Senior CRA – Oncology/Hematology (Lead, Global Trials)

WCT Clinical Research Spain, S.L.; Barcelona; Híbrido; EUR 60.000 - 90.000; Jornada completa

Descripción de la vacante

Worldwide Clinical Trials is hiring a Senior Clinical Research Associate to protect patient safety, ensure data quality, and oversee monitoring across Spain. This home-based role travels approximately 8–10 days per month to investigative sites and coordinates with sponsors and global study teams.

The candidate should have 3+ years of CRA experience with an MD or Pharmacy qualification or equivalent life sciences degree, and a strong knowledge of ICH/GCP and regulatory requirements.

Formación

• Education and CRA experience: an MD or Pharmacy qualification with at least 3 years' CRA experience; or a min four-year degree with at least 5 years' CRA experience; or nursing/life sciences with at least 7 years' CRA experience.
• Extensive knowledge of clinical research principles, FDA/EU regulations, ICH Guidelines, and SOPs.
• Strong therapeutic-area expertise to operate as Lead CRA where appropriate.

Responsabilidades

• Lead site qualification, initiation, interim monitoring, management, and close-out activities.
• Protect patient safety and data integrity via source data verification and CRF reviews.
• Coordinate CRAs as Lead CRA on global studies and provide mentoring and training.

Conocimientos

Communication skills

Organizational skills

Problem solving

Team leadership

Educación

MD or Pharmacy qualification (MSPH, PharmD, PhD, equivalent)

Nursing or life sciences degree

Herramientas

Microsoft Office

IxRS

EDC systems

Descripción del empleo

Worldwide Clinical Trials is hiring a Senior Clinical Research Associate to protect patient safety, ensure data quality, and oversee monitoring across Spain. This home-based role travels approximately 8–10 days per month to investigative sites and coordinates with sponsors and global study teams.

The candidate should have 3+ years of CRA experience with an MD or Pharmacy qualification or equivalent life sciences degree, and a strong knowledge of ICH/GCP and regulatory requirements.