Junior Clinical Trial Protocol Writer – Oncology Research

MEDSIR; Barcelona; Híbrido; EUR 18.000 - 24.000; Jornada completa

Ventajas ofrecidas por este puesto de trabajo

Hybrid working model

Study compensation for transport and食

MacBook provided (Apple)

Courses & workshops access

Conferences participation

Birthday day off

Diversity & inclusion

Descripción de la vacante

MEDSIR, a Barcelona-based biotechnology company, offers an opportunity for a trainee to contribute to the design and revision of clinical trial proposals and protocols in oncology. You will assist in scientific and medical writing, collaborate with experts, and support registry setup to advance trials worldwide.

As a trainee, you will develop skills in medical writing, project planning, and regulatory compliance while benefiting from a hybrid work model and opportunities to participate in

Formación

• University degree in health or life science-related field.
• Basic understanding of clinical research principles; GCP training valued.
• Solid writing and organizational skills with attention to detail.

Responsabilidades

• Assist in generating and reviewing scientific documents for trial design.
• Identify scientific/clinical assumptions impacting project plan and budget.
• Ensure deliverables comply with ICH, GxPs and guidelines.
• Set up new clinical trials in registries (clinicaltrials.gov, EUCT).
• Monitor deadlines and ensure timely delivery of projects.
• Stay updated with medical literature and trends.
• Support defense of proposals with external clients and collaborators.
• Participate in department procedures and administrative tasks.
• Protect information and report security concerns as required.
• Adhere to Ethics & Compliance and attend trainings.

Conocimientos

English proficiency

Writing skills

Team collaboration

Analytical thinking

Educación

Health or life sciences degree

Herramientas

MS Office

Clinical trial registries

Descripción del empleo

MEDSIR, a Barcelona-based biotechnology company, offers an opportunity for a trainee to contribute to the design and revision of clinical trial proposals and protocols in oncology. You will assist in scientific and medical writing, collaborate with experts, and support registry setup to advance trials worldwide.

As a trainee, you will develop skills in medical writing, project planning, and regulatory compliance while benefiting from a hybrid work model and opportunities to participate in