Clinical Research Coordinator I - Pediatric Endocrinology
Washington University in St. Louis
LocationSAINT LOUIS, MO 63110Scheduled Hours40Position SummaryWe are seeking a motivated, detail-orientated Clinical Research Coordinator to assist investigators as coordinator of basic to moderately complex clinical research studies; 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 the sponsoring agency to ensure compliance.As part of the study team, you will interact with both pediatric participants and their families. Key responsibilities include participant screening and enrollment, scheduling and conducting study visits, collecting tracking and managing initial antibody screening tests and results, data entry, regulatory and study management, and other various coordinating activities.Job DescriptionPrimary Duties & Responsibilities:Implements and manages all phases of clinical research studies, protocols, and related program activities; ensures compliance with protocol guidelines and requirements of regulatory agencies and sponsoring organizations; establishes and maintains appropriate record-keeping systems; monitors participants’ progress and study activities; analyzes, investigates and reports adverse events; makes decisions as to 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 protocol management issues and recommends corrective action as appropriate; serves as liaison with investigators, clinical teams, funding or sponsoring agency, and study participants and families.Recruits and enrolls study participants and/or facilities participation in research and screening activities; makes and/or participates in making determinations of eligibility based on established study criteria and participant information; develops and/or maintains study materials and informed consent documentation, as applicable; communicates with study participants and families regarding study purpose, procedures, screening opportunities, and visit requirements; address routine participant and family questions and facilitates communication with appropriate clinical or research personnel.Ensures timely completion of all protocol and program requirements, including assessment, laboratory testing, procedures, visits, and follow-up activities; coordinates study and/or screening activities, results, and follow-up requirements, as applicable; evaluates and interprets collected clinical data as appropriate; prepares oral or written presentations or reports summarizing study or program activities and progress. Collects, enters, maintains, and manages clinical and research data in accordance with approved protocols and established data-management procedures, including maintaining study-specific databases and tracking participant, laboratory, screening, and follow-up information, as applicable.Performs other duties as assigned.Working Conditions:Job Location/Working Conditions:Patient care setting.Physical Effort:Typically sitting at desk or table.Equipment:Office equipment.The above statements are intended to describe the general nature and level of work performed by people assigned to this classification. They are not intended to be construed as an exhaustive list of all job duties performed by the personnel so classified. Management reserves the right to revise or amend duties at any time.Required QualificationsEducation:Bachelor’s degree or combination of education and/or experience may substitute for minimum education.Certifications /Professional Licenses :The list below may include all acceptable certifications, professional licenses and issuers. More than one credential, certification or professional license may be required depending on the role.Basic Life Support - American Heart Association, Basic Life Support - American Red CrossWork Experience:No specific work experience is required for this position.Skills:Not ApplicableDriver's License:A driver's license is not required for this position.More About This JobRequired Qualifications:Basic Life Support certification (Online BLS certifications, those without a skills assessment component, are not sufficient to meet the BLS requirements).Preferred QualificationsEducation:No additional education unless stated elsewhere in the job posting.Certifications /Professional Licenses :No additional certification/professional licenses unless stated elsewhere in the job posting.Work Experience:No additional work experience unless stated elsewhere in the job posting.Skills:Clinical Research, Clinical Study Protocols, Communication, Computer Systems, Interpersonal Communication, Organizing, Research SupportGradeC09Salary Range$49,200.00 - $73,800.00 / AnnuallyThe salary range reflects base salaries paid for positions in a given job grade across the University. Individual rates within the range will be determined by factors including one's qualifications and performance, equity with others in the department, market rates for positions within the same grade and department budget.QuestionsFor frequently asked questions about the application process, please refer to our External Applicant FAQ .AccommodationIf you are unable to use our online application system and would like an accommodation, please email View email address on click.appcast.io or call the dedicated accommodation inquiry number at View phone number on click.appcast.io and leave a voicemail with the nature of your request.All qualified individuals must be able to perform the essential functions of the position satisfactorily and, if requested, reasonable accommodations will be made to enable employees with disabilities to perform the essential functions of their job, absent undue hardship.Pre-Employment ScreeningAll external candidates receiving an offer for employment will be required to submit to pre-employment screening for this position. The screenings will include criminal background check and, as applicable for the position, other background checks, drug screen, an 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 StatementPersonalUp to 22 days of vacation, 10 recognized holidays, and sick time.Competitive health insurance packages with priority appointments and lower copays/coinsurance.Take advantage of our free Metro transit U-Pass for eligible employees.WashU provides eligible employees with a defined contribution (403(b)) Retirement Savings Plan, which combines employee contributions and university contributions starting at 7%.WellnessWellness challenges, annual health screenings, mental health resources, mindfulness programs and courses, employee assistance program (EAP), financial resources, access to dietitians, and more!FamilyWe offer 4 weeks of caregiver leave to bond with your new child. Family care resources are also available for your continued childcare needs. Need adult care? We’ve got you covered.WashU covers the cost of tuition for you and your family, including dependent undergraduate-level college tuition up to 100% at WashU and 40% elsewhere after seven years with us.For policies, detailed benefits, and eligibility, please visit: StatementWashington University in St. Louis is committed to the principles and practices of equal employment opportunity. It is the University’s policy to provide equal opportunity and access to persons in all job titles without regard to race, ethnicity or shared ancestry, color, national origin, citizenship (where prohibited by federal law), age, religion, sex, sexual orientation, gender identity or expression, disability, protected veteran status, or genetic information. As a federal contractor, the university maintains affirmative action programs to implement its equal employment opportunity policy for individuals with disabilities and protected veterans, in accordance with Section 503 of the Rehabilitation Act of 1973, as amended, and the Vietnam Era Veterans’ Readjustment Assistance Act of 1974 (VEVRAA), as amended. #J-18808-Ljbffr Washington University in St. Louis
$54.6k - $81.9k
...Location: SAINT LOUIS, MO 63110 | Scheduled Hours: 40 Position Summary Position within the Pediatrics Clinical Research Unit (PCRU) assists investigators as coordinator of complex clinical research studies; responsible for multiple research studies simultaneously,...SuggestedWork experience placementWork at office- Washington University in St. Louis is seeking a part-time Clinical Research Coordinator I to support day-to-day coordination of ECMO and HD-DOT studies in critically ill pediatric participants. The role acts as liaison with the school, sponsors, community, and study participants...SuggestedPart time
- Washington University in St. Louis is seeking a research coordinator for the WashU Medicine Center for Pediatric Neuromuscular Disorders. This role involves managing clinical studies and ensuring compliance with protocol guidelines. Candidates must possess a Bachelor's...Suggested
$58.3k - $90.4k
...Holtz lab is seeking help with a complex observational clinical study at Washington University School of Medicine. The... ...from their pets. In this position, you will oversee and coordinate a complex clinical research study; serve as a resource to provide comprehensive information...SuggestedWork experience placementWork at officeFlexible hours$58.3k - $90.4k
Position Summary Position oversees and coordinates complex or multi-site clinical research studies; serves as a resource to provide comprehensive information to clinical research staff by promoting a smooth operation, preparation of regulatory compliance and interaction...SuggestedWork experience placementWork at office$64.3k - $99.7k
...108 Scheduled Hours 40 Position Summary The Cruchaga lab at the NeuroGenomics and Informatics Center is hiring a Senior Clinical Research Coordinator. This person will oversee and coordinate complex or multi-site clinical research studies, serve as a resource to provide...Work experience placementWork at office- ...Washington University in St. Louis seeks a Clinical Research Coordinator to manage study protocols, ensure regulatory compliance, and coordinate participant activities across visits and assessments. You will document progress, report adverse events, obtain informed...
- ## Clinical Research Coordinator I - SurgeryApplyremote type: On Campus/Onsitelocations: Washington University Medical Campustime type: Full timeposted on: Posted Todayjob requisition id: JR95514# **Scheduled Hours**40# **Position Summary**Assists investigators as coordinator...Work experience placementWork at office
- ...Clinical Research CoordinatorEyeCare Partners is the nation's leading provider of clinically integrated eye care. Our national network of... ...part-time during the school year.Job Title: Clinical Research Coordinator Company: Ophthalmology Associates Location: Des Peres, MO...Full timeContract workPart timeSummer workWork at officeMonday to Friday
$23.63 - $35.49 per hour
...Washington University in St. Louis is seeking a Clinical Research Coordinator I to assist in managing clinical research studies. Responsibilities include recruiting participants, ensuring protocol compliance, and analyzing data. Ideal candidates should have a Bachelor'...Hourly payFull time- ...Washington University in St. Louis is seeking a Clinical Research Coordinator I to support the Emergency Medicine department in coordinating clinical studies. The role involves managing study phases, recruiting participants, and ensuring protocol compliance in a busy ED...
$54.6k - $81.9k
...Hours 40 Position Summary Serve as a coordinator in The Life-space, isolation, and... .... Establishes excellent rapport with research participants, staff, and partners. Obtains... ...American Red Cross Work Experience: Clinical Research (2 Years) Skills: Not...Full timeFor contractorsWork experience placementWork at office- Washington University in St. Louis is seeking a Clinical Research Coordinator to screen and enroll patients for trials, coordinate collection of study requirements, and support the clinical teams through protocol follow-up. The CRC will manage multiple studies when needed...
- ObjectiveHealth is seeking a Clinical Research Coordinator I to support patient-focused clinical trials. You will identify, screen, enroll, and monitor patients under IRB-approved protocols and perform direct patient care activities including consent, blood draws, and ECGs...
- Washington University in St. Louis is seeking a Clinical Research Coordinator to oversee and coordinate complex clinical studies, ensure regulatory compliance, and support budget and billing processes. The role may supervise staff and serves as a resource to research teams...
- Washington University in St. Louis seeks a coordinator in the THuNDR Laboratory for postmortem brain research and coordination across AD and movement disorder studies... ...progress reports and manuscripts; this is a non-clinical #J-18808-Ljbffr Washington University in St....
- Washington University in St. Louis is seeking a Clinical Research Coordinator to screen and enroll patients in trials, coordinating collection of study requirements and supporting PI and clinical teams to ensure protocol compliance and patient safety on-site in St. Louis...
- Washington University in St. Louis is seeking a Research Coordinator to support the THRIVE study protocol. The role focuses on data collection... ...lies in a patient-care setting with regular desk work and clinical duties. Primary duties include coordinating all study phases...
$43.89k - $71.32k
Job Description - CLINICAL RESEARCH COORDINATOR I (T239171) CLINICAL RESEARCH COORDINATOR I - ( T239171 ) Description The University of Alabama at Birmingham (UAB), Pediatric Neurosurgery, is seeking a Clinical Research Coordinator I. The Clinical Research Coordinator...Remote workShift workDay shift- Washington University in St. Louis seeks a highly organized coordinator to refer and track research participant study visits for the Memory and Aging... ...investigators as a coordinator of a basic to moderately complex clinical research study; may manage multiple studies, acting as...
- Overview Velocity Clinical Research is an owned and integrated research site organization, providing excellence in patient care, high quality... ...an annual incentive program. Summary: The Clinical Research Coordinator II conducts and manages multiple clinical trials from start...Work at officeFlexible hours
- Mercy Research is seeking a Clinical Research Coordinator to manage day-to-day clinical trial operations, including patient recruitment, study coordination, data collection, and regulatory compliance. This onsite role collaborates with physicians, nurses, staff, and sponsors...
- Washington University in St. Louis seeks a Clinical Research Coordinator to support newborn NICU studies at Saint Louis Children’s Hospital. You will coordinate studies, manage regulatory requirements, and liaise with investigators, sponsors, and participants to ensure...
- Washington University in St. Louis is seeking a Clinical Research Coordinator for the Radiology Clinical Research Core (RadCore). The role supports multiple clinical studies, handling patient recruitment, data collection, and regulatory compliance in a hybrid, Monday-Friday...Monday to Friday
- ObjectiveHealth is seeking a Clinical Research Coordinator II to join our patient-focused team. This full-time role requires 3+ years of clinical research coordination experience and a passion for working directly with patients in IRB-approved trials. You will manage study...Full time
- Description Clinical Research Coordinator II Our clinical research company is looking to hire a qualified candidate for the full-time position of Clinical Research Coordinator II. The ideal candidate will possess 3+ years of clinical research coordination experience, and...Full timeTemporary workWork visaFlexible hours
- Washington University in St. Louis is seeking a Clinical Research Coordinator to assist investigators in coordinating basic to moderately complex clinical studies. The role involves managing protocol phases, participant recruitment, consent, data collection, and ensuring...
- ...Clinical Research Data CoordinatorAssists investigators as a data coordinator of numerous clinical research trials of all complexities, extracting data from the Electronic Medical Record (EMR) and other source documents and entering it into an Electronic Data Capture (...For contractorsWork experience placement
$64.3k - $99.7k
...Clinical Research CoordinatorOversees and coordinates complex or multi-site clinical research studies; serves as a resource to provide comprehensive information to clinical research staff by promoting a smooth operation, preparation of regulatory compliance and interaction...Work at office- ...ObjectiveHealth is hiring a Clinical Research Coordinator II in Missouri to support patient-focused trials. You will coordinate screenings, enroll patients, conduct clinic visits, collect data, and ensure regulatory compliance. This full-time role requires 3+ years...Full time
Do you want to receive more vacancies?
Subscribe and receive similar vacancies to Clinical Research Coordinator I - Pediatric Endocrinology. Be the first to apply!
- clinical research coordinator ii Saint Louis, MO
- clinical trials manager Saint Louis, MO
- neuroscience clinical research coordinator Saint Louis, MO
- clinical research coordinator no experience Saint Louis, MO
- clinical project manager Saint Louis, MO
- clinical research coordinator Saint Louis, MO
- clinical research part time Saint Louis, MO
- clinical research Saint Louis, MO
- clinical research manager remote Saint Louis, MO
- clinical research remote Saint Louis, MO


