Study Start Up Specialist - Remote

Overview

This role involves supporting project management and regulatory activities during site start-up, acting as the main contact for study personnel.

In Short

• Support project management and regulatory activities.
• Act as the main contact for study personnel at sites.
• Prepare and distribute start-up documents.
• Track site start-up activities using designated systems.
• Provide reports on study start-up metrics.
• Establish relationships with site personnel.
• Follow-up on start-up documents with sites.
• Plan site start-up activities.
• Ensure compliance with regulatory requirements.
• Coordinate with legal teams as necessary.

Requirements

• Experience in project management.
• Knowledge of regulatory processes.
• Strong communication skills.
• Ability to track and report on project metrics.
• Experience with contract management.
• Detail-oriented and organized.
• Ability to establish relationships with stakeholders.
• Proficient in using project management tools.
• Experience in clinical research is a plus.
• Ability to work independently and as part of a team.

Benefits

• Competitive salary.
• Opportunities for professional development.
• Supportive work environment.
• Health and wellness programs.
• Flexible working hours.
• Access to training resources.
• Collaborative team culture.
• Potential for career advancement.
• Work-life balance initiatives.
• Comprehensive benefits package.