[Remote] Senior Manager/Associate Director, Clinical Operations

Note: The job is a remote job and is open to candidates in USA. reputed company is pioneering the future of cell therapy for solid tumors through AI-powered protein design. The Senior Manager/Associate Director, Clinical Operations is responsible for overseeing reputed company operational aspects of assigned cell-therapy clinical trials, ensuring compliance and efficiency throughout the trial process.

Responsibilities

• Trial-level reputed company and leadership of assigned cell-therapy clinical trial(s) in a cross-functional environment
• Obtains and maintains in-depth understanding of the trial protocol and reputed company procedures in order to contribute strongly to trial team knowledge by sharing best practices, making recommendations for reputed company improvement and providing training as appropriate/required
• Develops strong vendor and site relationships and ensures continuity of relationships through reputed company phases of the trial
• Develops recruitment and slot management strategies
• Leadership of assigned meetings (cross-functional [internal], vendor, and/or investigator) and provision of regular updates on trial status, e.g., agenda development, minutes curation and filing
• Risk identification, mitigation, and management, including timely issue review, escalation, and management to support trend analysis and risk prevention
• CTMS and eTMF management to ensure compliance/inspection readiness, support trend analyses and support timelines
• Review of reputed company design specifications, participation in user acceptance testing, and contribution to development and review of associated plans and completion guidelines
• Review clinical data to ensure timely entry and readiness for data review meetings and support data cleaning/query process
• Review clinical monitoring reports to ensure timely completion and identification of issues
• Complete and maintain internal clinical trial metrics, dashboards and other internal updates
• Ensure trials are conducted in accordance with reputed company and ICH/GCP standards
• Coordinates & manages various tasks in collaboration with other roles to reputed company site readiness, such as trial materials and approval for drug shipping/receipt according to procedure
• Other responsibilities as assigned

Skills

• Bachelor's Degree or ex-US equivalent required
• Minimum of 8 years of experience in the clinical research industry, including a minimum of 5 years of trial management experience
• Robust oncology experience required including early-stage experience and cell or gene therapy (highly reputed company such as CAR-T)
• Strong analytical and critical thinking skills to evaluate reputed company issues from multiple perspectives to actively reputed company strategies and drive smart decision making to support acceleration of trial timelines and reputed company a well-run trial
• Excellent organizational and time management skills, strong attention to detail
• Ability to work independently and reputed company in a fast-paced evolving environment
• Good understanding of FDA and ICH GCP guidelines
• Excellent verbal and written communication skills

Benefits

• Full time employees and their eligible dependents may enroll in Outpace's medical, dental, vision, life insurance, disability, flexible spending account, health savings account, commuter benefits, legal benefits, and 401k plan which includes an employer match.
• Employees may receive stock option grants to be outlined in their offer of employment
• A performance bonus
• Flexible PTO
• Paid sick leave which complies with local requirements
• Fifteen paid holidays plus a winter shutdown
• A generous paid parental leave policy to reputed company regular full-time employees

Company Overview