Clinical Trial Assistant

Planet Pharma; Milano; In loco; EUR 30.000 - 45.000; Tempo pieno

Descrizione del lavoro

A leading company in the pharmaceutical sector is seeking a Clinical Trial Associate (CTA) to support clinical trials. The role involves coordinating trial activities, ensuring compliance with regulatory standards, and managing documentation. Ideal candidates will have a background in life sciences or pharmacy, along with strong organizational and communication skills, and fluency in both English and Italian.

Competenze

• Bachelor's degree in life sciences, pharmacy, or related field.
• Previous experience in clinical research or trial coordination preferred.

Mansioni

• Assist in planning, coordination, and execution of clinical trials.
• Maintain and organize trial documentation, ensuring compliance with GCP.
• Support regulatory submissions and ethics committee approvals.

Conoscenze

Organizational Skills

Communication Skills

Knowledge of GCP

Knowledge of ICH Guidelines

Fluency in English

Fluency in Italian

Formazione

Bachelor's degree in life sciences

Bachelor's degree in pharmacy

Strumenti

Microsoft Office

Clinical Trial Management Systems

Descrizione del lavoro

Planet Pharma is seeking a Clinical Trial Associate (CTA) to support the execution of clinical trials in compliance with regulatory requirements and company standards. The CTA will play a crucial role in coordinating trial activities, ensuring documentation accuracy, and assisting with site management.

Key Responsibilities

• Assist in the planning, coordination, and execution of clinical trials.
• Maintain and organize trial documentation, ensuring compliance with Good Clinical Practice (GCP) guidelines.
• Support regulatory submissions and ethics committee approvals.
• Coordinate communication between study sites, investigators, and internal teams.
• Track study progress, ensuring timelines and milestones are met.
• Assist in budget management and vendor coordination.
• Prepare reports and presentations related to trial activities.

Qualifications & Skills

• Bachelor's degree in life sciences, pharmacy, or a related field.
• Previous experience in clinical research or trial coordination is preferred.
• Strong organizational and communication skills.
• Knowledge of GCP, ICH guidelines, and regulatory requirements.
• Proficiency in Microsoft Office and clinical trial management systems.
• Fluency in English and Italian is required.