Clinical Safety Scientist - Remote

Overview

The Clinical Safety Scientist is responsible for supporting safety reporting in clinical trials across various therapeutic areas as part of investigational product development programs.

In Short

• Support safety reporting activities for multiple clinical trials.
• Review, manage, and create individual case safety reports.
• Generate safety queries to ensure case report accuracy.
• Prioritize daily work for timely submission into the safety database.
• Collaborate with cross-functional colleagues as needed.
• Basic understanding of scientific and medical concepts.
• Strong communication skills in English.
• Advanced computer and database skills.
• Ability to identify and escalate problems.
• Time management and organizational skills.

Requirements

• M.D. with minimum 1 year of clinical work experience or 2 years in drug safety.
• Experience in a patient care setting preferred.
• Knowledge of GCP and ICH regulations.
• Ability to work as part of a cross-functional team.
• Strong organizational skills.
• Excellent oral and written communication skills.
• Advanced computer skills.

Benefits

• Flexible work arrangements.
• Opportunity to work in a global healthcare leader.
• Engagement in innovative healthcare solutions.
• Ethical integrity and support for career development.