Job Listing
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| Job ID: 14042628 |
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| Job Location: |
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| How to Apply: | To see employer contact information, log in or register. |
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| Job Title: | Clinical Research Coordinator 1- PACCS |
| Work Type: | Work Days: Work Vary: Yes , Shift: Other, Hours Per Week: 40, Work Type: Regular |
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| Salary Offered: | Unspecified |
| Benefits: | Unspecified. |
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| Physical Required: | Unspecified |
| Drug Testing Required: | Unspecified |
| Education Required: | Bachelor's Degree |
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| Experience Required: | Unspecified |
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| Required Skills: | Please see the job description for information about required job skills. |
| Preferred Skills: |
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| Job Description: |
Job ID360785
LocationTwin Cities
Job FamilyResearch-Support
Full/Part TimeFull-Time
Regular/TemporaryRegular
Job Code8352P1
Employee ClassCivil Service
About the Job
The primary purpose of this position is to support University faculty performing clinical research in the understanding and treatment of diseases in Pulmonary, Critical Care, Allergy, and Sleep Medicine. Duties are determined by protocol-specific requirements and may include any research activity from protocol development through study closeout. This position reports to the Research Manager, but is accountable to the physician-investigators, program leaders, and members of the clinical research team. The Clinical Research Coordinator fulfills a dynamic and integral role as a key player in the research team.
RESPONSIBILITIES/DUTIES
Protocol/Participant Management (80%)
Adhere to local and federal policies for conducting research and documentation of study activities.
Recruit interested individuals to participate in research projects in accordance with the IRB approved protocol processes and study documents.
Engage with the research team in verifying subject eligibility, facilitating subject enrollments, and ensuring compliant completion of research activities.
Schedule appointments with participants and assessment staff per protocols. Provide participants with instructions and materials needed to prepare for the visit. Remind participants of upcoming visits using approved communication methods.
Prepare for study appointments per protocol by: reserving rooms and equipment; printing off forms; creating participant profiles within data capture systems; charging equipment; and other tasks as needed.
Obtain informed consent and assent, including assessments of capacity to consent to research. Re-consent participants as needed after protocol modifications.
Communicate with principal investigator/study team to ensure study specific procedures are completed.
Collect data and conduct assessments as part of study specific visits, in-person or remotely, as needed per protocol specific guidelines, including data abstraction from medical records using standard forms.
Assist with other documentation as directed such as procure outside medical records or documenting participant study-related visits in medical chart.
Support timely and quality data submission; engage with providers and investigators to ensure adequate source documentation is available; accurate interpretation and recording of data including lab/imaging results; maintenance of subject research charts.
Complete required forms for any adverse events, serious or otherwise, and report and notify appropriate individuals/entities per research requirements.
Use University systems such as Florence, OnCore, Box, and REDCap to maintain information for all necessary research documentation.
Assist in ordering and management of study supplies, as needed.
Provide information to University faculty and staff for protocol specific queries, including availability of trials, enrollment requirements, specimens needed, etc.
Effectively work independently in multiple locations with hospital and clinic staff to complete research related tasks
Research Regulatory Management (15%)
Support the completion of required regulatory documentation and other regulatory tasks as needed
In collaboration with the research team, interpret study protocols and inform the development of consent forms and other materials needed for each clinical research study
Coordinate with Regulatory Specialists or Project Managers for submission of modifications to IRB for review. Support responses to clarification questions or stipulations from the IRB, as required.
Implement updates to materials after protocol modifications are approved (e.g., update consent forms to the approved version)
Maintain regulatory documents, such as: enrollment logs; participant visit logs; protocol deviation logs; personnel training records
Other Duties Assigned (5%)
Administrative responsibilities such as communication coordination.
Qualifications
Required qualifications:
BA/BS or a combination of related education and work to equal 4 years of experience in a clinical or research setting in related field.
Computer proficiency and ability to navigate multiple software applications (Microsoft Word, Excel and REDCap)
Demonstrated ability to maintain deadlines and prioritize assignments
Excellent written, verbal and interpersonal communication skills
Preferred Qualifications:
Knowledge of clinical research compliance standards, e.g. informed consent process, adverse event reporting, the Federal Code of Regulations and Good Clinical Practices (GCP) Standards
Demonstrated data management skills, such as data collection, data entry and quality control
Detail-oriented with strong organizational, planning and problem-solving skills
About the Department
Committed to innovation and diversity, the Medical School educates physicians, scientists, and health professionals; generates knowledge and treatments; and cares for patients and communities with compassion and respect. We value excellence, inclusiveness, collaboration, and discovery.
The mission of the regional campus located in Duluth is to be a national leader in improving healthcare access and outcomes in rural Minnesota and American Indian/Alaska Native (AI/AN) communities. In partnership with CentraCare, the regional campus in St. Cloud offers a wide range of patient experiences throughout students' education in Greater Minnesota and prepares them to become exceptional clinicians and leaders for rural and immigrant populations.
Benefits
Working at the University
At the University of Minnesota, you'll find a flexible work environment and supportive colleagues who are interested in lifelong learning. We prioritize work-life balance, allowing you to invest in the future of your career and in your life outside of work.
The University also offers a comprehensive benefits package that includes:
Competitive wages, paid holidays, and generous time off
Continuous learning opportunities through professional training and degree-seeking programs supported by the
Low-cost medical, dental, and pharmacy plans
Healthcare and dependent care flexible spending accounts
University HSA contributions
Disability and employer-paid life insurance
Employee wellbeing program
Excellent retirement plans with employer contribution
Public Service Loan Forgiveness (PSLF)
Financial counseling services
Employee Assistance Program with eight sessions of counseling at no cost
with free or reduced rates in the Twin Cities metro area
Please visit the for more information regarding benefits.
How To Apply
Applications must be submitted online. To be considered for this position, please click the Apply button and follow the instructions. You will be given the opportunity to complete an online application for the position and attach a cover letter and resume.
Additional documents may be attached after application by accessing your "My Job Applications" page and uploading documents in the "My Cover Letters and Attachments"... For full info follow application link.
The University recognizes and values the importance of diversity and inclusion in enriching the employment experience of its employees and in supporting the academic mission. The University is committed to attracting and retaining employees with varying identities and backgrounds.
The University of Minnesota provides equal access to and opportunity in its programs, facilities, and employment without regard to race, color, creed, religion, national origin, gender, age, marital status, disability, public assistance status, veteran status, sexual orientation, gender identity, or gender expression. To learn more about diversity at the U: http://diversity.umn.edu.
Refer to ID 79153644 when applying |
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