Senior Clinical Research Associate – Global Oncology Trials

optimapharm-doo; Madrid; Presencial; EUR 45.000 - 60.000; Jornada completa

Ventajas ofrecidas por este puesto de trabajo

Performance bonus

Referral bonus

Flexible work hours

Work from home allowance

Health insurance

Training and development program

Well-being programs

Employee engagement programs

Descripción de la vacante

Optimapharm is seeking an experienced CRA to join our global clinical research team. Based in Spain (Madrid or Barcelona), you will monitor sites, ensure patient safety, data integrity, and compliance with GCP/ICH guidelines across oncology, neurology, and infectious disease studies.

You will work independently within a matrix environment, collaborate with investigators, manage site visits, perform CRF review, and contribute to trial budgets and site contracts while advancing your career in a

Formación

• University degree in medicine, pharmacy, dentistry, or equivalent
• Fluent in local language and English (written and spoken)
• Knowledge of GCP/ICH guidelines and regulatory requirements
• Ability to read, analyze, and interpret scientific/technical journals
• Excellent verbal and written communication skills
• Current, valid driver's license

Responsabilidades

• Perform routine site visits independently across the region
• Manage assigned sites with regular contact to ensure enrolment and compliance
• Independently perform CRF review and resolve queries
• Identify risks and retraining opportunities for site personnel
• Prepare CAPA plans for issues identified during monitoring and follow up until resolution
• Prepare EC submission documents and translations, and perform other tasks as instructed
• Negotiate study budgets with investigators and assist with site contracts
• Support administration of site payments per project instructions

Conocimientos

Clinical research

GCP/ICH knowledge

English fluency

Regulatory understanding

Computer proficiency

Educación

University degree in medicine/pharmacy/dentistry or equivalent

Descripción del empleo

Optimapharm is seeking an experienced CRA to join our global clinical research team. Based in Spain (Madrid or Barcelona), you will monitor sites, ensure patient safety, data integrity, and compliance with GCP/ICH guidelines across oncology, neurology, and infectious disease studies.

You will work independently within a matrix environment, collaborate with investigators, manage site visits, perform CRF review, and contribute to trial budgets and site contracts while advancing your career in a