TMF Specialist: Study File & Compliance

TFS HealthScience; Madrid; Presencial; EUR 35.000 - 50.000; Jornada completa

Descripción de la vacante

A global Contract Research Organization is seeking a Trial Master File Associate to manage the TMF and support the study team. The ideal candidate has at least 2 years of experience in the CRO or pharmaceutical industry with knowledge of GCP/ICH guidelines. Strong communication, organizational skills, and a Bachelor's degree in Health Science are preferred. This role offers competitive compensation and the chance for professional growth in a collaborative environment.

Servicios

Competitive compensation package

Comprehensive benefits

Opportunities for personal and professional growth

Formación

• At least 2 years of experience in CRO or Pharmaceutical Industry with proven TMF Management.
• Advance level of English.
• Knowledge of GCP/ICH guidelines.

Responsabilidades

• Organize, maintain, and oversee the Trial Master File (TMF).
• Provide TMF Monthly Reports.
• Act as contact person for study team.

Conocimientos

TMF Management

Communication Skills

Organizational Skills

Teamwork Ability

Document Management Software

Educación

Bachelor’s Degree in Health Science or Document Management

Herramientas

VEEVA

Descripción del empleo

A global Contract Research Organization is seeking a Trial Master File Associate to manage the TMF and support the study team. The ideal candidate has at least 2 years of experience in the CRO or pharmaceutical industry with knowledge of GCP/ICH guidelines. Strong communication, organizational skills, and a Bachelor's degree in Health Science are preferred. This role offers competitive compensation and the chance for professional growth in a collaborative environment.