and...

Join Our Talent CommunityWe're not advertising a specific role today - we're proactively connecting with experienced professionals for upcoming opportunities. As part of ourteam, you would be working alongside passionate and innovative professionals to ensure our customers achieve their goals. By joining our talent community, you'll be among the first...

Gestionar estudios clínicos globales, asegurando entregas a tiempo y dentro del presupuesto, con experiencia en regulaciones ICH-GCP y entornos matriciales.

Join Our Talent CommunityWe're not advertising a specific role today - we're proactively connecting with experienced professionals for upcoming opportunities. Who We're Looking to Connect WithExperienced Data Managers with a background in clinical research and drug developmentPrincipal, Lead, or Senior Data Managers seeking their next challengeProfessionals...

We are looking for a Manager specialized in SAP EWM. If you thrive working in a fast-paced environment, working with industry leading clients, moving frequently from project to project to solve significant business challenges… then, we’d like to meet you!What you will do:As a Manager in the Fulfillment team (Supply Chain & Operations), you will lead...

Join Our Talent CommunityWe're not advertising a specific role today - we're proactively connecting with experienced professionals for upcoming opportunities. Who We're Looking to Connect WithExperienced Data Managers with a background in clinical research and drug developmentPrincipal, Lead, or Senior Data Managers seeking their next challengeProfessionals...

Join Our Talent CommunityWe're not advertising a specific role today - we're proactively connecting with experienced professionals for upcoming opportunities. Who We're Looking to Connect WithExperienced Data Managers with a background in clinical research and drug developmentPrincipal, Lead, or Senior Data Managers seeking their next challengeProfessionals...

Study Site Specialist – Spain We are seeking an experienced Study Site Specialist to join a global clinical res Search programme. This is a permanent, fully remote position for candidates based in Spain. Location: Spain Working arrangement: Fully remote Employment type: Permanent Position Summary The Study Site Specialist will manage site start-up...

ICON busca un Global Study Manager para integrarse en el equipo de operaciones clínicas, gestionando estudios clínicos globales y asegurando entregas a tiempo y dentro del presupuesto. Se requiere título en ciencias de la vida, 5+ años en investigación clínica y 3+ años en gestión de proyectos globales, con conocimiento de regulaciones ICH-GCP; ...

Are you ready to join a world leader in the exciting and dynamic fields of the Pharmaceutical and Medical Device industries? PQE Group has been at the forefront of these industries since 1998 , with 40 subsidiaries and more than 2000 employees in Europe, Asia and the Americas. We are currently seeking an experienced Commissioning, Qualification & Validation...

Are you ready to join a world leader in the exciting and dynamic fields of the Pharmaceutical and Medical Device industries? PQE Group has been at the forefront of these industries since 1998 , with 40 subsidiaries and more than 2000 employees in Europe, Asia and the Americas. We are currently seeking an experienced Commissioning, Qualification & Validation...