Wcct Global Work Values

Daily Duties at Wcct Global:

• Studies included Phase I trials covering topics of, but not limited to: endocrinology, respiratory, and ophthalmology. • Other studies included Phase II-III trials covering topics of, but not limited to: infectious disease, gastrointestinal disease, and respiratory. • Established and tracked clinical study milestones/timelines for the site(s); provided feedback to all parties as milestones/timelines change. • Effectively communicated relevant project information to WCCT Global management and peers. Performed in-house monitoring for studies under my purview before sponsor monitoring visits. • Served as liaison between WCCT Global clinical team, WCCT Global business development team, WCCT Global management, Sponsor, Vendor(s), and monitor(s); passed along communications, updates, and escalated issues to all members involved for resolution in a timely fashion. • Reviewed study contracts/budgets and provided relevant budgetary limits to the appropriate departments; approved vendor/ site invoices based on contract allowances. As needed, provided budget accrual projections to WCCT Global management. • Communicated to Sponsor to effectively identify needs and emerging issues. • Managed day-to-day operational aspects of a clinical trial, and provided oversight and guidance to the WCCT Global clinical team consisting of approximately 20 individuals. • Provided performance feedback to team members regarding study conduct achievements and/or failures. • Consistently acknowledged and appreciated each team member's contributions. • Assisted in keeping track of lessons learned and share those lessons with team members. • Excellent competency with EDC. • As a member of their full service CRO, performed site initiation visits, monitoring visits and managed master trial files for all sites. • Collaborated with Billing and Accounts Payable to ensure sponsors are billed based upon completion of study initiatives.

What they like about Wcct Global:

Organizations with strong, centralized leadership are particularly attractive to you. You require a work environment with leadership that aggressively seeks to expand and grow the business and does so in a visible and decisive manner. In general you prefer to work in an environment in which there is a strong link between leadership, its actions, and a strong set of company-wide values.

Tags

Irvine, CCRP, regulatory affairs, clinical project manager, EDC, budgets , timelines, contracts and budgets

Skills

clinical research regulatory procedure, clinical project manager, supervisor multiple employees, Maintained Trial Master File as in-house CRA, Protocol Writing, Negotiate budgets and contracts for clinical trials

These are some of the questions we asked our climbers about their experiences with Wcct Global: