Medicus Research is looking for a monitor with the following requirements and skills:

Basic Duties:

 Locate and assess suitable study centers
 Set-up study centers — ensure that each center has the trial materials and check that the investigator and the site staff know exactly what has to be done
 Monitor clinical trials throughout its duration which will involve visiting the study centers on a regular basis to check the patient data in the case report forms (CRFs)
 Validate and collect completed CRFs from sites
 Verify that data entered on to the CRFs is consistent with patient clinical notes, known as source data/document verification (SDV)
 Sort out any problems which may arise
 Prepare required study documentations and visit report
 Ensure all unused trial supplies are accounted for
 Close down study centers on completion of the trial
 Discuss results with the investigator and CRO representatives
 Archive study documentation and correspondence
 Prepare final reports and occasionally manuscripts for publication

Requirements and Skills:

• Applicant should have a Bachelor Degree in Science and have a grade point average over 3.0
• Knowledge of basic clinical system and procedures
• Should have at least five (5) years experience as a Clinical Research Associate
• Excellent organizational skills
• Result oriented and ability to successfully manage multi-tasking environment
• Excellent verbal and written communication skills
• Persuasive and with high level of people handling skills
• Proficient in Microsoft Office Professional, Outlook, and Web based system

Interested applicants may send their comprehensive resume with application letter and salary history to lucy.msryan@staywellresearch.com

• Location: Northridge, CA
• Compensation: DOE
• Principals only. Recruiters, please don’t contact this job poster.
• Please, no phone calls about this job!
• Please do not contact job poster about other services, products or commercial interests.