The Clinical Research Center, Inc Work Values

Daily Duties at The Clinical Research Center, Inc:

• Identify/ select investigators who will be responsible for the conduct of the trial • Set up the trial sites, which includes ensuring each center has the trial materials, including the investigational medicinal product • Review CRF's, data management plans, study reports, and informed consents • Conduct source data/document verification (SDV) • Monitor trials throughout their duration by conducting various Site Monitoring visits (Including PSVs, SIVs, IMVs, ad COVs) to meet study expectations for different types of trials • Perform training of the site staff to trial-specific industry standards • Perform drug accountability ensuring that sites receive and maintain study drug according to the protocol • Report adverse events according to regulations and company policy • Write visit reports and close out trial sites on completion of the trial • Liaise with doctors/ consultants or investigators on conducting the trial • Verify that data entered on the CRFs is consistent with patient clinical notes • Collect completed CRFs from hospitals and general practices • Training the site staff to trial – specific industry standards

What they like about The Clinical Research Center, 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

CRA II, PSVs, SIVs, IMVs, COVs, GCP, FDA REGULATIONS, EDC, AE/SAE REPORTING

Skills

Proficient in prioritizing and completing tasks in a timely manner, Flexible with excellent multitasking skills, Highly detailed –oriented, with superior record retention and time management skills, Excellent communication, interpersonal and organizational skills, Ready and willing to accommodate frequent local, domestic or international business travels, Microsoft Office applications – Microsoft Word, Microsoft Office Excel, PowerPoint

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