20 publicaciones de empleo destacadas de clinical trial en spain (¡Están contratando!)

Clinical Trial Site Relationship Coordinator
Medpace, Inc. —Madrid, Madrid provincia
- Jornada completa
- Español
- Inglés
- Investigación
Assistant CRA
Thermo Fisher Scientific —En remoto
- Jornada completa
- Teletrabajo
- Servicio al cliente
- Inglés
- Microsoft Office
Clinical Research Associate I - Madrid
Fortrea —Madrid, Madrid provincia
- Jornada completa
- Servicio al cliente
- Inglés
- Investigación
Regulatory Operations Assistant - Clinical Trials
START Center for Cancer Research —Barcelona, Barcelona provincia
- De lunes a viernes
- Trabajo híbrido
- Inglés
- Gestión de equipo
- Habilidades de comunicación
Solicitud rápida
10d
Clinical Trial Coordinator
Thermo Fisher Scientific —En remoto
- Jornada completa
- Teletrabajo
- Microsoft Powerpoint
- Microsoft Word
- Microsoft Excel
Clinical Research Associate I - Barcelona
Fortrea —Barcelona, Barcelona provincia
- Jornada completa
- Servicio al cliente
- Inglés
- Investigación
Medical Science Liaison - Vaccines
CSL Seqirus —Barcelona, Barcelona provincia
- Jornada completa
- Español
- Doctorado
- Inglés
Study Support Assistant
ICON Plc —Barcelona, Barcelona provincia
- Jornada completa
- Microsoft Word
- Microsoft Excel
- Microsoft Outlook
- Seguro dental
- Seguro oftalmológico
Clinical Research Associate 2 - CFSP
IQVIA —Barcelona, Barcelona provincia
- Jornada completa
- Español
- Inglés
- Microsoft Office
- Teletrabajo opcional
Clinical Research Associate 2 - Multi-Sponsor - Based in Barcelona
IQVIA —Barcelona, Barcelona provincia
- Jornada completa
- Español
- Inglés
- Microsoft Office
- Teletrabajo opcional
Associate Clinical Programmer - Clinical Data Operations
Novartis —Barcelona, Barcelona provincia
- De 27.900 € a 51.900 € al año
- Jornada completa
- Informática
- Inglés
- Investigación
Medical Advisor Oncology
OncologyPipeline —Madrid, Madrid provincia
- Media jornada
Quality Assurance Specialist, Laboratory Services EU
CTI Clinical Trial Services, Inc —Bilbao, Vizcaya provincia
- Trabajo híbrido
- Microsoft Powerpoint
- Microsoft Word
- Microsoft Excel
- Teletrabajo opcional
Solicitud rápida
Clinical Research Associate
Opis s.r.l. —Madrid, Madrid provincia
- Hasta 48.000 € al año
- Jornada completa
- Inglés
- Microsoft Office
11d
Clinical Trial Assistant Senior
Sermes CRO —Madrid, Madrid provincia
- Inglés
Medical Writer (FSP) - Client Aligned
Thermo Fisher Scientific —En remoto
- Jornada completa
- Teletrabajo
- Grado
- Control de calidad
Clinical Biospecimen Scientist - Single Sponsor Dedicated
IQVIA —Madrid, Madrid provincia
- Jornada completa
- Grado
- Teletrabajo opcional
Regional Clinical Study Manager
BeiGene —En remoto
- De 71.400 € a 89.200 € al año
- Jornada completa
- Teletrabajo
- Microsoft Powerpoint
- Microsoft Word
- Microsoft Excel
Clinical Team Lead (CTL)
Evestia Clinical —Madrid, Madrid provincia
- Trabajo híbrido
- Servicio al cliente
- Inglés
- Investigación
Solicitud rápida
Associate Clinical Programmer - Clinical Study Data, Risk based Quality Management & Monitoring
Novartis —Barcelona, Barcelona provincia
- De 27.900 € a 51.900 € al año
- Jornada completa
- Informática
- SQL
- Grado

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Clinical Trial Site Relationship Coordinator

Medpace, Inc. -
Madrid, Madrid provincia

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Detalles del empleo

Jornada completa

Cualificaciones

Español
Investigación clínica
Inglés
Investigación
Microsoft Office
Máster
Grado
Habilidades de comunicación

Descripción completa del empleo

Job Summary :

Our clinical activities are growing rapidly, and we are currently seeking a full-time Clinical Trial Site Relationship Coordinator to join our vibrant Clinical Operations team in Spain, Madrid. This is a fantastic opportunity to work on pre-award and post-award study feasibilities, build and maintain strategic relationships with our network of sites, and develop key strategies to effectively conduct feasibilities in Spain. This position will fit someone who has previous clinical research experience or perhaps a CRA who would like to reduce travel.

If you want an exciting career within a company that excels in delivering innovative research and development of cutting edge drugs, where you can grow your potential, then this is the opportunity for you.

Responsibilities :

Provide ongoing support of sites, including identifying and discussing future new business opportunities and feasibility assessments;
Develop effective plans for site contact and follow-up;
Support management in expediting feasibility, site selection and study start-up; and
May be responsible for other projects and responsibilities as assigned.
Serve as site relations and excellence partner by providing oversight and building/retaining relationships of assigned sites within assigned country;
Conducting/expediting feasibility activities (standalone, blinded, initial, ongoing), supporting Management with site selection/alignment with studies and/or therapeutic areas, and study start-up;
Proactively research and understand specified site landscape/intelligence (KOL presence and knowledge, site capabilities, country standard of care and medical practices, etc.) as it relates to specific patient population, recruitment, and retention;
Building and maintaining relationships with preferred site networks/flagship sites which includes facilitating master CDAs and holding meetings with network directors
Conducting regular performance reviews for sites participating to our studies, ensuring quality study delivery
Serve as an escalation point for site related issues throughout the life cycle of a study
Provide ongoing support of sites, including identifying and discussing future new business;
Develop effective plans for site contacts, troubleshooting, and follow-up;
Develop an intelligence database with site and country intelligence
Support Management with process improvement initiatives regarding feasibility activities
Serve as main point of contact for project teams regarding site performance issues and updates on pertinent site information; and
May be responsible for other projects and responsibilities as assigned, including site Qualification Visits, prepping/consultation support for site audits, etc.

Qualifications :

Minimum a Bachelor of Science in health-related field;
Minimum 1 years' site and clinical trials experience (more experience for the more senior positions required);
CRA experience is an asset;
Knowledge of drug development, clinical trial management and operational procedures, including GCP guidelines preferred;
Knowledge of medical terminology and clinical patient management preferred;
Fluency in English; Spanish
Demonstrated organizational and prioritization skills;
Excellent oral and written communication skills; and
Proficient knowledge of Microsoft Office applications.

We kindly ask to send applications in English.

WHY MEDPACE?

At Medpace, you will find work that is both challenging and rewarding. At Medpace, you will be given the tools and training to succeed. At Medpace, you will be rewarded for strong performance and provided opportunities to grow professionally.

WHAT TO EXPECT NEXT

We look forward to receiving your application. A member of our recruitment team will review your qualifications. If interested, you will be contacted for an initial phone interview.

Medpace Overview :

Medpace is a full-service clinical contract research organization (CRO) providing phase l-lV clinical development services to the biotechnology, pharmaceutical, and medical device industries. Our mission is to accelerate the global development of safe and effective medical therapeutics through the advancement of clinical research. We leverage in-country regulatory and therapeutic expertise across all major therapeutic areas including oncology, cardiology, metabolic, endocrinology, central nervous system, and anti-viral and anti-infective. Headquartered in Cincinnati, Ohio, we employ more than 6,500 people across 40+ countries.

Why Medpace? :

When you join Medpace, you become part of an innovative team that brings cutting-edge therapies to market while building a meaningful and rewarding career focused on scientific excellence and improving patient outcomes around the world through continuous learning and cross-functional collaboration.

Purpose-Driven Work

- Work alongside physicians, scientists, and industry-leading experts committed to advancing the global development of medical therapeutics through clinical research excellence

Collaborative Culture

- Contribute to an interactive team environment that empowers decision making, creative thinking, and continuous learning through open communication and mutual trust.
- Leadership throughout Medpace is both accessible and approachable

Continuous Growth & Development

- Office based environment with on-site mentors
- Defined career paths with clear advancement opportunities
- Industry renowned onboarding and training programs designed to accelerate professional development
- Ongoing training and continuous learning opportunities throughout your career
- An environment that encourages employees to influence change, contribute ideas, and grow quickly

Other Employee Benefits

- Competitive compensation programs that recognize and reward performance
- Comprehensive health, wellness, retirement, and PTO benefits
- Office based culture with occasional WFH that provides flexibility for eligible positions after training
- Company-sponsored social events

Please note benefits may vary based on country.

What to Expect Next

A Medpace team member will review your application and if your profile matches our current needs, you will be contacted for an interview. While we review all applications carefully, we are unable to respond to every applicant, and only candidates selected for interviews will be contacted.

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clinical trial empleos en spain

Clinical Trial Site Relationship Coordinator

Assistant CRA

Clinical Research Associate I - Madrid

Regulatory Operations Assistant - Clinical Trials

Clinical Trial Coordinator

Clinical Research Associate I - Barcelona

Medical Science Liaison - Vaccines

Study Support Assistant

Clinical Research Associate 2 - CFSP

Clinical Research Associate 2 - Multi-Sponsor - Based in Barcelona

Associate Clinical Programmer - Clinical Data Operations

Medical Advisor Oncology

Quality Assurance Specialist, Laboratory Services EU

Clinical Research Associate

Clinical Trial Assistant Senior

Medical Writer (FSP) - Client Aligned

Clinical Biospecimen Scientist - Single Sponsor Dedicated

Regional Clinical Study Manager

Clinical Team Lead (CTL)

Associate Clinical Programmer - Clinical Study Data, Risk based Quality Management & Monitoring

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