Urgent requirement for one of our top clients located in “SSF,CA”.
Please contact me at your earliest convenience, along with job No. CTM_51408 to xxxxxx.xxxxxx@xxxxxxxxx.xxx
Description:
The Clinical Trial Manager II is accountable for the day-to-day operations of 1-4 clinical trials commensurate with complexity, including trial start-up, conduct, and close-out activities. Leads the Protocol Execution Team (PET) to ensure that trial timelines, costs, and quality metrics are met. Ensures accuracy and timeliness of vendor and site payments. Oversees forecasting of clinical/non-clinical supplies. Establishes study milestones and ensures accurate tracking and reporting of study metrics. Manages trial-specific collaborations with other research entities (e.g., Cooperative Group Trials, Investigator Sponsored Trials, Global Partner Trials). Performs ongoing vendor management (e.g., CROs, IVRS, Reading Centers), including independent negotiation of scope of work, budgets, performance management, and issue resolution . Creates and manages clinical trial budgets and staffing/resourcing plans.
Requirement:
Bachelor.s Degree with a minimum of five years of clinical research experience Therapeutic knowledge preferred. Knowledge of GCP and ICH . Proficient computer skills . Travel may be required. Extensive clinical research knowledge and cross-functional understanding of clinical trial methodology.
Contact:
The most effective way of communication is via email please forward us your updated WORD FORMAT resume (Address, Contact number and email is must) to *** xxxxxx.xxxxxx@xxxxxxxxx.xxx ***
Please mention your best hourly rate, availability and visa status. Any questions, do feel free to email us.
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