Senior Clinical Research Associate

Role Overview:

• This role contributes to clinical research by managing monitoring activities across Phase I–IV trials and Real World Evidence studies.
• It ensures study quality, regulatory compliance, and site performance throughout the clinical development lifecycle.

Key Responsibilities:

• Oversee clinical site management, conduct monitoring visits, and maintain investigator relationships.
• Support study start-up, regulatory documentation, and patient enrollment strategies.
• Collaborate with data management and project teams to ensure data quality and compliance.

Qualifications:

• Minimum of 1 year clinical trial monitoring experience with a bachelor's degree in healthcare or life sciences.
• Strong knowledge of ICH-GCP guidelines, regulatory requirements, and clinical trial systems.
• Excellent organizational and communication skills, with ability to work independently.

Benefits:

• Competitive compensation with sign-on bonus up to $10,000 and fully remote work.
• Comprehensive health benefits, vacation packages, and paid parental leave.
• Structured mentoring, leadership development, tuition reimbursement, and training resources.