Clinical Research Coordinator I (Data) - Medical Oncology
$49.2k - $73.8kWashington University in St. Louis
Scheduled Hours
40 Position Summary
Position assists investigators as a data coordinator of 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 (EDC).May be responsible for numerous research trials simultaneously. Helps ensure the accurate collection of study- required procedures while patients are receiving protocol treatment and are in active protocol follow-up; acts as liaison between the School, trial sponsors, vendors, and the study team. Responsible for helping the clinic coordinator and Principal Investigator (PI) manage and record data for all phases of study protocol as required by sponsoring agency to ensure compliance, patient safety and welfare, and data integrity. Job Description Primary Duties & Responsibilities:
Job Location/Working Conditions
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 Cross Work Experience:
No specific work experience is required for this position. Skills:
Not Applicable Driver's License:
A driver's license is not required for this position. More About This Job Required Qualifications
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, Database Management, Research Projects, Spreadsheet Analysis, Statistical Analysis Software (SAS) Grade
C09 Salary Range
$49,200.00 - $73,800.00 / Annually The 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. Questions For frequently asked questions about the application process, please refer to our External Applicant FAQ. Accommodation If 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 Screening
All 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 Statement Personal
For policies, detailed benefits, and eligibility, please visit: EEO Statement
Washington 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, 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.
40 Position Summary
Position assists investigators as a data coordinator of 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 (EDC).May be responsible for numerous research trials simultaneously. Helps ensure the accurate collection of study- required procedures while patients are receiving protocol treatment and are in active protocol follow-up; acts as liaison between the School, trial sponsors, vendors, and the study team. Responsible for helping the clinic coordinator and Principal Investigator (PI) manage and record data for all phases of study protocol as required by sponsoring agency to ensure compliance, patient safety and welfare, and data integrity. Job Description Primary Duties & Responsibilities:
- Manages patient-related data across all phases of clinical trials; ensures compliance with protocol guidelines and requirements of regulatory agencies; identifies procedural problems and/or inconsistencies.
- Monitors participant's progress throughout study, which includes documentation and reporting of adverse events; resolves protocol management issues and recommends corrective action as appropriate; serves as liaison between WU study team, the sponsor, and Clinical Research Organization (CRO)
- Extracts clinical data from EMR and receives clinical data from other source documents and enters it in a study specific electronic data capture system (EDC).
- Assures protocol compliance and adherence by performance of quality control checks of collected data
- Evaluates all lab and clinical assessments to ensure they are completed correctly and per protocol specification. Reviews collected clinical data in conjunction with PI or sub-investigator as appropriate
- Frequently communicates with sponsors and CROs, and responds to queries. Facilitates sponsor monitoring visits (if applicable).
- Attends patient-related, protocol, and educational meetings. May prepare oral or written presentations related to patient updates or protocol training. Attends sponsor monitoring meetings with the PI (if applicable). Performs other duties incidental to the work described herein
- Assists in developing plans for research projects and discusses 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.
- 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.
- 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 protocol management issues and recommends corrective action as appropriate; serves as liaison with funding or sponsoring agency.
- Evaluates and interprets collected clinical data as appropriate; prepares oral or written presentations or reports and analyses setting forth progress trends and provides recommendations or conclusions of the same.
- Performs other duties as assigned.
Job Location/Working Conditions
- Patient care setting.
- Typically sitting at desk or table.
- Office equipment.
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 Cross Work Experience:
No specific work experience is required for this position. Skills:
Not Applicable Driver's License:
A driver's license is not required for this position. More About This Job Required Qualifications
- Basic Life Support certification (Online Basic Life Support certifications, those without a skills assessment component, are not sufficient to meet the Basic Life Support requirements). Basic Life Support certification must be obtained within one month of hire date.
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, Database Management, Research Projects, Spreadsheet Analysis, Statistical Analysis Software (SAS) Grade
C09 Salary Range
$49,200.00 - $73,800.00 / Annually The 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. Questions For frequently asked questions about the application process, please refer to our External Applicant FAQ. Accommodation If 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 Screening
All 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 Statement Personal
- Up 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%.
- Wellness challenges, annual health screenings, mental health resources, mindfulness programs and courses, employee assistance program (EAP), financial resources, access to dietitians, and more!
- We 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: EEO Statement
Washington 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, 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.
Vacancy posted 14 hours ago
Similar jobs that could be interesting for youBased on the Clinical Research Coordinator I (Data) - Medical Oncology in Saint Louis, MO vacancy
- ## Clinical Research Coordinator III - Pediatrics Hematology & OncologyApplyremote type... ...: Washington University Medical Campustime type: Full timeposted... ...with Hematology/Oncology and other divisions and departments... ...research study/projects, data collection, and the management...DataMedicalWork experience placementWork at office
- ...Assists in developing plans for research projects and discusses the... ...study design as appropriate.* Coordinates the development of forms,... ...manuals for study progress, data collection and coding; reviews... ...Evaluates and interprets collected clinical data as appropriate; prepares...DataMedicalTraineeshipRemote work
- Scheduled Hours40Position SummaryOversees and coordinates complex or multi-site clinical research studies; serves as a resource to provide comprehensive information... ...instructional procedure manuals for study progress, data collection and coding; reviews journals, abstracts...DataMedicalWork experience placementWork at office
$47.4k - $71.2k
Position Summary Position assists investigators as a data coordinator of 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 (EDC). May be responsible...DataMedicalWork experience placementWork at office- ...Clinical Research Coordinator I Our clinical research company is looking to hire... ...assessments, blood draws, medication administration, ECG, etc.... ...attention to detail for clean data entry, regulatory... ...Urology, Dermatology, and/or Oncology What Success Looks Like...DataFull timeTemporary workWork visaFlexible hours
- ...Registered Nurse - Clinic It's more than a career, it's a calling MO... ...PRIMARY RESPONSIBILITIES Coordinates clinical studies in the medical research area. Develops an understanding... ...Completes or oversees completion of data entry in a timely manner. Ensures...DataMedicalHourly payMonday to FridayFlexible hoursShift workDay shift
$58k - $62k
...our neurology practice in a role as a Clinical Research Coordinator. This unique role offers the... ...recruitment, regulatory documentation, and data entry, while also performing essential... ...assist with the daily activities of a medical office, including rooming patients, preparing...DataMedicalFull timePart timeWork at office- ## Clinical Research Coordinator I (Part Time) - Pediatrics Adolescent MedicineApplyremote type: On Campus... ...: Washington University Medical Campustime type: Part timeposted on:... ...records* Project infrastructure and data management + Assists with compliance...DataMedicalFull timePart timeWork experience placementWork at office
$60k - $90k
...for all. With hundreds of research locations, mobile clinics, and clinicians across the... ...need, and contribute to the medical breakthroughs of tomorrow.... ...The Clinical Research Coordinator’s primary responsibilities... ...Documentation Record data legibly and enter in real...DataMedicalFull timeTemporary workWork at officeLocal areaWorldwideVisa sponsorshipWork visaRelocation packageFlexible hours- ...At Headlands Research, we are dedicated to enhancing clinical trial delivery within our communities... .... Clinical Research Coordinator (CRC) We’re seeking a Clinical... ...: Health insurance (medical, dental, vision), HSA, FSA... ...Ensure timely data entry and resolution of...DataMedicalFull timeWork at officeLocal areaRemote workMonday to Friday
- ## Clinical Research Coordinator III - NeurologyApplyremote type: On Campus/Onsitelocations: Washington University Medical Campustime type: Full timeposted on: Posted Todayjob requisition id:... ...and reporting of clinical research data, and may include staff training and...DataMedicalWork experience placementWork at office
- A leading research university in St. Louis seeks a candidate to assist in research project development, manage clinical studies, and analyze data. Candidates should possess strong analytical skills and a Bachelor’s degree in a relevant field. The position offers generous...Data
$47.4k - $71.2k
Washington University in St. Louis is seeking a Data Coordinator to assist in clinical research trials. The role involves extracting data from the Electronic Medical Records and ensuring accurate study procedure collection. Candidates should possess a Bachelor's degree,...DataMedical$47.4k - $71.2k
...Job Title Data Coordinator for Clinical Research Trials Position Summary Assists investigators as a data coordinator of clinical research trials... ...all complexities, extracting data from the Electronic Medical Record (EMR) and other source documents and entering it...DataMedicalWork experience placementWork at office$47.4k - $71.2k
...our dynamic, mission-driven team as a Clinical Research Coordinator I, where you will assist... ...simultaneously, acting as an liaison with the Medical School, sponsoring agencies, the community... ...and interprets collected clinical data as appropriate; prepares oral or written...DataMedicalWork experience placementWork at office- ## Clinical Research Coordinator IV - CardiologyApplyremote type: On Campus/Onsitelocations: Washington University Medical Campustime type: Full timeposted on: Posted Todayjob requisition id:... ...Prepares study progress reports and data safety monitoring reports for PI and...DataMedicalWork experience placementWork at office
$52.6k - $78.9k
Position Summary The Clinical Research Coordinator II (CRC II) will manage all phases of clinical research... ...support to fellows, residents, medical students, and research scholars. As a... ...procedure manuals for study progress, data collection and coding; reviews journals...DataMedicalWork experience placementWork at office- ...professional nursing care to patients within the medical practice in support of, and as directed... ...of patients and completes related clinical paperwork. The incumbent in this position... ...to access information and enter clinical data. Equipment Used : Must be able to operate...DataMedicalFull timeLocal area
$75.2k - $128.8k
Washington University is seeking a clinical research coordinator in St. Louis, Missouri, to lead oncology radiopharmaceutical trials. The candidate will be responsible... ...overseeing protocol compliance, and ensuring quality data collection. Applicants must possess a Bachelor’s...Data- ...environment and established clinic with experienced,... ...cases annually (2024 data) Most patients receive integrated medical oncology and/or radiation oncology... ...planning and coordination Academic & Educational... ...conferences, or clinical research Engagement in...DataMedicalTraineeshipWork at office
- .... At Houston Methodist, the Medical Laboratory Scientist position... ...Certified as a Medical Technologist, Clinical Laboratory Scientist, Medical... ...patient care information and data in a comprehensive manner.... ...neurology and neurosurgery, oncology, and primary and general...DataMedicalReliefWork at officeShift work
$75.2k - $128.8k
Clinical Research Project Manager - Infectious Diseases Washington University... ...meetings, facilitate coordination across teams, and help ensure... ...subcontracts (biomarkers, imaging, data management) which includes... ...Escalate issues relevant to medical personnel as appropriate for...DataMedicalWork experience placementFor subcontractorWork at officeLocal areaFlexible hours- A leading research university in St. Louis seeks a Data Coordinator to assist in clinical trials. This role involves managing patient-related data, ensuring compliance with protocols, and extracting data from medical records. The position requires a Bachelor’s degree and...DataMedical
$52.6k - $78.9k
...A leading university in Missouri seeks a research coordinator to assist in complex clinical studies. The role involves developing study plans, ensuring protocol compliance, and evaluating data. Candidates should have a Bachelor's degree and at least 2 years of clinical...Data$47.4k - $71.2k
...A leading research university in St. Louis seeks a Clinical Research Coordinator for industry-sponsored trials, supporting MS patients. Responsibilities include managing... ...participants, and evaluating clinical data. Candidates should have a bachelor’s degree and...Data- ...Houston Methodist is seeking a Research Coordinator III in St. Louis, Missouri. This role involves coordinating clinical research projects, managing patient data, and providing administrative support. The ideal candidate will have at least five years of clinical research...Data
- ...Washington University in St. Louis is hiring a Clinical Research Coordinator I (Part Time) for its Pediatrics Adolescent Medicine team. The position... ...regulatory compliance, managing project budgets, and data management. Candidates should have a Bachelor's degree and...DataPart time
$52.6k - $78.9k
...join a well-established, collaborative clinical research team in the Division of Pulmonary and Critical... .... Additional responsibilities include coordinating study activities, maintaining... ...procedure manuals for study progress, data collection and coding; reviews journals...DataWork experience placementWork at office$47.4k - $71.2k
...Overview The clinical research coordinator’s position focuses on industry-sponsored clinical trials at the John L. Trotter Multiple Sclerosis Center... ..., and treatments); evaluates and interprets clinical data; prepares presentations or reports on progress trends and...DataWork experience placementWork at office$56.2k - $87.1k
...treatment, precision medicine, and research opportunities to pediatric... ...have access to leading‑edge clinical trials which focus on... ...Description As a Clinical Research Coordinator, you will work alongside our... ...reporting of clinical research data, and may include staff...DataWork experience placementWork at office
Do you want to receive more vacancies?
Subscribe and receive similar vacancies to Clinical Research Coordinator I (Data) - Medical Oncology. Be the first to apply!
Related searches
- clinical research coordinator Saint Louis, MO
- neuroscience clinical research coordinator Saint Louis, MO
- clinical research coordinator ii Saint Louis, MO
- clinical research coordinator no experience Saint Louis, MO
- clinical project manager Saint Louis, MO
- clinical trials manager Saint Louis, MO
- clinical data coordinator Saint Louis, MO
- clinical coordinator registered nurse Saint Louis, MO
- clinical nurse coordinator Saint Louis, MO
- medical coordinator Saint Louis, MO

