Senior Global Trial Associate

Contributes to the operational execution of clinical studies, provides operational input on development and management of study deliverables, and supports Global Trial Lead in ensuring eTMF accuracy and completion.

Requirements

• Knowledge of ICH/GCP, regulatory guidelines and directives, and the drug development process
• Working knowledge of project management
• Effective oral/written communication and presentation skills
• Ability to collaborate with key stakeholders and across the organization
• Mentors and coaches other team members and GTA's, as appropriate
• Develops and maintains collaborative relationships with internal and external stakeholders

Benefits

• Competitive benefits
• Services and programs to provide work-life balance
• Opportunities for career growth and development