20 publicaciones de empleo destacadas de clinical research en la moraleja, md (¡Están contratando!)

Senior Clinical Research Associate - MedTech
IQVIA —Madrid, Madrid provincia
- Jornada completa
- Microsoft Powerpoint
- Microsoft Word
- Microsoft Excel
Nutriasesor Hospital y Residencias - Málaga
IQVIA —Madrid, Madrid provincia
- Jornada completa
- Trabajo híbrido
- Hospital
- Habilidades de comunicación
- Formación continua
- Ayuda al desarrollo profesional
Senior Clinical Project Manager (Renal, Obesity, MASH) - Global Study Leadership
IQVIA —Madrid, Madrid provincia
- Jornada completa
- Investigación
- Project management
- Grado
- Teletrabajo opcional
7d
Global Regulatory Scientist
ICON Plc —Madrid, Madrid provincia
- Jornada completa
- Grado
- Seguro dental
- Seguro oftalmológico
Medical Strategy Lead, Oncology-Clinical Development (Centre of Excellence)
IQVIA —Madrid, Madrid provincia
- Horas extra
- Inglés
- Investigación
- Desarrollo de negocios
- Teletrabajo opcional
Associate Principal - Global Custom Integrated Research
IQVIA —Madrid, Madrid provincia
- Jornada completa
- Trabajo híbrido
- Inglés
- Investigación
- Desarrollo de negocios
Regulatory & Quality Lead – AI IVD Diagnostics
SpotLab —Madrid, Madrid provincia
- Jornada completa
- Trabajo híbrido
- Español
- Inglés
- Bachillerato
Solicitud rápida
Senior Medical Writer - Early Phase (Single Sponsor Support)
Syneos - Clinical and Corporate - Prod —Madrid, Madrid provincia
- Jornada completa
- Inglés
- Investigación
Senior Clinical Trial Manager - Internal Medicine
ICON Plc —Madrid, Madrid provincia
- Jornada completa
- Inglés
- Grado
- Liderazgo
- Seguro dental
- Seguro oftalmológico
Associate Medical Director- Neurology
IQVIA —Madrid, Madrid provincia
- Jornada completa
- Inglés
- Desarrollo de negocios
- Teletrabajo opcional
Delegado Derma y Estética - Madrid
IQVIA —Madrid, Madrid provincia
- 30.000 € al año
- Jornada completa
- Habilidades de comunicación
- Enfermería
Associate Director, Field Medical Execution - Neuroscience
Novartis —Madrid, Madrid provincia
- De 73.100 € a 135.700 € al año
- Jornada completa
- CRM software
- Doctorado
- Inglés
Associate Pharmacovigilance Project Manager (Europe)
PrimeVigilance —Madrid, Madrid provincia
- Jornada completa
- Teletrabajo
- Project management
- Liderazgo
Solicitud rápida
CRA I-II in Madrid. Sponsor dedicated.
サイネオス・ヘルス —Madrid, Madrid provincia
- Grado
9d
Senior Director, Drug Development
IQVIA —Madrid, Madrid provincia
- Jornada completa
- Microsoft Powerpoint
- Microsoft Excel
- Investigación
- Teletrabajo opcional
Associate Medical Director, Cardiology , with Metabolic Diseases and Nephrology Experience
IQVIA —Madrid, Madrid provincia
- Jornada completa
- Inglés
- Desarrollo de negocios
- Teletrabajo opcional
Medical Safety Director, Clinical Scientist
IQVIA —Madrid, Madrid provincia
- Jornada completa
- Doctorado
- Teletrabajo opcional
1d
Senior Site Contract Associate - IQVIA Biotech
IQVIA —Madrid, Madrid provincia
- Jornada completa
- Investigación
- Microsoft Office
- Grado
- Teletrabajo opcional
Senior Statistician
PSI CRO —Madrid, Madrid provincia
- Jornada completa
- Inglés
- Máster
Solicitud rápida
8d
Compliance - Senior Consultant (Life Science exp mandatory)
IQVIA —Madrid, Madrid provincia
- Jornada completa
- Trabajo híbrido
- Inglés
- Máster
- Grado

Quiero recibir la alerta de empleo más reciente de clinical research en la moraleja, md

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Senior Clinical Research Associate - MedTech

IQVIA -
Madrid, Madrid provincia

Solicitar ahora

Detalles del empleo

Jornada completa

Cualificaciones

Microsoft Powerpoint
Microsoft Word
Microsoft Excel
Investigación clínica
Inglés
Investigación
Grado

Descripción completa del empleo

Madrid, Spain | Full time | Field-based | R1551724

Job Overview
Perform monitoring and site management work to ensure that sites are conducting the study(ies) and reporting study data as required by the study protocol, applicable regulations and guidelines, and sponsor requirements.

Essential Functions

Perform site monitoring visits (selection, initiation, monitoring and close-out visits) in accordance with contracted scope of work and Good Clinical Practice.
Work with sites to adapt, drive, and track subject recruitment plan in line with project needs to enhance predictability.
Administer protocol and related study training to assigned sites and establish regular lines of communication with sites to manage ongoing project expectations and issues.
Evaluate the quality and integrity of study site practices related to the proper conduct of the protocol and adherence to applicable regulations. Escalate quality issues as appropriate.
Manage the progress of assigned studies by tracking regulatory submissions and approvals, recruitment and enrollment, case report form (CRF) completion and submission, and data query generation and resolution. May support start-up phase.
Ensure copies/originals (as required) site documents are available for filing in the Trial Master File (TMF) and verify that the Investigator's Site File (ISF) is maintained in accordance with GCP and local regulatory requirements.
Create and maintain appropriate documentation regarding site management, monitoring visit findings and action plans by submitting regular visit reports, generating follow-up letters and other required study documentation.
Collaborate and liaise with study team members for project execution support as appropriate.
If applicable, may be accountable for supporting development of project subject recruitment plan on a per site basis.
If applicable, may be accountable for site financial management according to executed clinical trial agreement and retrieve invoices according to local requirement.

Qualifications

Bachelor's Degree Scientific discipline or health care preferred. Req
Requires at least 2 years of on-site monitoring experience. Req
Equivalent combination of education, training and experience may be accepted in lieu of degree. Req
Good knowledge of, and skill in applying, applicable clinical research regulatory requirements.
i.e., Good Clinical Practice (GCP) and International Conference on Harmonization (ICH) guidelines.
Good therapeutic and protocol knowledge as provided in company training.
Computer skills including proficiency in use of Microsoft Word, Excel and PowerPoint and use of a laptop computer and iPhone and iPad (where applicable).
Written and verbal communication skills including good command of English language.
Organizational and problem-solving skills.
Effective time and financial management skills.
Ability to establish and maintain effective working relationships with coworkers, managers, and clients.

IQVIA is a leading global provider of clinical research services, commercial insights, and healthcare intelligence to the life sciences and healthcare industries. We create intelligent connections to accelerate the development and commercialization of innovative medical treatments to help improve patient outcomes and population health worldwide. Learn more at https://jobs.iqvia.com.

IQVIA is committed to integrity in our hiring process and maintains a zero tolerance policy for candidate fraud. All information and credentials submitted in your application must be truthful and complete. Any false statements, misrepresentations, or material omissions during the recruitment process will result in immediate disqualification of your application, or termination of employment if discovered later, in accordance with applicable law. We appreciate your honesty and professionalism.

At IQVIA, we believe that diversity, inclusion, and belonging empower our mission to accelerate innovation for a healthier world. We create a culture of belonging by valuing the perspectives of all talented employees worldwide and providing them with the opportunity to power smarter healthcare for everyone, everywhere. When our talented employees bring their authentic selves and their diverse experiences to work, they enable us to accomplish extraordinary things. Multifaceted thought processes spark innovation. Multi-talented collaboration harnesses innovation to deliver superior outcomes. Likewise, as part of this culture, IQVIA is committed to ensuring effective equality between women and men, integrating it as a strategic principle in its corporate and human resources policies.

Where you'll work

Field-based

You’ll work where the action is — out in the field, directly engaging with our customers, sites or partners. Field-based roles offer the opportunity to build relationships face-to-face, gain real-world insights and make a tangible impact.

Culture

Culture at IQVIA is built on a shared belief: that when people are empowered with better data, smarter technology and deeper expertise, they can change what’s possible for patients. Across every team and every corner of the globe, you’ll find colleagues who genuinely care — about the mission and about each other. That’s what makes this a place where people tend to stay, grow and do the best work of their careers.

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clinical research empleos en la moraleja, md

Senior Clinical Research Associate - MedTech

Nutriasesor Hospital y Residencias - Málaga

Senior Clinical Project Manager (Renal, Obesity, MASH) - Global Study Leadership

Global Regulatory Scientist

Medical Strategy Lead, Oncology-Clinical Development (Centre of Excellence)

Associate Principal - Global Custom Integrated Research

Regulatory & Quality Lead – AI IVD Diagnostics

Senior Medical Writer - Early Phase (Single Sponsor Support)

Senior Clinical Trial Manager - Internal Medicine

Associate Medical Director- Neurology

Delegado Derma y Estética - Madrid

Associate Director, Field Medical Execution - Neuroscience

Associate Pharmacovigilance Project Manager (Europe)

CRA I-II in Madrid. Sponsor dedicated.

Senior Director, Drug Development

Associate Medical Director, Cardiology , with Metabolic Diseases and Nephrology Experience

Medical Safety Director, Clinical Scientist

Senior Site Contract Associate - IQVIA Biotech

Senior Statistician

Compliance - Senior Consultant (Life Science exp mandatory)

Quiero recibir la alerta de empleo más reciente de clinical research en la moraleja, md

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