20 publicaciones de empleo destacadas de de farmacia en sabadell, ct (¡Están contratando!)

Associate Clinical Study Excellence Scientist
Bayer —Barcelona, Barcelona provincia
- Doctorado
- Sin necesidad de experiencia
- Investigación
9d
Training Specialist
Instituto Grifols SA —Parets del Vallès, Barcelona provincia
- Jornada completa
- Microsoft Office
- Grado
- Habilidades organizativas
- Formación continua
- Flexibilidad horaria
Técnico de PPWR - 40h - Barcelona
Miin Cosmetics —Barcelona, Barcelona provincia
- Jornada completa
- Trabajo híbrido
- Inglés
- Máster
- Grado
Solicitud rápida
10d
QA Operations Specialist
Biomat SA —Parets del Vallès, Barcelona provincia
- Jornada completa
- Inglés
- Microsoft Office
- Máster
12d
ANALISTA DE LABORATORIO DE FISICOQUÍMICO (CERT. DISCAPACIDAD)
Fundación Esclerosis Múltiple —Corbera de Llobregat, Barcelona provincia
- De 25.000 € a 27.000 € al año
- Español
- Formación continua
12d
Senior Scientific Writer
Sanofi —Barcelona, Barcelona provincia
- Inglés
- Habilidades de comunicación
Regulatory Affairs Technician (LATAM) – Badalona
Menarini —Badalona, Barcelona provincia
- Jornada completa
- Trabajo híbrido
- Inglés
- Grado
Validation Technician
Grifols SA —Parets del Vallès, Barcelona provincia
- Jornada completa
- Trabajo híbrido
- Inglés
- Project management
- Grado
Farmacèutic/a Especialista en Farmàcia Hospitalària - Assajos Clínics (ICO Hospitalet)
Institut Català d'Oncologia —l'Hospitalet de Llobregat, Barcelona provincia
- Jornada completa
- Español
- Hospital
TECHNICAL DRUG SAFETY OFFICER
Instituto Grifols SA —Sant Cugat del Vallès, Barcelona provincia
- Jornada completa
- Trabajo híbrido
- Microsoft Excel
- Inglés
- Máster
3d
MANIPULADORES/AS FARMACEUTICOS/AS
DIFARMED SLU —Sant Feliu de Llobregat, Barcelona provincia
- Desde 1.743 € al mes
- Jornada completa
Solicitud rápida
Farmacéutico/a Sustituto/a
Farmacia Ruth Calvo Sanchez —La Llagosta, Barcelona provincia
- Grado
Solicitud rápida
11d
Quality Program Associate
Aizon —Barcelona, Barcelona provincia
- Jornada completa
- Trabajo híbrido
- Español
- Informática
- Inglés
- Seguro dental
Solicitud rápida
Docente Higiene Bucodental Barcelona
Sanitas —Barcelona, Barcelona provincia
- Medicina
- Inglés
- Enfermería
Solicitud rápida
plaça de Tècnic assistencial de Salut a la Regió Sanitària Barcelona Ciutat (Barcelona) CIDO
Consorci Sanitari de Barcelona —Barcelona, Barcelona provincia
- Enfermería
8d
Pharmacokinetic Scientist
Kymos Group —Barcelona, Barcelona provincia
- Español
- Doctorado
- Inglés
10d
Commercial & Academic Clinical Research Director
VHIR —Barcelona, Barcelona provincia
- Jornada completa
- Trabajo híbrido
- Español
- Doctorado
- Hospital
Expert Scientific writer HEVA
Sanofi —Barcelona, Barcelona provincia
- Inglés
- Habilidades de comunicación
Regulatory & Packaging Sustainability (C. Formativo)
Miin Cosmetics —Barcelona, Barcelona provincia
- Jornada completa
- Inglés
- Máster
- Grado
- Formación continua
Solicitud rápida
10d
QA R&D Technician (Temporal)
Synthon Hispania —El Prat de Llobregat, Barcelona provincia
- De lunes a viernes
- Inglés
- Máster
- Grado
- Flexibilidad horaria

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Associate Clinical Study Excellence Scientist

Bayer -
Barcelona, Barcelona provincia

Solicitar ahora

Detalles del empleo

Hace 9 días

Cualificaciones

Investigación clínica
Doctorado
Sin necesidad de experiencia
Investigación
MRP
UAT
Farmacia

Descripción completa del empleo

At Bayer we’re visionaries, driven to solve the world’s toughest challenges and striving for a world where ,Health for all, Hunger for none’ is no longer a dream, but a real possibility. We’re doing it with energy, curiosity and sheer dedication, always learning from unique perspectives of those around us, expanding our thinking, growing our capabilities and redefining ‘impossible’. There are so many reasons to join us. If you’re hungry to build a varied and meaningful career in a community of brilliant and diverse minds to make a real difference, there’s only one choice.

Associate Clinical Study Excellence Scientist

Purpose

The Assoc. CSES is a member of the core study team. The role will serve as a key liaison for the medical aspects of a trial within the study team. It encompasses ensuring the quality and integrity of medical study data and optimization of drug development within the trial's framework. The Assoc. CSES supports the CSES or works independently in less complex trials.

Geographical Scope

Global

Key Responsibilities

You will perform medical oversight of CD&O clinical trials and ensure participant safety and scientific integrity of the study from concept to final report. You can be the clinical representative in the core study team. In this role, you:

Contribute to the medical sections of the study protocol and other study documents
Provide input for the medical sections of clinical study reports and annual report documentation
Perform medical review and analysis of safety data to detect trends and address discrepancies
Prepare of the safety aggregated report for cross-functional review
Develop and maintain of the Medical Review Plan (MRP)
Provide expertise for study tool setup and maintenance (eCRF, eCRF Completion Guidelines, clinical database UAT, data analysis, and visualization systems)
Support in preparing materials for use in presentations and advisory committee meetings
Support training on medical aspects of the study to internal and external stakeholders
Serve as the first point of contact on medical issues of assigned studies
Ensure GCP compliance in the medical aspects of the study
Support protocol deviations cross-functional review, as appropriate
Review CIOMS reports and narratives in the clinical study report (CSR).
May work with the study team on study site feasibility.
May participate in expert working groups, project standard teams, and contribute to global process improvement efforts

Value Added

The Assoc. CSES assists to ensure the medical integrity of trial conduct in clinical studies/projects while collaborating effectively with the study team on study deliverables. The Assoc. CSES supports high-quality clinical trials and aims at drug approval.

Contribution Context

Individual Contributor X Team Member X Supervisor Manage Supervisors Team Leader Manage Function / Department

Work Interactions

Core Study Team
Global Clinical Lead / Clinical Development Lead/ Early Clinical Lead
Global Safety Lead
Data Monitoring Committee / Steering Committee/ Adjudication Committee
Country Lead Monitor / Clinical Research Associate

Qualifications

Minimum education and experience

MD, DO, PhD, PharmD, RN with a minimum of 1-2 years of industry experience in a pharmaceutical/biotech business and/or clinical experience

Preferred education and experience

MD degree is preferred;
Industry experience is not required but is a plus

Expertise, skills, and characteristics

Ability to acquire knowledge of different diseases and therapeutic areas
Proficient in GCP/ICH, FDA, EMA, and other relevant guidelines and regulations
Proactive, very flexible attitude
Adapts quickly to change
Able to work collaboratively across cultures and geographies
Strong communication skills

Organizational Relationship

Country Lead Monitor / Clinical Research Associate

YOUR APPLICATION

This is your opportunity to tackle the world’s biggest challenges with us: Maintaining our health, feeding growing populations and slowing the rate of climate change. You have a voice, ideas and perspectives and we want to hear them. Because our success begins with you. Be part of something big. Be Bayer.

Bayer welcomes applications from all individuals, regardless of race, national origin, gender, age, physical characteristics, social origin, disability, union membership, religion, family status, pregnancy, sexual orientation, gender identity, gender expression or any unlawful criterion under applicable law. We are committed to treating all applicants fairly and avoiding discrimination.

Location:

Spain : Cataluña : Barcelona

Division:

Pharmaceuticals

Reference Code:

868143

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Associate Clinical Study Excellence Scientist

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