Associate Clinical Trial Manager

Job Responsibilities

• Drive the operational planning, content, execution, and delivery for one or more clinical trials.
• Act as the main point of contact for assigned CRO and translational vendors to ensure GCP compliance and adherence to the scope of work while maintaining budgets and timelines. Responsible for trial related activities from startup to close-out of a clinical trial in close collaboration with internal stakeholders and CROs.
• Support trial deliverables both in clinical and translational in a proactive and quality manner
• Contribute to the development and implementation of study related documents such as protocol amendments, plans, and tracking tools.
• Foster effective communication and collaboration with internal and external stakeholders, such as investigators, study sites contract research organizations (CROs), and vendors
• Participate in process improvement and quality-related initiatives associated with study execution and deliverables; participate in establishment of best-in-class processes and standards for study conduct
• Contribute to a collaborative culture within and outside Clinical Development and actively manage best practice sharing and capability building within the clinical team

Qualifications And Education Requirements

• Bachelor's degree with minimum 3+ years of industry experience
• Phase I oncology experience
• Excellent project management skills, particularly, with managing CROs, consultants, and vendors in a team environment
• Excellent interpersonal skills