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Clinical Research Specialist - Pathology and Immunology
Washington University in St. LouisSteven & Susan Lipstein BJC Institute of Health, United States, United Statesfull_timeVerifiedPosted 19 Nov 2025
💰 $105,500/yr($68,100/yr – $105,500/yr)
About the role
Scheduled Hours
40Position Summary
The Pathology Research Collaborative is seeking a clinical research specialist to help oversee and coordinate complex clinical research studies. The ideal candidate will serve as a resource to provide comprehensive information to clinical research staff by promoting a smooth operation of clinical research. They will work collaboratively with multiple faculty members to ensure study start-up and completion and will be responsible for preparation of budgetary reports and ensures billing and regulatory compliance standards are maintained.Job Description
Primary Duties & Responsibilities:
- Assists in protocol development, budget development, dispensing of study funds for multi-clinical research projects; provides high level of direct and indirect support direct.
- Works with PI to design, perform and evaluate research procedures; confers with PI to assist in developing plans for research projects and discuss the interpretation of results; collaborates in the preparation of manuscripts for publications and preparation of grant proposals to sponsoring agencies; assists in the preparation of amendments to protocols and/or modifications to study design as appropriate.
- Directs the planning, implementation and coordination of clinical trials sponsored by industry, government, non-profit foundations, or private organizations and serves as the established point of contact for the study; prompts communications to ensure the shortest possible timeframes for start-up.
- Tracks in a coordinated manner the IRB approval process, contract execution, ancillary approvals, credentialling requirements, regulatory documents, and other study-start-up requirements in partnership with the study PI and study team.
- Serves as a resource to the clinical research staff, ensuring appropriate procedures and explains policies and procedures; ensures that research projects are completed according to IRB and federal guidelines.
- Develops and implements policies and procedures; provides comprehensive direction to clinical research personnel; may participate in the hiring, training and evaluation of clinical research staff.
- Provides Study Coordinator functions and performs all duties associated with the coordination and implementation of clinical research study/projects, data collection and the management of data generated by study protocols.
- Researches and recommends new methods and procedures to maintain standards and improve quality.
Required Qualifications
Education:
Bachelor’s degree or combination of education and/or experience may substitute for minimum education.
Certifications/Professional Licenses:
Work Experience:
Skills:
Driver's License:
More About This Job
Required Qualifications:
- Basic Life Support certification must be obtained within one month of hire date.
- Basic Life Support certification (Online BLS certifications, those without a skills assessment component, are not sufficient to meet the BLS requirements).
Preferred Qualifications
Education:
No additional education unless stated elsewhere in the job posting.
Certifications/Professional Licenses:
Work Experience:
Skills:
Analytical Thinking, Clinical Research, Interpersonal Communication, Leadership, Oral Communications, Prioritization, Problem Solving, Written CommunicationGrade
C13Salary Range
$68,100.00 - $105,500.00 / AnnuallyThe salary range reflects base salaries paid for positions in a givenApply for this role
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