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

Clinical Budget Specialist - FSP Team
Fortrea —Madrid, Madrid provincia
- Jornada completa
- Trabajo híbrido
- Investigación
- Microsoft Office
- Máster
Clinical Research Associate - French Speaking - Any EMEA location
North American Science Associates Ltd. —San Sebastián de los Reyes, Madrid provincia
- Jornada completa
- Inglés
- Investigación
- Máster
Solicitud rápida
2d
Medical Affairs Business Analyst - Pharma R&D
Roche —Madrid, Madrid provincia
- Jornada completa
- DevOps
Medical Science Liaison
サイネオス・ヘルス —Madrid, Madrid provincia
- Doctorado
- Investigación
- Liderazgo
1d
Software Engineer for Healthcare Sector Projects
GMV —Tres Cantos, Madrid provincia
- Trabajo híbrido
- Seguro dental
13d
Clinical Trial Manager - Oncology
ICON Plc —Madrid, Madrid provincia
- Jornada completa
- Grado
- Seguro dental
- Seguro oftalmológico
Sr. Clinical Project Manager (Europe)
Allucent —Madrid, Madrid provincia
- Trabajo híbrido
- Microsoft Powerpoint
- Microsoft Word
- Microsoft Excel
- Programa de recomendación
Solicitud rápida
Associate Principal / Principal, Clinical Outcome Assessment (COA) Strategy Consulting
IQVIA —Madrid, Madrid provincia
- Jornada completa
- Trabajo híbrido
- Doctorado
- Investigación
- Máster
Medical Science Liaison
Syneos Health Commercial Solutions —Madrid, Madrid provincia
- Doctorado
- Investigación
- Liderazgo
13h
Medical Scientist Lead
Gilead Sciences —Madrid, Madrid provincia
- Jornada completa
- Español
- Doctorado
- Inglés
Medical Strategy Lead, Oncology-Clinical Development (Centre of Excellence)
IQVIA —Madrid, Madrid provincia
- Horas extra
- Inglés
- Investigación
- Desarrollo de negocios
- Teletrabajo opcional
Medical Engagement Partner Cardiometabolic Diseases - Andalucia, Extremadura, Murcia y Canarias
Roche —Madrid, Madrid provincia
- Jornada completa
- Inglés
- Investigación
- Máster
Associate Director - Clinical Project Management (IQVIA Biotech)
IQVIA —Madrid, Madrid provincia
- Jornada completa
- Microsoft Powerpoint
- Microsoft Word
- Microsoft Excel
- Teletrabajo opcional
7d
Associate/ Study Start Up Manager, IQVIA Biotech
IQVIA —Madrid, Madrid provincia
- Jornada completa
- Grado
- Liderazgo
- Habilidades de comunicación
- Teletrabajo opcional
Global Regulatory Scientist
ICON Plc —Madrid, Madrid provincia
- Jornada completa
- Grado
- Seguro dental
- Seguro oftalmológico
Principal Biostatistician
Ergomed —Madrid, Madrid provincia
- Jornada completa
- Teletrabajo
- Inglés
- Investigación
- Microsoft Office
Solicitud rápida
Clinical Sales Representative - ADD - Madrid
Abbott Laboratories —Madrid, Madrid provincia
- Jornada completa
- Doctorado
- Hospital
- Investigación
Medical Engagement Partner Cardiometabolic Diseases - Noreste y Norte
Roche —Madrid, Madrid provincia
- Jornada completa
- Inglés
- Investigación
- Máster
Senior Medical Writer - Early Phase (Single Sponsor Support)
Syneos - Clinical and Corporate - Prod —Madrid, Madrid provincia
- Jornada completa
- Inglés
- Investigación
14d
Clinical Operations Manager
ICON Plc —Madrid, Madrid provincia
- Jornada completa
- Project management
- Grado
- Liderazgo
- Seguro dental
- Seguro oftalmológico
8h

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

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Clinical Budget Specialist - FSP Team

Fortrea -
Madrid, Madrid provincia

Solicitar ahora

Detalles del empleo

Jornada completa

Cualificaciones

Investigación clínica
Derecho
Investigación
Microsoft Office
Máster
Grado
Negociación

Descripción completa del empleo

Join Our Team and Shape the Future of Clinical Research!

At Fortrea , we are dedicated to streamlining clinical trials and ensuring compliance with global regulations. As a Site Budget & Contract Specialist , you will play a critical role in negotiating and managing site agreements, confidentiality agreements, and other key contracts that support our clinical research efforts. Your work will help drive the success of groundbreaking studies while ensuring compliance and efficiency.

In this role, you will be part of our FSPx team and work directly with one of our renowned key sponsor to advance the development of innovative, life-changing medications.

Key Responsibilities:

In this role, you will:

Support Country Study site budget template, parameter, and payment term building to ensure timely setup of individual site budgets.
Manage and execute assigned study site budget maintenance activities through life of study.
Negotiate directly with globally assigned sites master clinical trial agreements rate cards.
Partner with site payment department to ensure site budget and payment terms compatibility with payment systems and EDC requirements.
Partner with internal Study Startup team, Clinical Operations teams, and TAU partners to improve overall SB&C metrics and implement processes.
Ensure standards are applied to the SB&C processes across projects, portfolios and support continuous improvement activities while developing TA-aligned strategies.
Leverage leading industry tools and data sources to provide budget and payment terms feedback aligned with parameters and fair market value guidance.
Promptly recognize and improve potential delays and escalate non-performance.

Required Qualifications:

To succeed in this role, you should have:

Bachelor’s degree (LLB, JD, BA, or BS) preferred ; a university-level law degree is highly desirable (UK/EU).
Fortrea may consider equivalent relevant experience in lieu of educational requirements.
2–4 years of experience in contract negotiation, clinical research, or a related field.
Demonstrated global experience in both budget planning and budget negotiations , including independently developing study budets and benchmarking them against fair market value standards.
Experience working with grant management systems and grant planning tools , supporting accurate financial planning and tracking.
Familiarity with U.S. CPT codes for medical procedures is highly valued.
Strong understanding of ICH GCP guidelines and clinical research processes.
Excellent negotiation, communication, and organizational skills .
Ability to work independently and manage multiple priorities in a fast-paced environment.
Proficiency in Microsoft Office and contract tracking systems.
Ability to work independently and manage multiple priorities in a fast-paced environment.

What We Offer:

Competitive salary and performance-based incentives.
Flexible work arrangements (remote/hybrid options).
Professional growth opportunities in a collaborative and innovative environment.
The opportunity to work on cutting-edge clinical research projects.

Ready to Make an Impact?

Take the next step in your career and join us in driving innovation in clinical research.

Apply today! Applications are reviewed on a rolling basis—don’t miss this opportunity!

Learn more about our EEO & Accommodations request here .

Solicitar ahora

Refina tu búsqueda

clinical research empleos en tres cantos, md

Clinical Budget Specialist - FSP Team

Clinical Research Associate - French Speaking - Any EMEA location

Medical Affairs Business Analyst - Pharma R&D

Medical Science Liaison

Software Engineer for Healthcare Sector Projects

Clinical Trial Manager - Oncology

Sr. Clinical Project Manager (Europe)

Associate Principal / Principal, Clinical Outcome Assessment (COA) Strategy Consulting

Medical Science Liaison

Medical Scientist Lead

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

Medical Engagement Partner Cardiometabolic Diseases - Andalucia, Extremadura, Murcia y Canarias

Associate Director - Clinical Project Management (IQVIA Biotech)

Associate/ Study Start Up Manager, IQVIA Biotech

Global Regulatory Scientist

Principal Biostatistician

Clinical Sales Representative - ADD - Madrid

Medical Engagement Partner Cardiometabolic Diseases - Noreste y Norte

Senior Medical Writer - Early Phase (Single Sponsor Support)

Clinical Operations Manager

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

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