Source Document Specialist - Remote

Overview

The Source Document Specialist at Care Access is responsible for creating, maintaining, and controlling accurate versions of source documents for clinical trials, contributing to the mission of revolutionizing access to clinical trials for patients.

In Short

• Full-time remote position.
• Create and maintain source documents for clinical trials.
• Ensure compliance with GCP Guidelines and 21 CFR Part 11.
• Design accurate e-Source documents based on clinical trial protocols.
• Review and update source documents as needed.
• Maintain version control of all documents.
• Communicate with site staff and internal departments.
• Minimal travel requirements.
• Work independently while prioritizing tasks.
• Good verbal and written communication skills required.

Requirements

• Experience as a Clinical Research Coordinator preferred.
• Skilled in e-Source build and design.
• Proficient in creating and revising paper source templates.
• Ability to interpret clinical trial protocols.
• Self-motivated and detail-oriented.
• Proficient in Excel and other IT skills.
• Organizational skills are essential.
• Bachelor's degree in a relevant field or equivalent experience.

Benefits

• PTO/vacation days, sick days, holidays.
• 100% paid medical, dental, and vision insurance.
• 75% coverage for dependents.
• HSA plan.
• Short-term and long-term disability insurance.
• 401k retirement plan.
• Culture of growth and equality.