Clinical Trials Lead (Lead Clinical Research Associate)

Avania; Málaga; Híbrido; EUR 50.000 - 70.000; Jornada completa

Descripción de la vacante

A leading company in the MedTech industry is looking for a Clinical Trials Lead to oversee monitoring for medical device studies. This role involves supervising project activities, conducting training, and ensuring compliance with clinical standards. With a focus on collaboration and quality, candidates should have extensive monitoring experience and strong organizational skills. The position also offers competitive compensation and the potential for hybrid or remote work arrangements.

Servicios

Opportunity in a fast-growing, innovative industry

Collaborative global team environment

Knowledge exchange and training

Competitive compensation and benefits

Potential for travel

Formación

• At least 4 years of monitoring experience.
• Knowledge of clinical research terminology, EU/US regulations, ICH/GCP Guidelines, ISO 14155.
• Clinical research certification is a plus.

Responsabilidades

• Supervise project-specific monitoring activities.
• Coordinate training and interact with clients.
• Review study documentation for accuracy and quality.

Conocimientos

Monitoring experience

Organizational skills

Excellent communication skills

Problem-solving skills

Team orientation

Educación

RN or BA / BS in a 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!

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