University of Pittsburgh
Pittsburgh, Pennsylvania
Biobank Supervisor
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Apply to Biobank Supervisor at University of PittsburghJob details
- Location
- Pittsburgh, Pennsylvania
- Work type
- Onsite
- Posted
- yesterday
- Apply on
- cfopitt.taleo.net
About this role
%3Cp class=%22MsoNormal%22%3EThe University of Pittsburgh, Department of Neurology, would like to hire a qualified Biobank Supervisor (Clinical Research Coordinator).%3Cspan style=%22mso-spacerun:yes;%22%3E%26nbsp;%26nbsp;%3C/span%3E%3C/p%3E%3Cp class=%22MsoNormal%22%3E%3Cspan style=%22font-size:11.0pt;%22%3E%3Cspan style=%22line-height:115%;mso-ascii-font-family:Aptos;mso-bidi-font-family:Aptos;mso-fareast-font-family:%26quot;Times New Roman%26quot;;mso-font-kerning:0pt;mso-hansi-font-family:Aptos;mso-ligatures:none;%22%3EDirects the day-to-day operations of the biobank, ensuring adherence to best practices in biospecimen collection, processing, storage, and utilization of inventory management systems.%3C/span%3E%3C/span%3E%3C/p%3E%3Cul style=%22margin-top:0in;%22 type=%22disc%22%3E%3Cli class=%22MsoNormal%22 style=%22background-color:white;color:#242424;mso-list:l0 level1 lfo1;tab-stops:list .5in;%22%3E%3Cspan style=%22font-size:11.0pt;%22%3E%3Cspan style=%22line-height:115%;mso-ascii-font-family:Aptos;mso-bidi-font-family:Aptos;mso-fareast-font-family:%26quot;Times New Roman%26quot;;mso-font-kerning:0pt;mso-hansi-font-family:Aptos;mso-ligatures:none;%22%3EOversees patient consent processes and documentation, ensuring compliance with IRB protocols, regulatory requirements, and grant-specific guidelines; trains, supervises, and coordinates staff involved in biospecimen collection and handling.%3C/span%3E%3C/span%3E%3C/li%3E%3Cli class=%22MsoNormal%22 style=%22background-color:white;color:#242424;mso-list:l0 level1 lfo1;tab-stops:list .5in;%22%3E%3Cspan style=%22font-size:11.0pt;%22%3E%3Cspan style=%22line-height:115%;mso-ascii-font-family:Aptos;mso-bidi-font-family:Aptos;mso-fareast-font-family:%26quot;Times New Roman%26quot;;mso-font-kerning:0pt;mso-hansi-font-family:Aptos;mso-ligatures:none;%22%3EManages data and sample workflows, including organization, protocol development, quality control, and preliminary analysis of biospecimen data and sample integrity.%3C/span%3E%3C/span%3E%3C/li%3E%3Cli class=%22MsoNormal%22 style=%22background-color:white;color:#242424;mso-list:l0 level1 lfo1;tab-stops:list .5in;%22%3E%3Cspan style=%22font-size:11.0pt;%22%3E%3Cspan style=%22line-height:115%;mso-ascii-font-family:Aptos;mso-bidi-font-family:Aptos;mso-fareast-font-family:%26quot;Times New Roman%26quot;;mso-font-kerning:0pt;mso-hansi-font-family:Aptos;mso-ligatures:none;%22%3ESupervises project budget and supports grant related submissions, while ensuring full compliance with institutional, federal, and sponsor-related requirements.%3C/span%3E%3C/span%3E%3C/li%3E%3C/ul%3E%3Cp%3E%3Cspan style=%22font-family:%26quot;Aptos%26quot;,sans-serif;font-size:12.0pt;%22%3E%3Cspan style=%22line-height:115%;mso-ansi-language:EN-US;mso-ascii-theme-font:minor-latin;mso-bidi-font-family:%26quot;Times New Roman%26quot;;mso-bidi-language:AR-SA;mso-bidi-theme-font:minor-bidi;mso-fareast-font-family:Aptos;mso-fareast-language:EN-US;mso-fareast-theme-font:minor-latin;mso-hansi-theme-font:minor-latin;%22%3EMasters Preferred, Bachelor’s Degree acceptable with 2 years clinical research or laboratory experience.%26nbsp;%3C/span%3E%3C/span%3E%3C/p%3E
*!%3Cp class=%22MsoNormal%22 style=%22mso-layout-grid-align:none;text-autospace:none;%22%3E%3Cspan style=%22font-family:%26quot;ArialMT%26quot;,sans-serif;font-size:11.0pt;%22%3E%3Cspan style=%22line-height:115%;mso-bidi-font-family:ArialMT;mso-font-kerning:0pt;%22%3EPrepares grant applications, performs literature reviews, and prepares manuscripts for publication; writes research papers and assists with writing complex papers. • Oversees and prepares IRB applications. • Reviews/audits research studies; assists with next step determination. • Monitors study budgets and expenditures. Maintains and orders supplies as needed. • Assesses protocol feasibility; establishes protocol-specific recruitment plans.• Trains staff and oversees the work of student workers as directed.• Communicates effectively with study participants and potential community recruits. Identifies community education opportunities. • Facilitates research/project team meetings. • Resolves complex data collection issues. %3C/span%3E%3C/span%3E%3Cspan style=%22font-size:11.0pt;%22%3E%3Cspan style=%22line-height:115%;mso-ascii-font-family:Aptos;mso-bidi-font-family:Aptos;mso-fareast-font-family:%26quot;Times New Roman%26quot;;mso-font-kerning:0pt;mso-hansi-font-family:Aptos;mso-ligatures:none;%22%3EDirects the day-to-day operations of the biobank, ensuring adherence to best practices in biospecimen collection, processing, storage, and utilization of inventory management systems. Oversees patient consent processes and documentation, ensuring compliance with IRB protocols, regulatory requirements, and grant-specific guidelines; trains, supervises, and coordinates staff involved in biospecimen collection and handling.Manages data and sample workflows, including organization, protocol development, quality control, obtain and process lab samples, and preliminary analysis of biospecimen data and sample integrity.%3C/span%3E%3C/span%3E%3C/p%3E%3Cul style=%22margin-top:0in;%22 type=%22disc%22%3E%3Cli class=%22MsoNormal%22 style=%22background-color:white;color:#242424;mso-list:l0 level1 lfo1;tab-stops:list .5in;%22%3E%3Cspan style=%22font-size:11.0pt;%22%3E%3Cspan style=%22line-height:115%;mso-ascii-font-family:Aptos;mso-bidi-font-family:Aptos;mso-fareast-font-family:%26quot;Times New Roman%26quot;;mso-font-kerning:0pt;mso-hansi-font-family:Aptos;mso-ligatures:none;%22%3ESupervises project budget and supports grant related submissions, while ensuring full compliance with institutional, federal, and sponsor-related requirements.%3C/span%3E%3C/span%3E%3C/li%3E%3C/ul%3E%3Cp class=%22MsoNormal%22%3E%26nbsp;%3C/p%3E
*!%3Cp class=%22MsoNormal%22%3E%3Cspan style=%22background-color:white;color:black;font-family:%26quot;Helvetica%26quot;,sans-serif;font-size:10.5pt;%22%3E%3Cspan style=%22line-height:115%;%22%3EModerate physical effort required. May be required to get around a university setting for several hours at a time. May be required to move objects up to 50 pounds with or without assistance of equipment.%3C/span%3E%3C/span%3E%3C/p%3E
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Job Details
Job Description: Med-Neurology, Pennsylvania-Pittsburgh
Assignment Category: Full-time regular
Job Classification: Staff.Clinical Research Coordinator III
Job Family: Research
Job Sub-Family: Clinical Research
Campus: Pittsburgh
Minimum Education Level Required: Master's Degree
Minimum Years of Experience Required: 1
Will this position accept substitution in lieu of education or experience?: Combination of education and relevant experience will be considered in lieu of education and/ or experience requirement.
Work Schedule: M-F, 8:30-5:00
Work Arrangement: On-Campus: Teams that work on campus, in an office, or in a lab.
Hiring Range: TBD Based Upon Qualifications
Relocation Offered: No
Visa Sponsorship Provided: No
Background Check: For position finalists, employment with the University will require successful completion of a background check
Child Protection Clearances: Not Applicable
Required Documents: Resume, Cover Letter
Optional Documents: Not Applicable
Prepares grant applications, manuscripts, Institutional Review Board (IRB) applications, research papers, and assists with complex research papers. Audits research studies, monitors study budgets, resolves complex data collection issues, and implements protocol-specific study recruitment plans. Trains staff and oversees student workers; leads team meetings. Monitors study budgets and orders supplies.
*!%3Cp class=%22MsoNormal%22 style=%22mso-layout-grid-align:none;text-autospace:none;%22%3E%3Cspan style=%22font-family:%26quot;ArialMT%26quot;,sans-serif;font-size:11.0pt;%22%3E%3Cspan style=%22line-height:115%;mso-bidi-font-family:ArialMT;mso-font-kerning:0pt;%22%3EPrepares grant applications, performs literature reviews, and prepares manuscripts for publication; writes research papers and assists with writing complex papers. • Oversees and prepares IRB applications. • Reviews/audits research studies; assists with next step determination. • Monitors study budgets and expenditures. Maintains and orders supplies as needed. • Assesses protocol feasibility; establishes protocol-specific recruitment plans.• Trains staff and oversees the work of student workers as directed.• Communicates effectively with study participants and potential community recruits. Identifies community education opportunities. • Facilitates research/project team meetings. • Resolves complex data collection issues. %3C/span%3E%3C/span%3E%3Cspan style=%22font-size:11.0pt;%22%3E%3Cspan style=%22line-height:115%;mso-ascii-font-family:Aptos;mso-bidi-font-family:Aptos;mso-fareast-font-family:%26quot;Times New Roman%26quot;;mso-font-kerning:0pt;mso-hansi-font-family:Aptos;mso-ligatures:none;%22%3EDirects the day-to-day operations of the biobank, ensuring adherence to best practices in biospecimen collection, processing, storage, and utilization of inventory management systems. Oversees patient consent processes and documentation, ensuring compliance with IRB protocols, regulatory requirements, and grant-specific guidelines; trains, supervises, and coordinates staff involved in biospecimen collection and handling.Manages data and sample workflows, including organization, protocol development, quality control, obtain and process lab samples, and preliminary analysis of biospecimen data and sample integrity.%3C/span%3E%3C/span%3E%3C/p%3E%3Cul style=%22margin-top:0in;%22 type=%22disc%22%3E%3Cli class=%22MsoNormal%22 style=%22background-color:white;color:#242424;mso-list:l0 level1 lfo1;tab-stops:list .5in;%22%3E%3Cspan style=%22font-size:11.0pt;%22%3E%3Cspan style=%22line-height:115%;mso-ascii-font-family:Aptos;mso-bidi-font-family:Aptos;mso-fareast-font-family:%26quot;Times New Roman%26quot;;mso-font-kerning:0pt;mso-hansi-font-family:Aptos;mso-ligatures:none;%22%3ESupervises project budget and supports grant related submissions, while ensuring full compliance with institutional, federal, and sponsor-related requirements.%3C/span%3E%3C/span%3E%3C/li%3E%3C/ul%3E%3Cp class=%22MsoNormal%22%3E%26nbsp;%3C/p%3E
*!%3Cp class=%22MsoNormal%22%3E%3Cspan style=%22background-color:white;color:black;font-family:%26quot;Helvetica%26quot;,sans-serif;font-size:10.5pt;%22%3E%3Cspan style=%22line-height:115%;%22%3EModerate physical effort required. May be required to get around a university setting for several hours at a time. May be required to move objects up to 50 pounds with or without assistance of equipment.%3C/span%3E%3C/span%3E%3C/p%3E
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The University of Pittsburgh is an equal opportunity employer / disability / veteran.
Job Details
Job Description: Med-Neurology, Pennsylvania-Pittsburgh
Assignment Category: Full-time regular
Job Classification: Staff.Clinical Research Coordinator III
Job Family: Research
Job Sub-Family: Clinical Research
Campus: Pittsburgh
Minimum Education Level Required: Master's Degree
Minimum Years of Experience Required: 1
Will this position accept substitution in lieu of education or experience?: Combination of education and relevant experience will be considered in lieu of education and/ or experience requirement.
Work Schedule: M-F, 8:30-5:00
Work Arrangement: On-Campus: Teams that work on campus, in an office, or in a lab.
Hiring Range: TBD Based Upon Qualifications
Relocation Offered: No
Visa Sponsorship Provided: No
Background Check: For position finalists, employment with the University will require successful completion of a background check
Child Protection Clearances: Not Applicable
Required Documents: Resume, Cover Letter
Optional Documents: Not Applicable
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