[Remote] Clinical Trial Manager (Contract)

Note:The job is a remote job and is open to candidates in USA. Allogene Therapeutics is a clinical-stage biotechnology company focused on developing allogeneic CAR T cell products for cancer and autoimmune diseases. The Clinical Trial Manager will oversee clinical trials, ensuring compliance, data quality, and effective communication across teams, while managing study deliverables and operational issues. Responsibilities• Manage all clinical aspects of study under oversight of Clinical Operations senior management including initial operational feasibility, study timelines, budget and metrics; study document development and review (training documentation, ICF, study specific plans, eCRF Guidelines, lab and radiology manuals, etc.), plans and manages study-specific meetings (e.g., Study Team Meetings, Investigator meetings, etc.).• Interface with cross-functional teams as Clinical Operations regional or global study lead (e.g., Medical Monitor, Regulatory Affairs, CMC/Supply Chain, CRO, vendors and Investigators/site staff). Work cross-functionally and with external vendors to proactively manage the execution of the clinical trial. • May oversee clinical trial execution in one or more regions within a global clinical trial. • Review protocol and amendment development, Informed Consent Forms, clinical trial-related training, and Site Study Tools• Ensure clinical trial execution in compliance with the protocol and ICH/GCP guidelines/regulations, including the review of monitoring reports, protocol deviations, and eTMF• Partner with Clinical Quality Assurance to follow through on corrective and preventative actions (CAPA) identified during internal and external audits• Vendor oversight: effectively communicate expectations to CRO, ensure appropriate site management, hold CRO accountable to timelines, and verify quality metrics• Provide study-specific training and leadership to clinical research staff, including CRO, CRAs, sites and other contract personnel.• Manage study budget; review and approve clinical invoices against approved scope of work and budget, evaluate and approve vendor change orders, coordinating review of updates or revisions with key cross-functional partners, as necessary. • Prepare and present project debriefings to Clinical Operations management. • Provide study-related guidance and leadership to internal and external partners, as appropriate. Skills• Bachelor's degree or equivalent combination of education/experience in science or health-related field with at least 3 years of clinical trial management experience in a Pharmaceutical/Biotech organization.• Clinical trial management experience as a contractor or employee of an industry sponsor• Vendor management• Robust understanding of ICH/GCP, and knowledge of regulatory requirements. • Strong clinical study/project management skills. • Excellent communication and organizational skills (ability to prioritize a number of tasks of varying complexity), along with problem solving, conflict resolution, leadership and team-building skills. • Candidates must be authorized to work in the U.S. • Prior clinical trial experience in oncology therapeutic development with an industry sponsor or Contract Research Organization• Multi-regional study management experience advantageousCompany Overview• Allogene Therapeutics is a biotechnology company catalyzing cancer treatment through the development of CAR T therapy.It was founded in 2017, and is headquartered in South San Francisco, California, USA, with a workforce of 201-500 employees. Its website is Apply tot his job