Clinical Research Specialist - Remote

Overview

The Clinical Research Specialist is responsible for ensuring compliance and performance for assigned clinical research protocols and sites. This role acts as the primary contact for sites throughout the study phases and works to develop new research sites.

In Short

• Accountable for site compliance and performance in clinical trials.
• Acts as primary site contact and manager.
• Develops strong relationships with clinical sites.
• Performs monitoring activities in compliance with regulations.
• Coordinates tasks to achieve Site Ready status.
• Conducts various types of site visits and documentation.
• Communicates effectively with investigators and site staff.
• Identifies and resolves site performance issues.
• Supports audit and inspection activities.
• Contributes to the identification of new potential clinical research sites.

Requirements

• Experience in clinical research and site management.
• Knowledge of ICH/GCP and local regulations.
• Strong communication and interpersonal skills.
• Ability to manage multiple tasks and priorities.
• Proficiency in clinical data management systems.
• Experience with regulatory documentation processes.
• Strong problem-solving skills.
• Adaptability to changing environments.
• Ability to work independently and as part of a team.
• Familiarity with clinical trial monitoring tools.

Benefits

• Opportunity to work in a leading global healthcare company.
• Engagement in meaningful clinical research projects.
• Professional development opportunities.
• Collaboration with a diverse team of experts.
• Flexible working arrangements.
• Contribution to advancements in global healthcare.