CRA REGIONAL HOME BASED CLINICAL RESEARCH ASSOCIATE

FULL TIME SALARIED Regional Monitors 6 months-20 years experience needed for top global CRO.

Have you done 6+ months of clinical site monitoring outside (not to be confused with in-house monitoring) on your own-site initiation, close-out, etc??? You are the candidate we seek!

 

PLEASE APPLY ONLY IF YOU HAVE SOME INDEPENDENT SITE MONITORING EXPERIENCE IN THE FIELD, RATHER THAN IN-HOUSE.  PLEASE SEND RESUME TO dave@davehands.com WITH A SHORT NOTE EXPLAINING THE DETAILS OF YOUR OUTSIDE CLINICAL MONITORING EXPERIENCE AT THE SITES.

 

Salary $60,000-$82,000. Home office expense reimbursement available. Must be close to an airport.

 

The worlds most successful CRO is growing it's staff of regional home based clinical research associates (CRA's).  Their unbelievable growth has caused them to add staff which means more regionalized travel for it's monitors than they have known in the past!  One goal is to regionalize the travel so that CRA's are not flying coast to coast by increasing staff.  Travel still expected to be about 65%, but regionalized.

 

 

They have more depth of therapeutic expertise and a broader range of services than any other service provider. They conduct both US and Global trials in all therapeutic areas. In fact, this CRO conducts more clinical trials than anyone else in the world. Become involved in work that improves the quality of life for people around the globe. Let your career soar! We are seeking an enthusiastic CRA to join the team. The clinical research associate monitors activities at clinical study sites to assure adherence to Good Clinical Practices (GCPs), SOPs, and study protocols. Review regulatory documents as required and prepare site visit reports. Responsible for multiple projects and must work both independently and in a team environment. May participate in the study development and start-up process including reviewing protocols, designing and/or reviewing CRFs, preparing Informed Consent forms, developing study documents, organizing and presenting at investigator meetings, working with management on monitoring strategy, and/or developing project-specific CRA training. Participate in clinical training programs and maintain awareness of developments in the field of clinical research. Position will be filled at CRA or Sr CRA level depending on experience. QUALIFICATIONS: - Prefer BS/BA and 6months monitoring experience. - Customer service orientation. - Sound knowledge of medical terminology and clinical monitoring process. - Ability to perform regionalized travel an average of 65%, depending on project needs. - Excellent verbal and written communications skills. - Excellent interpersonal and organizational skills and attention to detail. - Computer literacy, proficiency in MS Office. EMAIL RESUME TO dave@davehands.com  CRA, CRA, CRA, Clinical research associate, Regional Monitor, pharmaceutical, biotechnology,  site monitoring, clinical trials, coordinator, clinical research coordinator, kendle, ppd, scirex, covance, quintiles, CRO, clinical research, CRA, CRA, CRA, CRA