A company is looking for a Remote Contract Analyst (Informed Consent Specialist).
Key Responsibilities
Act as the primary contact for clinical studies regarding informed consent (IC) activities
Coordinate the timely and compliant completion of the IC approval process
Develop and maintain strong relationships with research centers and internal teams
Required Qualifications
Bachelor's degree in Clinical Research, Biology, or Chemistry
Minimum of 2 years of experience in informed consent / contracts within clinical research
Experience in document management and compliance with standard operating procedures
Ability to work collaboratively with diverse teams
Familiarity with clinical trial agreements and regulatory standards
Specialist Remote • Humble, Texas, United States