Pediatric Project Manager I
Location: Salt Lake City, Utah
Description: UtahTechnologyJobs.com is currently interviewing Pediatric Project Manager I right now, this vacancy will be delegated in Utah. More details about this vacancy opportunity kindly read the description below. DESCRIPTION
The Data Coordinating and Analysis Center (DCAC) at the University of Utah, Division of Pediatric Critical Care is seeking a Project Manager I to assist in the im! plementation of several clinical research projects for the Network of Pediatric Multiple Sclerosis Centers (NPMSC). The Project Manager I, under the guidance of the Program Director, will be responsible for the management of NPMSC research projects across multiple clinical sites.
University of Utah Job ID PRN03494B
DUTIES
- Under guidance of the Program Manager, responsible for providing oversight for all aspects of study conduct, regulatory compliance and record keeping for the participating clinical centers.
- Coordinating and tracking protocol and amendment release, consent form changes, IRB submissions and IRB question resolution with clinical centers.
- Preparing, submitting and maintaining study IRB approval, regulatory and other research correspondence.
- Preparing study materials including the Manual of Operations, Data collection worksheets and training materials.
- Assuring that adverse events are repor! ted in accordance with the protocol.
- Assisting progra! mmers and data managers in developing and testing data collection and reporting tools.
- Reviewing incoming data to identify trends, problems or other issues.
- Ensuring that data is captured accurately and assisting in correcting erroneous or conflicting data.
- Communicating with participating sites frequently to discuss study conduct and to follow up on data issues; assisting with troubleshooting possible solutions.
- Communicating between clinical center personnel, lead study PIs and the NPMSC Steering Committee regarding data definition questions and study issues.
- Conducting coordinator calls with all participating sites to disseminate study information.
- Organizing study trainings and giving presentations to the NPMSC on study procedure implementation and Good Clinical Practice.
- Performing remote monitoring of site data in coordination with appropriate personnel.
- Attending required trainings, conferences a! nd meetings as appropriate.
- Licensed professionals may be assigned medical review responsibilities.
Bachelors degree in a health science field, or equivalency AND 2 years of clinical research experience. Experience with human subjects research preferred. Must have excellent interpersonal and communication skills, both oral and written. Must be proficient in Microsoft Office and possess the ability to learn new software programs.
Credentialing as a Certified Clinical Research Coordinator (CCRC), Certified Clinical Research Professional (CCRP), Certified Clinical Research Associate (CCRA), or other related certification is highly preferred, along with experience in the specific clinical research area. Working knowledge of FDA, ICH, and other regulatory compliance preferred.
TO APPLY, VISIT:
http://utah.peopleadmin.com/postings/22553
Equal Employment Opportunity
The University of Utah is an A! ffirmative Action/Equal Opportunity employer. * Under guidance of the P! rogram Manager, responsible for providing oversight for all aspects of study conduct, regulatory compliance and record keeping for the participating clinical centers.
- Coordinating and tracking protocol and amendment release, consent form changes, IRB submissions and IRB question resolution with clinical centers.
- Preparing, submitting and maintaining study IRB approval, regulatory and other research correspondence.
- Preparing study materials including the Manual of Operations, Data collection worksheets and training materials.
- Assuring that adverse events are reported in accordance with the protocol.
- Assisting programmers and data managers in developing and testing data collection and reporting tools.
- Reviewing incoming data to identify trends, problems or other issues.
- Ensuring that data is captured accurately and assisting in correcting erroneous or conflicting data.
- Communicating with participating! sites frequently to discuss study conduct and to follow up on data issues; assisting with troubleshooting possible solutions.
- Communicating between clinical center personnel, lead study PIs and the NPMSC Steering Committee regarding data definition questions and study issues.
- Conducting coordinator calls with all participating sites to disseminate study information.
- Organizing study trainings and giving presentations to the NPMSC on study procedure implementation and Good Clinical Practice.
- Performing remote monitoring of site data in coordination with appropriate personnel.
- Attending required trainings, conferences and meetings as appropriate.
- Licensed professionals may be assigned medical review responsibilities.
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If you were eligible to this vacancy, please deliver us your resume, with salary requirements and a resume to UtahTechnologyJobs.com.
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This vacancy will be opened on: Wed, 08 May 2013 17:18:15 GMT
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