Sheridan Clinical Research, Inc. Work Values

Daily Duties at Sheridan Clinical Research, Inc.:

Manage all sites where clinical research is taking place (hospitals and private practices), all study coordinator report directly to Project Manager, schedule all pharma visits to research sites, set up all vendor contracts, financial manager of all budgets and contracts, review/revise Informed Consent Forms for proper language to match contracts and budgets, set up all project timelines, meet all EDC data entry timelines given by pharma, post metrics monthly to the company, train all new coordinators and enforce GCP/ICH training on new physicians and coordinators.

What they like about Sheridan Clinical Research, Inc.:

Working in an organization that is technologically advanced, creative, and innovative is critical in your assessment of hiring companies. Less important to you are stability of the organization, the length of time an organization has been in business, and the business' plans for the future. You prefer a fast-moving company that will take risks to achieve its goals and objectives. The length of time the company has been in business is irrelevant. Maintaining status quo is unnecessary. You thrive on change, uncertainty and the upside of potential business risks, especially those associated with innovation. Stability for the long haul is not nearly as important as is working in an atmosphere that is charged with a sense of urgency and constant change.

Tags

Project Manager, EDC, CTMS, Financial Reports, Data Entry, Clinical Research

Skills

Project Management, Timely Data Entry, Financial Reports, Billing Compliance, Hiring New Talent, Good Listener, Open Communicator, Contract Language, Prepare Consents, Metrics Charting, Labor Cost Analysis, Public Speaking, Medicare Billing, Meeting Scheduler and Organizer, Conduct Training Webinars, Supervising, Risk Management, Change Management

These are some of the questions we asked our climbers about their experiences with Sheridan Clinical Research, Inc.: