The Clinical Research Center, Inc, Work Values

Daily Duties at The Clinical Research Center, Inc, :

• Assist in the identification of potential study sites • 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 • Monitor trials throughout their duration by conducting various Site Monitoring visits (including PSVs, SIVs, IMVs and COVs) to meet study expectations for different types of trials • Review CRF’s, data management plans, study reports, and informed contents • Conduct source data/document Verification (SDV) • 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 (AE/SAE) 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

What they like about The Clinical Research Center, Inc, :

You highly value a work environment built on a formal structure, rules, and regulations. You do not enjoy the unpredictability of shifting priorities and deadlines that upset your routine. You require and enjoy direction, input and accountability as part of your work environment. You have a strong need to participate in making key decisions and feel left out if your superiors or co-workers do not seek your input when making decisions. You thrive on providing good customer service to both internal or external customers, and doing so makes you feel good.

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, :