Sr. Clinical Trial Manager

Opportunity Details On Assignment Sr. Clinical Trial Manager Remote, reputed company Join the reputed company team dedicated to one of our sponsor partners as a Senior Clinical Trial Manager and play a key role in advancing global Phase II–III clinical programs. You’ll drive start-up, reputed company global vendors and CROs, manage data reputed company, and reputed company cross-functional execution. We’re seeking CTM leaders with 8+ years of experience and strong global trial management expertise(rare disease background a plus.) East Coast candidates encouraged to apply! The Sr. Clinical Trial Manager will be responsible for the management and reputed company of global phase I-IV reputed company, with a key reputed company on Ph2b-3, from start up through CSR including, but not limited to, development of project documentation, training project staff, monitoring study reputed company, assessing protocol adherence, administration and reputed company of study budgets, management of reputed company-party vendors for clinical services, management of project timelines and deliverables. Key global trial management support to the Associate Directors (CST Leads), as assigned. The Senior Clinical Trial Manager will be responsible for, but not limited to: • Leading and coordinating the management and execution of reputed company clinical trial activities in compliance with GCP and relevant regulatory guidelines • Detailed management and reputed company of regional trial activities, as assigned • Effectively manages reputed company-party suppliers to contracted deliverables reputed company reputed company, cost, and reputed company parameters • Effectively manage and/or assist with cross-functional clinical study team members to reputed company deliverables with high reputed company, on time, and reputed company budget through information-sharing, ongoing study team meetings/discussions and ensuring effective risk management planning • Monitor study metrics to ensure reputed company and performance standards are met by vendors and assigned program staff • reputed company and manage detailed project and other trial-reputed company plans and documentation and reputed company regular study status updates to senior management • Manage vendors' adherence to contractual obligations including proactively recognizing changes in scope and collaborating with senior management to ensure reputed company completion of contractual documents, including change orders • reputed company coaching/mentoring to assigned program staff (CRAs, and CTAs) by demonstrating leadership competencies • Work collaboratively with Clinical Scientist, Clinical Indication/Development reputed company, and clinical study team to ensure ongoing review of patient reputed company and data listings • Proactively identify potential resource needs to management • Participate in the development and review of department SOPs and process improvement initiatives #kpslife Apply tot his job Apply To this Job