Clinical Sciences Associate Director – Early Development, Oncology

Location: Remote - US based candidates only, no visa sponsorship available

Responsibilities

• Support early phase clinical trials focusing on data quality and integrity
• Author clinical protocols and regulatory documents ensuring clarity and consistency
• Implement data management plans and oversee data review processes
• Analyze and present trial data for internal decision-making and regulatory submissions
• Manage collaborations and projects with external consultants and CROs
• Proactively identify and resolve issues across cross-functional teams
• Collaborate on the development of clinical study documents and training resources

Qualifications

• Doctorate degree with 3 years of clinical development experience, or equivalent alternative qualifications
• Experience in a pharmaceutical industry setting, particularly in oncology or similar therapeutic areas
• Proven track record in clinical trial process improvements within a study team environment
• Strong communication skills for conveying complex scientific concepts to stakeholders
• Familiarity with regulatory compliance and Good Clinical Practice standards for trial implementation
• Proficiency in data analysis tools such as Spotfire for clinical data insights
• Experience contributing to regulatory submissions and scientific publications

Benefits

• Comprehensive employee benefits including medical, dental, and vision coverage
• Generous company contributions to retirement and savings plans
• Discretionary annual bonus program and stock-based long-term incentives
• Award-winning time-off plans promoting work/life balance
• Flexible work models to accommodate different working arrangements

Pay

$169,793 – $229,720 annually