CRA Trainee

MEDSIR; Barcelona; Híbrido; EUR 30.000 - 38.000; Jornada completa

Ventajas ofrecidas por este puesto de trabajo

Transport & meal support

Work with clinicians

Fast growth

Hybrid working model

GoodHabitz courses

Conferences & events

Work-from-abroad policy

Young international team

Birthday day off

Company events

Diversity & equal opportunity

Modern workplace near Sagrada Familia

MacBook provided

Descripción de la vacante

MEDSIR, a Barcelona-based biotechnology company focused on oncology clinical trials, invites applications for a CRA Trainee. You will provide technical, logistics and administrative support to projects while embracing our collaborative, fast-growing culture.

This role requires a university degree in a related field; a Master’s in Clinical Trials Monitoring is highly valued. You will work in a small team, maintain trial documents, generate reports, and attend training and investigator meetings.

Formación

• Signed agreement with your academic centre is mandatory.
• University degree in a related field.
• Master’s degree in Clinical Trials Monitoring.
• Strong interpersonal, communication, facilitation and presentation skills.
• Strong analytical and problem-solving skills.
• Demonstrated ability to work in a small team setting.
• Good computer skills, proficient with MS Office applications.
• Ability to communicate effectively in both official languages is an asset.
• Excellent organizational skills with demonstrated ability to execute support on projects on time and on budget.

Responsabilidades

• Collaborate with project coordination as required.
• Update and generate as-built documents; assist with field change requests to resolve design issues.
• Understand and perform document control functions in accordance with on-site policy and procedures.
• Guarantee traceability of all clinical trial documents.
• Maintenance of clinical trial files, either in digital or paper.
• Support on monitoring activities contracted.
• Support on study supplies management, control and logistic activities.
• Support and control administrative tasks (monitors...).
• Support to generate reports, graphs and presentations of clinical trials.
• Attendance to investigators, CRAs and training meetings whenever possible.

Conocimientos

Interpersonal skills

Communication skills

Analytical skills

Problem-solving

Teamwork

MS Office proficiency

Bilingual in official languages

Educación

Bachelor's degree in related field

Master’s degree in Clinical Trials Monitoring

Herramientas

MS Office

Descripción del empleo

WHY CHOOSE MEDSIR

We are a Barcelona-based fastest-growing company founded by scientific experts. We are dedicated to the design and management of innovative strategic clinical trials in oncology, from study conception to the publication of study results. Together, we create the best strategies that are both clinically relevant and scientifically meaningful. We strive to improve our knowledge of this complex disease and the vast array of available treatments in a fast-innovative way.

At MEDSIR, you will have the job of your life while working together towards our shared mission bringing novel treatments to cancer patients worldwide. We welcome top performers that will bring new ideas, diverse perspectives, and provide you the opportunities and freedom to grow and make a real impact in patients' lives and science… all while having great fun

ABOUT THE OPPORTUNITY:

IMPORTANT REQUIREMENT

1. Signed agreement with your academic centre MANDATORY

As a CRA TRAINEE you will provide technical, logistics and administrative support to the different projects assigned.

HOW YOU WILL CONTRIBUTE:

• Collaborate with project coordination as required.
• Participate in the continuous updating and accurate generation of as-built documents, assisting with the research and preparation of field change requests to resolve design issues.
• Understand and perform document control functions in accordance with on-site policy and procedures.
• Guarantee traceability of all clinical trial documents.
• Maintenance of clinical trial files, either in digital or paper.
• Support on monitoring activities contracted.
• Support on study supplies management, control and logistic activities.
• Support and control administrative tasks (monitors...).
• Support to generate reports, graphs and presentations of clinical trials.
• Attendance to investigators, CRAs and training meetings whenever possible.

WHAT DO WE VALUE FOR THIS OPPORTUNITY?

• A university degree in a related field.
• A Master’s degree in Clinical Trials Monitoring.
• A university degree in a related field.
• Strong interpersonal, communication, facilitation and presentation skills.
• Strong analytical and problem-solving skills.
• Demonstrated ability to work in a small team setting.
• Good computer skills, proficient with MS office applications.
• Ability to communicate effectively in both official languages is an asset.
• Excellent organizational skills with demonstrated ability to execute support on projects on time and on budget.

THE THINGS YOU REALLY WANNA KNOW:

At MEDSIR, we believe that employees today want to evolve in collaborative, high-growth environments where they can demonstrate their abilities and thrive both professionally and personally. We are convinced that employees need to find alignment between their inner values and their company’s culture and mission to unlock their full potential. We work to create a culture of empowerment, continuous learning and growth where everyone can bring expertise, own projects and easily measure their impact.

BENEFITS

• Study compensation support for basic transport and food expenses
• Work with world-renowned clinicians and KOL´s on high-level publications and papers.
• Fast growth, we are an early-stage company with a multidisciplinary team and many growth opportunities.
• Work-life balance - hybrid working model and flexible hours focusing on performance rather than office hours.
• Unlimited access to GoodHabitz courses and regular workshops (external & internal) to continue your development.
• Opportunities to participate in scientific conferences & events at national and international level.
• Work-from-abroad policy depending on position and local legislation.
• A young & international team with a company culture focused on development.
• Positive, dynamic, and passionate work environment.
• A free day on your birthday so you can truly celebrate!
• Unforgettable MEDSIR events and regular get togethers.
• Equal employment opportunity, at MEDSIR we proudly pursue a diverse workforce and celebrate our differences.
• A fantastic workplace located near Sagrada Familia.
• We work with MacBook computer (Apple).

If you believe you match our values, you are unique and feel ready to make a change, we look forward to meeting you!

We are committed to fostering a diverse and inclusive workplace, where all individuals are treated with respect and equality, regardless of race, gender, age, religion, disability, or any other characteristic. We believe in providing equal opportunities for all and do not tolerate discrimination in any form.