Clinical Trials CRA Trainee — Hybrid, Growth & Impact

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

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.