Clinical Trial Manager/Senior Clinical Trial Manager

1 month ago

San Francisco, California, United States Nurix Therapeutics Full time

Nurix is seeking a Clinical Trial Manager (CTM)/Sr. CTM to join the Clinical Operations team. This individual will be responsible for management of global regions and/or clinical programs. They will lead study team, vendors, clinical monitors and clinical sites throughout the life cycle of a clinical trial.

This individual will be able to manage clinical regions or trial(s) and have broad involvement in work central to Nurix's strategic goals. They will apply existing technical skills, learn new skills, and play a key role in clinical development of the programs. As an early hire, they'll be influential in championing and developing Nurix's culture.

The CTM/Sr. CTM is responsible for the successful implementation of a clinical trial, independently, from start-up to close-out. Experience in managing cross-functional teams, vendor oversight, knowledge of applicable regulatory requirements and developing junior staff will be essential to the team's success. The CTM/Sr. CTM will represent Clinical Operations at Project team meetings and may represent Nurix at professional events.

Job Responsibilities:

Accountable for all operational aspects of assigned clinical trial(s) or geographical region.Responsible for selection of vendors/CROs and provide effective ongoing management and oversight to vendors/CROs to ensure compliance and execution of deliverables within the approved budget, study timeline, and study protocolWorks closely with investigative site personnel, CROs, and other study vendorsMonitor and track clinical trial progress and provide status update to stakeholdersManage study contracting, budget, forecasting, accruals and payment process for all clinical trial vendors including investigational sitesCollaborate with Data Management to ensure correct CRFs content is collected, prepare/implement CRF completion guidelines, and coordinate delivery of data updates, listings and study reportsDrafts and coordinates review of relevant documents including protocols, informed consents, case report forms, monitoring plans, investigator brochures and clinical study reports.Must be able to participate in cross-functional strategic initiatives under limited supervisionProactively identifies potential issues/risks and recommends/implements solutionsProvides leadership to the clinical operations team working on the assigned program
Experience and SkillsB.S./ B.A. in biological sciences, advanced degree preferred with 5-10 years of relevant industry experienceAbility to travel as required for the program (10-15%)Demonstrated knowledge of FDA, ICH and GCP regulations and guidelinesExperience in leading teams, including CROs, consultants and vendorsMust display strong analytical and problem-solving skills at a project level and collaborate with colleagues to generate solutionsStrong communication and influence skills and ability to create a clear sense of directionAbility to deal with time demands, incomplete information or unexpected eventsOutstanding organizational skills with the ability to work independently, multi-task and prioritizeComfortable in a fast-paced small company environment and able to adjust workload based upon changing priorities Nurix Therapeutics, Inc. is committed to protecting and respecting your privacy and personal information, including information collected by Nurix when you apply for a job with Nurix or in the course of your employment with Nurix. By applying for a position at Nurix, you agree to our collection and use of personal information as described in our Privacy Policy ( ).

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