Junior R&D Chef – Innovación En Alimentos

Hospitality Connection Barcelona Sl

Madrid

Presencial

EUR 55.000 - 75.000

Jornada completa

hace 47 horas
Sé de los primeros/as/es en solicitar esta vacante
Generador de candidaturas

Transforma esta oferta en una entrevista — un currículum y una carta de presentación creados pensando en lo que quiere el empleador.

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Ventajas ofrecidas por este puesto de trabajo

Health insurance
Annual leave entitlements
Retirement planning
LifeWorks/EAP programme
Life assurance
Flexible benefits

Descripción de la vacante

ICON Strategic Solutions in Madrid is seeking a Senior Clinical Research Associate to oversee multicenter trial activities, ensure protocol adherence, and maintain data integrity across sites.

You will travel extensively (60%+) to monitor sites, collaborate with cross-functional teams, and provide site staff training, with a focus on regulatory compliance and patient safety throughout the study lifecycle.

Formación

  • Advanced degree in life sciences, nursing or medicine.
  • Extensive experience as a CRA with knowledge of trial processes and regulatory requirements.
  • Proven ability to manage multiple sites and projects.
  • Excellent communication and stakeholder management skills.
  • Ability to travel at least 60% with a valid driver''s license.

Responsabilidades

  • Monitoring clinical trial sites to ensure adherence to study protocols, regulatory requirements, and GCP standards.
  • Conducting site visits to assess site performance, resolve issues, and provide support for successful trial execution.
  • Collaborating with cross-functional teams to ensure timely and accurate data collection and reporting.
  • Providing training and guidance to site staff and other CRAs to maintain high standards of clinical trial conduct.
  • Building and maintaining effective relationships with site personnel and stakeholders to facilitate smooth trial operations.

Conocimientos

Monitoring practices
Data integrity
Site management
Regulatory requirements
GCP standards
Communication skills
Travel readiness

Educación

Advanced degree in life sciences, nursing, or medicine

Herramientas

Clinical trial software

Descripción del empleo

Sr. Clinical Research Associate

At ICON Strategic Solutions, you will work in a sponsor-dedicated model, supported by ICON's global expertise. As the world's largest FSP organisation, with over 90 sponsor partnerships, we offer stability, career development and a collaborative environment where your work contributes to the development of treatments that benefit patients worldwide. We are currently seeking a Senior Clinical Research Associate (CRA) to join our diverse and dynamic team. As a Senior CRA at ICON Plc, you will play a critical role in overseeing and managing clinical trial activities to ensure they are conducted according to protocol, regulatory requirements, and industry standards. You will contribute to the success of clinical trials by ensuring data integrity, participant safety, and compliance throughout the study lifecycle.

What You Will Be Doing:
  • Monitoring clinical trial sites to ensure adherence to study protocols, regulatory requirements, and Good Clinical Practice (GCP) standards.
  • Conducting site visits to assess site performance, resolve issues, and provide support to ensure successful trial execution.
  • Collaborating with cross-functional teams to ensure timely and accurate data collection and reporting.
  • Providing training and guidance to site staff and other CRAs to maintain high standards of clinical trial conduct.
  • Building and maintaining effective relationships with site personnel and stakeholders to facilitate smooth trial operations.
Your Profile:
  • Advanced degree in a relevant field such as life sciences, nursing, or medicine.
  • Extensive experience as a Clinical Research Associate, with a strong understanding of clinical trial processes and regulatory requirements.
  • Proven ability to manage multiple sites and projects simultaneously, with strong organizational and problem-solving skills.
  • Expertise in monitoring practices, data integrity, and site management, with proficiency in relevant clinical trial software and tools.
  • Excellent communication, interpersonal, and stakeholder management skills, with the ability to influence and drive compliance within a complex environment.
  • Ability to travel at least 60% of the time (international and domestic - fly and drive) and should possess a valid driver's license.
What ICON can offer you:
  • Competitive salary.
  • Various annual leave entitlements.
  • A range of health insurance offerings to suit you and your family's needs.
  • Competitive retirement planning offerings to maximize savings and plan with confidence for the years ahead.
  • Global Employee Assistance Programme, LifeWorks, offering 24-hour access to a global network of over 80,000 independent specialized professionals who are there to support you and your family's well-being.
  • Life assurance.
  • Flexible country-specific optional benefits, including childcare vouchers, bike purchase schemes, discounted gym memberships, subsidized travel passes, health assessments, among others.

We are committed to providing a workplace free of discrimination and harassment. All qualified applicants will receive equal consideration for employment without regard to race, color, religion, sex, sexual orientation, gender identity, national origin, disability or protected veteran status. If, because of a medical condition or disability, you need a reasonable accommodation for any part of the application process, or in order to perform the essential functions of a position, please let us know or submit a request here.

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