Especialista en Ensayos Clínicos Remotos

Agencia De Vivienda Y Rehabilitacion De Andalucia; Málaga; Remote; EUR 60,000 - 90,000; Full time

Benefits offered by this job

Remote work

Professional development opportunities

Job summary

Our client, a leading global pharmaceutical research organization, seeks a highly motivated Pharmacist to join their expanding clinical research division in a fully remote role. Ideally based in Granada or nearby, you will design, implement, and monitor trials with international teams.

You will ensure data integrity, master GCP and regulatory standards, and collaborate with investigators, sites, and regulators. Fluent in Spanish and English, you will manage study documents from home.

Qualifications

• Master's or Doctoral degree in Pharmacy or life sciences.
• At least 5 years in clinical research or related pharma field.
• Knowledge of GCP and regulatory affairs (FDA/EMA) and data capture systems.

Responsibilities

• Oversee and manage clinical trials ensuring GCP compliance and regulatory requirements.
• Collaborate with investigators and site staff for trial execution and patient safety.
• Review and interpret trial data, identify issues and propose solutions.
• Develop study protocols, informed consent forms, and essential documents.
• Manage drug accountability and storage/dispensing of investigational products.
• Act as a point of contact for study sites and queries.
• Participate in site selection, initiation, monitoring, and close-out visits (remote when possible).
• Contribute to analysis and reporting of trial results.
• Stay updated on developments in pharmaceutical research and regulatory affairs.

Skills

Analytical skills

Problem-solving

Organization

Bilingual communication

Regulatory knowledge

Remote work

Attention to detail

Education

Pharmacy degree

Tools

EDC systems

CTMS

Job description

Our client, a leading global pharmaceutical research organization, seeks a highly motivated Pharmacist to join their expanding clinical research division in a fully remote role. Ideally based in Granada or nearby, you will design, implement, and monitor trials with international teams.

You will ensure data integrity, master GCP and regulatory standards, and collaborate with investigators, sites, and regulators. Fluent in Spanish and English, you will manage study documents from home.