Senior Director, Clinical Field Monitoring and Trial Operations

Remote – US based candidates only, no visa sponsorship available.

Responsibilities

• Own and enhance the clinical monitoring strategy, with a focus on risk-based and fit-for-purpose models
• Establish monitoring standards, templates, and best practices to improve operational efficiency
• Design and implement a contract field monitoring team, alongside sourcing, staffing, and onboarding
• Oversee complete monitoring processes from site qualification to trial close-out, ensuring compliance with quality standards
• Identify and manage site-level risks and data quality issues through root cause analysis

Qualifications

• Bachelor's degree with 14+ years of clinical monitoring experience in the biotech/pharma industry or an equivalent combination of education and experience
• Proven track record in developing and managing Clinical Monitoring Teams, SOPs, and related infrastructure
• Familiarity with Trial Master File (TMF) quality control processes
• Willingness to travel up to 30% for meetings and monitoring activities

Pay

$260,965 – $309,341 annually

Benefits

• Comprehensive health benefits and wellness programs
• Opportunities for professional growth and development
• Flexible work arrangements to promote work-life balance