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Washington University of St. Louis Clinical Research Coordinator II - Pediatrics Rheumatology - 47654 in St. Louis, Missouri

Job Type/Schedule

This position is full-time and works approximately 40 hours per week.

Department Name/Job Location

This position is in the Department of Pediatrics Rheumatology. The position is located at the Northwest Tower. This position is for the Medical School Campus.

Essential Functions

POSITION SUMMARY:

This individual will assists investigators as coordinator of complex clinical research projects focused on Pediatric Immunology and Rheumatology diseases including genetic studies. They may be responsible for multiple research studies simultaneously, acting as a liaison with the school, sponsoring agency, community and the study participants; responsible for managing and recording all phases of study protocol as required by sponsoring agency to ensure compliance. They will be expected to coordinate and write study protocols with investigators, screen and enroll participants and their family members at this institution and in collaboration with other institutions, document study procedures and data, work collaboratively with a clinical and research team. They should be comfortable talking to children and their families who may be ill and in the clinic or inpatient setting. This position will also include drawing blood samples from patients after appropriate training.

PRIMARY DUTIES AND RESPONSIBILITIES:

  1. 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.
  2. Coordinates the development of forms, questionnaires, and the application of research techniques; assists in writing instructional procedure manuals for study progress, data collection and coding; reviews journals, abstracts and scientific literature to keep abreast of new developments and to obtain information regarding previous studies to aid in the planning of new studies.
  3. Routinely implements and manages all phases of study/protocol; ensures compliance with protocol guidelines and requirements of regulatory agencies; establishes record-keeping systems; makes assessments and determinations of participants’ progress in the study; analyzes, investigates, and reports adverse events; makes decisions as when to notify physicians of issues, when to stop participant inclusion, and/or to make and/or recommend adjustment of the protocol of particular participants; resolves IRB/protocol management issues and recommends corrective action as appropriate; serves as liaison with funding or sponsoring agency.
  4. Evaluates and interprets collected clinical data in conjunction with PI as appropriate; prepares oral or written presentations or reports and analyses setting forth progress trends and provides recommendations or conclusions of the same.
  5. Performs other duties incidental to the work described herein including recruiting participants, working to coordinate sample collections and coordinating processing with the research laboratory, working with outside institutions on multi-center studies and coordinating consent and sample collection from those participants.

Required Qualifications

Bachelor’s degree plus a minimum of two years of clinical research experience; a combination of relevant work and education equaling six years may substitute for this requirement.

Preferred Qualifications

  • Experience consenting participants for research studies in an academic research setting.
  • Experience with genomic studies and basic understanding of genetics.
  • Experience drawing blood.
  • Working knowledge of techniques and methodologies used in developing, coordinating, and managing clinical research projects with working knowledge of database management, spreadsheet and statistical analysis software.

Salary Range

The hiring range for this position is $48,131 - $60,174 annually.

Pre-Employment Screening

All external candidates receiving an offer for employment will be required to submit to pre-employment screening for this position. Current employees applying for a new position within the university may be subject to this requirement. The screenings will include a criminal background check and, as applicable for the position, other background checks, drug screen, employment and education or licensure/certification verification, physical examination, certain vaccinations and/or governmental registry checks. All offers are contingent upon successful completion of required screening.

Benefits

This position is eligible for full-time benefits. Please click the following link to view a summary of benefits: https://wustl.box.com/s/8wkhs25yssf0775x9d6nd6vqa7obpth7.

EOE Statement

Washington University is an Equal Opportunity Employer. All qualified applicants will receive consideration for employment without regard to race, color, religion, age, sex, sexual orientation, gender identity or expression, national origin, genetic information, disability, or protected veteran status.

Job Title: Clinical Research Coordinator II - Pediatrics Rheumatology - 47654

Job ID: 47654

Location: Medical School

Full/Part Time: Full-Time

Regular/Temporary: Regular

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