Senior Clinical Research Associate - Remote

Overview

The Senior Clinical Research Associate is responsible for ensuring compliance and performance for assigned clinical research protocols and sites, contributing to the advancement of healthcare solutions.

In Short

• Accountable for performance and compliance of clinical research studies.
• Acts as primary site contact and manager throughout trial phases.
• Develops and maintains strong relationships with clinical sites.
• Conducts various site visits and monitors compliance with regulations.
• Communicates effectively with investigators and site staff.
• Identifies and resolves site performance issues.
• Mentors junior CRAs and supports training initiatives.
• Participates in audit and inspection activities.
• Works in collaboration with internal and external stakeholders.
• Contributes to continuous improvement of CRA processes.

Requirements

• Associate’s or Bachelor’s degree in a scientific/healthcare discipline.
• At least 7 years of relevant experience in healthcare, with 4 years in site management.
• Fluency in local language and English, with strong communication skills.
• Excellent understanding of clinical research and GCP/ICH guidelines.
• Proven skills in site management and patient recruitment.
• Strong IT skills and ability to adapt to new technology.
• Experience in conducting motivational site visits.
• Ability to analyze data and implement corrective actions.
• Effective time management and organizational skills.
• Capable of working independently and in a multicultural environment.

Benefits

• Opportunity to work in a leading biopharmaceutical company.
• Engagement in meaningful work that impacts patient health.
• Support for professional development and continuous learning.
• Flexible working arrangements including remote work.
• Inclusive and diverse workplace culture.