Research Associate III jobs in United States
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CHEManager International · 4 hours ago

Research Associate III

Parsons is a company that values people and fosters growth, and they are seeking a Research Associate III to support research efforts at the Naval Medical Research Unit - San Antonio. The role involves coordinating clinical research studies, maintaining regulatory requirements, and overseeing junior-level personnel.

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Responsibilities

Assist with the collection of supporting documentation for requirement packages, IACUC/IRB protocols, research proposals and protocols, manuscripts, SOPs, reports, and presentation editing/review
Assist Government personnel in initiating and maintaining regulatory IACUC/IRB requirements
Develop and coordinate the implementation of clinical research studies, including regulatory requirements, maintenance of study records, and all activities associated with internal and external audits
Assist in ordering supplies for research under contract for animal procurement, subject to final Government approval
Assist in maintaining inventory of supplies for research under contract
Modify and plan research experiment schedules, procedures, and tests
Assist in the maintenance of a clean and operational lab space
Develop, organize, and maintain the study database and data validation
Maintain data and records securely, including the use of an assigned laboratory notebook
Write and edit research material for publication and presentation
Oversee the work of junior-level contract personnel
Assist the Principal Investigator (PI) in tracking and updating established project budgets
Assist the Government Support Agreements Manager with support agreements. All formal communication shall come from the Government Support Agreements Manager

Qualification

Clinical research coordinationRegulatory requirements maintenanceStudy database developmentProject documentation managementEditing skillsMentoring junior personnelOrganizational skills

Required

Bachelor's degree plus ten (10) years' related experience or a master's degree plus three (3) years' related experience
Demonstrated ability to coordinate clinical research studies and maintain regulatory requirements
Proficiency in developing and maintaining study databases and data validation
Strong organizational skills for managing project documentation and inventory
Excellent writing and editing skills for research material and presentations
Ability to oversee and mentor junior-level contract personnel

Benefits

Medical
Dental
Vision
Paid time off
401(k)
Life insurance
Flexible work schedules
Holidays

Company

CHEManager International

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Wiley’s leading media brand providing first-hand information on the global chemical, life science and process industries

Funding

Current Stage
Growth Stage
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