¡Activa las notificaciones laborales por email!

Clinical Trials Lead (Lead Clinical Research Associate)

Avania

Albacete

Híbrido

EUR 45.000 - 70.000

Jornada completa

Hace 4 días
Sé de los primeros/as/es en solicitar esta vacante

Mejora tus posibilidades de llegar a la entrevista

Elabora un currículum adaptado a la vacante para tener más posibilidades de triunfar.

Descripción de la vacante

A leading company in the MedTech industry is seeking a Clinical Trials Lead. You will oversee clinical trial monitoring activities, ensuring the highest standards while coordinating training and client interaction. The role offers exciting challenges and opportunities for growth in a collaborative and innovative environment, with options for hybrid and remote work.

Servicios

Opportunity in a fast-growing industry
Collaborative global team
Knowledge exchange and training
Competitive compensation and benefits
Potential for travel
Hybrid and remote work options

Formación

  • At least 4 years of monitoring experience in clinical trials.
  • Experience mentoring and training new CRAs.
  • Clinical research certification is a plus.

Responsabilidades

  • Supervise project-specific monitoring activities and coordinate training.
  • Interact with clients as the primary contact for study questions.
  • Review study documentation for accuracy and quality.

Conocimientos

Organizational skills
Time management
Problem-solving skills
Excellent communication
Professional writing skills
Strong relationship-building
Team orientation
Clinical research knowledge

Educación

RN or BA / BS in science, engineering, or health-related field

Herramientas

Excel

Descripción del empleo

Avania is hiring - Clinical Trials Lead (Lead Clinical Research Associate!)

As a Clinical Trials Lead (Lead Clinical Research Associate), you will work with a sponsoring company in monitoring medical device and MedTech studies, ensuring the highest ethical and clinical standards.

You will supervise project-specific monitoring activities, coordinate training, interact with clients, and act as the primary contact for study questions. You will organize team training, generate monitoring tools, and ensure visits are conducted properly and tasks completed timely. You will also review study documentation for accuracy and quality, and represent Avania in conference calls and meetings.

The Lead CRA collaborates with the Project Manager to meet study objectives and may handle CRA activities as needed. You will support CRAs, assist with challenging situations, conduct co-visits, review reports, and perform similar tasks.

This position requires travel of approximately 25-30%.

We seek candidates with :

  • RN or BA / BS in a science, engineering, or health-related field plus at least 4 years of monitoring experience
  • Knowledge of clinical research terminology, EU / US regulations, ICH / GCP Guidelines, ISO 14155, and ability to learn across therapeutic areas
  • Experience mentoring and training new CRAs
  • Ability to conduct monitoring visits and complete documentation
  • Organizational, time management, and problem-solving skills
  • Excellent communication and professional writing skills
  • Computer proficiency, especially in Excel
  • Experience creating training presentations and coordinating training
  • Strong relationship-building skills and team orientation
  • Ability to generate monitoring tools and deliver presentations
  • Ability to address questions and escalate issues to sponsors
  • Clinical research certification is a plus

We offer :

  • Opportunity to work in a fast-growing, innovative industry
  • Collaborative global team environment
  • Knowledge exchange, training, and career development
  • Competitive compensation and benefits
  • Potential for travel
  • Hybrid and remote work options available

We look forward to receiving your application!

LI-DNI

J-18808-Ljbffr

Consigue la evaluación confidencial y gratuita de tu currículum.
o arrastra un archivo en formato PDF, DOC, DOCX, ODT o PAGES de hasta 5 MB.