Clinical Research Coordinator
Location: Salt Lake City, Utah
Description: UtahTechnologyJobs.com is at the momment seeking for Clinical Research Coordinator right now, this career will be ordered in Utah. Further informations about this career opportunity please give attention to these descriptions. DESCRIPTION
The Pediatric Clinical Trials Office has an opening for a Clinical Research Coordinator to provide multi-departmental research support. This! position will be responsible for coordinating the implementation, quality control and completion of research studies while assisting the Principal Investigator in determining and accomplishing study objectives. The position will also oversee research studies in an administrative and operational capacity while maintaining compliance with guidelines set by governing agencies.
University of Utah Job ID PRN04442B
DUTIES
1. Oversees compliance to protocol; manages quality control, completion and submission of study related documentation; prepares reports for organizations and agencies.
2. May assist in developing study budgets and monitoring budget expenses and billing for allied services.
3. Monitors enrollment goals and initiates strategies to promote enrollment and participant compliance. Coordinates and performs responsibilities related to research participants including determining subject population availability, developing informed cons! ents and screening materials, screening and recruiting subject! s, scheduling visits, obtaining informed consent, answering subject inquiries, overseeing study visits and acting as a liaison between participants and study-related parties.
4. Recognizes, tracks and reports adverse events and protocol deviations.
5. Prepares for and coordinates site visits made by sponsors or federal agencies during the course of and at the close of the study.
6. Prepares, submits and maintains IRB, FDA, NCI, NIH, NSF and/or other regulatory documents and research correspondence.
7. Develops and maintains patient databases, investigational logs and records of drugs administered, medical devices monitored and/or procedures followed.
8. May assist the Principal Investigator in the development of study materials.
QUALIFICATIONS
Bachelors degree in a health sciences or related field with two years professional research experience and completion of University RATS Clinical Certification within one year of hire required. Ex! ceptional organizational skills, attention to detail, and demonstrated human relations and effective communication skills also required.
Knowledge of Good Clinical Practices, FDA, HIPAA and IRB regulations; an understanding of research procedures; and the ability to function independently is preferred.
TO APPLY, VISIT:
http://utah.peopleadmin.com/postings/26570
EQUAL EMPLOYMENT OPPORTUNITY
The University of Utah is an Affirmative Action/Equal Opportunity employer. Upon request, reasonable accommodations in the application process will be provided to individuals with disabilities. The University of Utah is committed to diversity in its workforce. Women and minorities are encouraged to apply. 1. Oversees compliance to protocol; manages quality control, completion and submission of study related documentation; prepares reports for organizations and agencies.
2. May assist in developing study budgets and monitoring budget expenses a! nd billing for allied services.
3. Monitors enrollment goals and in! itiates strategies to promote enrollment and participant compliance. Coordinates and performs responsibilities related to research participants including determining subject population availability, developing informed consents and screening materials, screening and recruiting subjects, scheduling visits, obtaining informed consent, answering subject inquiries, overseeing study visits and acting as a liaison between participants and study-related parties.
4. Recognizes, tracks and reports adverse events and protocol deviations.
5. Prepares for and coordinates site visits made by sponsors or federal agencies during the course of and at the close of the study.
6. Prepares, submits and maintains IRB, FDA, NCI, NIH, NSF and/or other regulatory documents and research correspondence.
7. Develops and maintains patient databases, investigational logs and records of drugs administered, medical devices monitored and/or procedures followed.
8. May assist the Princi! pal Investigator in the development of study materials.
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This career will be opened on: Sun, 08 Sep 2013 08:36:21 GMT
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