Clinical Trial Associate

Key Responsibilities:

• Perform administrative tasks for clinical trial execution, including document development and information reconciliation.
• Track study status updates weekly and manage study-specific information using databases and spreadsheets.
• Review and approve study documentation, such as essential document packets and informed consent forms.

Operational Support:

• Manage clinical and non-clinical supplies, including purchase and shipping processes.
• Assist with site binder development and coordinate meetings with minute-taking and distribution.
• Support protocol training for vendors and sites, and coordinate laboratory sample movement and data tracking.

Qualifications and Environment:

• Requires a Bachelor's degree (scientific discipline preferred) and at least 1 year of related experience, with openness to entry-level candidates.
• Must have proficiency in Microsoft Office and other applications, with strong organizational and communication skills.
• Role is primarily remote with periodic on-site meetings, requiring ability to work in a fast-paced, confidential environment.