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Clinical Research Coordinator

  • Location: Baltimore, Baltimore, Maryland
  • Job Type:Contract

Posted 7 days ago

  • Sector: Government
  • Start Date: 2022-06-21
  • Job Ref: 22-12854
Proposal Due Date ~No incumbent~
Jul 4, 2022 5:00 PM
Position Number
Job Title
Labor Category
Number of Positions
NIDA-223393-1
Clinical Research Coordinator
Clinical Research Coordinator 1 - 6
1
NIDA
Location
Baywiew Blvd Bldg: BRC-200, Room: Suite 200 Baltimore, MD 21224
Weekly Hours FT: 30-40 hours per week
Number of Hours 40
SHIFT SCHEDULE
On-Call or Rotational Shifts No
Teleworking Eligible Yes
Nights Yes
Holidays Yes
Fixed Schedule No
Overall Position Summary and Objectives Under this task order, the contractor will independently provide support services to satisfy the overall operational objectives of the National Institute on Drug Abuse. The primary objective is to provide services and deliverables through performance of support services.
Minimum Education
Bachelor's
Resume Max Pages
3
Certifications & Licenses
* Master's degree in Psychology, Social Work or a related discipline
* BA/BS
* Yearly renewal of Clinical Research Coordinator Certification
Skills (Ranked By Priority)
1. experience in human subjects interaction (clinical or research).
2. Strong communications skills, both oral and written
1, 2, 3, 4, 5 _represents priority rankings, where 1 is highest priority and 5 is lowest priority of those ranked_
Software
* MS Office Suite
Field of Study
* Medical Technologies Technicians
DELIVERABLES
* Work products and documents related to developing and maintaining research protocols; participate in subject recruitment and retention; educate participants on research protocols; obtain informed consent from participants. - Ad-Hoc
* Work products and documents related to training participants on cognitive tasks specific to protocols; perform study testing and observations duties; obtain and process specimen; destroy specimens as needed; maintain storage records/inventory of biological specimens. - Ad-Hoc
* Work products and documents related to acquainting participants with scanner; perform research related manipulations during MRI experiments. - Ad-Hoc
* Work products and documents related to creating data spreadsheets; enter data; provide guidance to staff and on IRB document preparation; provide data back-up for MRI scanning experiments; participate in data analysis. - Ad-Hoc
* Participate in subject recruitment activities and outreach events' - Ad-Hoc
STATEMENT OF WORK DETAILS
functional responsibility
Other
description
* Collaborate with staff on developing and maintaining research protocols
1
description
* Obtain and process biological specimens
description
* Destroy biological specimens as needed
description
* Work with staff on subject recruitment and retention
2
description
* Maintain storage recordsinventory of biological specimens
description
* Educate participants on research protocols
3
description
* Acquaint participants with scanner and increase their comfort level with the researchexperience
description
* Perform research related manipulations eg help load subject in scanner, prepareand operate computer-based data acquisition and task delivery during MRI basedexperiments
description
* Obtain informed consent from participants in protocols
description
* Create data spreadsheets
description
* Train participants on cognitive tasks specific to protocols
description
* Perform study testing, observations data entry and other duties associated with studysessions
description
* Enter research data on associated reports and spreadsheets
description
* Provide guidance to other research associates or student interns
description
* Provide guidance on IRB document preparation
description
* Provide data back-up for all MRI scanning experiments
description
* Participate in data analysis
1, 2, 3, 4, 5 _represents priority rankings, where 1 is highest priority and 5 is lowest priority of those ranked_