186 Results for

Research Jobs in Wildwood, IL

Jobs

Saint Louis, MO

li>Multidisciplinary Clinic Model: ALS Patients receive comprehensive care from a team including a dietician, speech therapist, PT/OT, social worker, and the clinic directorall in a single 4-hour visit.

SLUCare Physician Group and SSM Health have partnered for decades to provide exceptional medical services to patients at Cardinal Glennon Children‘s Hospital, St. Mary‘s Hospital, and most recently Saint Louis University Hospital.

2 days ago

Saint Louis, MO

p>The program is deeply committed to Clinical Interventional Radiology, pioneering a true clinic-based patient-centered model with longitudinal patient care, ensuring that IR remains at the heart of disease management, leading to better outcomes and long-term patient relationships.

A pioneering Vascular & Interventional Radiology Program at SSM Health Saint Louis University Hospital (SLU) is seeking a board-eligible or board-certified, clinical minded, forward-thinking, Vascular and Interventional Radiologist to join our vascular-focused IR practice with a well-developed interventional oncology program.

2 days ago

Chesterfield, MO

p>This general interest posting is designed for Clinical Research Assistants (RAs) who may not see a current opening that aligns with their location, but want to be considered for future opportunities across our growing network of clinical research sites nationwide.

We welcome interest from candidates who bring:

A bachelor's or master's degree involving 1+ year of laboratory classes, preferably within a scientific or healthcare-related field (e.g., biology, chemistry, psychology, pre-med, or similar) and/or.

30+ days ago

Chesterfield, MO

p>The Role:

As a Clinical Research Assistant, you'll work side-by-side with experienced Clinical Research Coordinators, Investigators, and cross-functional teams to support all aspects of clinical trial execution-from subject screening, data entry, to patient recruitment. As a leading network of advanced clinical trial sites, we leverage cutting-edge technology and exceptional support services to broaden outreach and participation.

30+ days ago

Chesterfield, Missouri

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Headlands Research will never ask a candidate for personal identifiable information (date of birth, social security number, driver’s license information, etc) via email or messenger tools, or for a financial deposit of any kind.

17 days ago

Crystal City, MO
strong>Candidates with current Phlebotomy certification or Medical Assistant (MA) certification are strongly preferred, as this role may include specimen collection and basic clinical procedures. The CRC will coordinate and support all aspects of clinical trials and research studies, including subject recruitment, data collection, regulatory compliance, and specimen handling.
30+ days ago

Chesterfield, MO
p>Qualifications:
Minimum of two years of experience as a licensed physician assistant, family or non-acute adult nurse practitioner treating a wide variety of therapeutic areas for the adult and geriatric patient population required (internal medicine, family medicine, urgent care, emergency medicine). The site's team brings more than 20 years of experience, including many highly accomplished principal investigators across multiple therapeutic areas that are helping to improve lives through advancement of new drug therapies and medical devices.
30+ days ago

Chesterfield, Missouri
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17 days ago

Chesterfield, MO
p>Qualifications:
Minimum of two years of experience as a licensed family or non-acute adult nurse practitioner or physician assistant treating a wide variety of therapeutic areas for the adult and geriatric patient population required (internal medicine, family medicine, urgent care, emergency medicine). The site's team brings more than 20 years of experience, including many highly accomplished principal investigators across multiple therapeutic areas that are helping to improve lives through advancement of new drug therapies and medical devices.
30+ days ago

Creve Coeur, MO
The Clinical Research Nurse is responsible for the day-to-day operational tasks related to clinical trials and performs a variety of duties including, but not limited to, volunteer recruitment, drug/device/supply inventory maintenance, interaction with physicians, nurses, office staff, patients, and clinical monitors.
From day one, Mercy offers outstanding benefits - including medical, dental, and vision coverage, paid time off, tuition support, and matched retirement plans for team members working 32+ hours per pay period.
30+ days ago

Chesterfield, Missouri
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17 days ago

St. Louis, MO
$19.21–$28.85 / hour
Collects data from study participants, medical records, interviews, questionnaires, diagnostic tests and other sources; • Performs basic evaluation and interpretation of collected data and prepares appropriate reports and documentation as necessary; • Prepares and distributes study packets and information. • Performs basic/scripted assessments to confirm eligibility to participate in study; • Explains and schedules laboratory and diagnostic procedures and/or treatment as required in the study; • Refers participants to basic resources as necessary.
30+ days ago

Chesterfield, MO
As a leading network of advanced clinical trial sites, we leverage cutting-edge technology and exceptional support services to broaden outreach and participation. Join a leading, integrated clinical research network dedicated to high-quality data, patient-centered care, and innovation in clinical trials.
16 days ago

Ballwin, MO
The Clinical Research Nurse is responsible for the day-to-day operational tasks related to clinical trials and performs a variety of duties including, but not limited to, volunteer recruitment, drug/device/supply inventory maintenance, interaction with physicians, nurses, office staff, patients, and clinical monitors.
From day one, Mercy offers outstanding benefits - including medical, dental, and vision coverage, paid time off, tuition support, and matched retirement plans for team members working 32+ hours per pay period.
30+ days ago

St. Louis, MO
$50–$55 / hour
With interest/expertise in Science 37's decentralized model of care delivery, the Mobile Research Nurse will perform delivery of care to participants as well as collaborate with brick and mortar sites, if indicated, for shared clinical trial implementation.
Science 37's Nursing Solutions Group brings together expert nurses who share a passion for organizing, planning and implementing mobile clinical nurse services to participants in clinical trials.
12 days ago

St. Louis, MO
$17.34–$25.40 / hour
Primary Duties & Responsibilities: Maintains and updates site demographics on computer database; logs forms received and file as appropriate; prepares reports from database to include weekly reports and other reports as requested. Receives and disseminates study-related regulatory documents and correspondence; assists in screening documents for completeness and compliance with protocol and appropriate regulations; assists in investigating incomplete, inaccurate or missing documents to ensure accuracy and completeness of data.
30+ days ago

Chesterfield, MO
$45,000–$100,000 / year
p>This general interest posting is designed for experienced Clinical Research Coordinators (CRCs) who may not see a current opening that aligns with their location, but want to be considered for future opportunities across our growing network of clinical research sites nationwide. They play a hands-on role in advancing new therapies, supporting patients through clinical trials, and ensuring studies are conducted with the highest level of quality and care.
30+ days ago

Chesterfield, Missouri
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15 days ago

St. Louis, MO
$19.21–$28.85 / hour
p>• Collects data from study participants, medical records, interviews, questionnaires, diagnostic tests and other sources; performs basic evaluation and interpretation of collected data and prepares appropriate reports and documentation as necessary; prepares and distributes study packets and information.
Primary Duties & Responsibilities:
• Participates in the recruitment of study participants as identified in related protocol; • Visits with study participants to explain study, obtains informed consent of participants, and completes screening procedures per protocol.
30+ days ago

St. Louis, MO
$19.21–$28.85 / hour
p>• Collects data from study participants, medical records, interviews, questionnaires, diagnostic tests and other sources; performs basic evaluation and interpretation of collected data and prepares appropriate reports and documentation as necessary; prepares and distributes study packets and information.
• Performs basic/scripted assessments to confirm eligibility to participate in study; explains and schedules laboratory and diagnostic procedures and/or treatment as required in the study; refers participants to basic resources as necessary.
30+ days ago

New
St. Louis, MO
$19.21–$28.85 / hour
li>Collects data from study participants, medical records, interviews, questionnaires, diagnostic tests and other sources; performs basic evaluation and interpretation of collected data and prepares appropriate reports and documentation as necessary; prepares and distributes study packets and information.
Performs basic/scripted assessments to confirm eligibility to participate in study; explains and schedules laboratory and diagnostic procedures and/or treatment as required in the study; refers participants to basic resources as necessary.
3 days ago

New
St. Louis, MO
$60,000–$90,000 / year
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The expected salary range for this role is $60,000 - $90,000 USD per year for full time team members.
With programs like Future of Medicine, which makes advanced health screenings and research opportunities accessible to communities worldwide, and Difference Makers, which supports local leaders to expand their community health and wellbeing efforts, we put people at the heart of medical progress.
3 days ago

St. Louis, MO
$56,200–$87,100 / year
li>
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; consents participants for non-therapeutic clinical trials and performs blood draws and other specimen collection as needed.
Skills:
Clinical Research Management, Clinical Study Protocols, Database Management, Data Entry, Detail-Oriented, Freezerworks (Software), Ordering Supplies, Organizing, Participant Recruiting, Research Projects, Spreadsheet Analysis, Statistical Analysis Software (SAS), Team Supervision, Written Communication.
30+ days ago

MO
ul>
Reviews clinical trial protocols to determine if each new study is a qualified clinical trial pursuant to CMS policy; creates a detailed Coverage Analysis using clinical trial documents to designate which procedures/services may be "routine care" and billable to patient insurance and which should be billed to the study sponsor based on relevant regulations and determinations; serves as National and Local Coverage Determination (NCD and LCD) subject matter expert; interfaces with study teams and sponsors to resolve discrepancies in specific protocol assessments; interfaces with study teams and principal investigators to assist with coverage analysis determinations; performs document review for alignment for each study.
Acts as liaison with partnering hospital to ensure each new study is built in the electronic medical record (EMR) system; submits build forms, maintains spreadsheet of builds, requests updates / corrections.
30+ days ago

St. Louis, MO
li>Not easily distracted: You have the ability to stay focused while running different protocols, resolving and submitting IRB responses and audit findings, tracking AE and SAE events, and maintaining eSource material for assigned studies.
ObjectiveHealth is a clinical research company that uses proprietary technology to:
Increase patient access to research trials within our communities,
Provide physicians with enhanced care options for current patients, and.
16 days ago

St. Louis, MO
$56,200–$87,100 / year
Serves as responsible for 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. Designs, implements and manages all phases of study/protocol; ensures compliance with protocol guidelines and requirements of regulatory agencies; identifies problems and/or inconsistencies and monitors participant's progress to include documentation and reporting of adverse events; resolves IRB/protocol management issues and recommends corrective action as appropriate; serves as liaison with funding or sponsoring agency.
30+ days ago

MO
Remote
$17.10–$29.09 / hour
p>As a Research Assistant with the Light Institute for Global Health and Transformation, you will gain hands-on experience across implementation science research, public health clinical trials, and the day-to-day operations that keep high-impact projects moving. 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.
11 days ago

St. Louis, MO
$17.10–$29.09 / hour
As a Research Assistant with the Light Institute for Global Health and Transformation, you will gain hands-on experience across implementation science research, public health clinical trials, and the day-to-day operations that keep high-impact projects moving. 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.
22 days ago

St. Louis, MO
$16.92–$26.44 / hour
li>
Communicate daily with the other members of the lab (graduate students, post-docs, and undergraduate research assistants) to coordinate scheduling and train and work with undergraduates on various aspects of the project. 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.
30+ days ago

St. Louis, MO
$19.21–$28.85 / hour
li>Collects data from study participants, medical records, interviews, questionnaires, diagnostic tests and other sources; performs basic evaluation and interpretation of collected data and prepares appropriate reports and documentation as necessary; prepares and distributes study packets and information. This position will also be responsible in data analyses ranging from basic data quality control to more advanced spatial and temporal analyses of HD-DOT data, to relating variance in this data with concurrent physiological metrics we well as short- and long-term outcomes.
19 days ago

Saint Charles, Missouri
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The research assistant is responsible for assisting designated University personnel with daily activities related to research assignments, scholarly publication, geospatial curriculum testing, and educational and community outreach projects as they pertain to the assignment and/or grant specifications. Please click here to view Lindenwood University’s flexible work designation descriptions.
30+ days ago

St. Louis, MO
$93,300–$167,800 / year
Primary Duties & Responsibilities: Provides direct patient care to include obtaining patient history, performing patient assessment via observation, interview and examination; orders, performs and interprets diagnostic studies; performs preventative health assessments, screenings, immunizations and care; provides direct treatment and management of acute and chronic disease conditions; develops and implements patient-centered plan of care in collaboration with physicians, patients, consultants, nurses, ancillary care providers and others as appropriate to the patient's condition. Certifications/Professional Licenses: Advanced Practice Nurse (APN) - Illinois Department of Financial and Professional Regulation, Advanced Practice Nurse (APN) - Missouri Division of Professional Registration, Certified Nurse Practitioner - Illinois Department of Financial and Professional Regulation, Certified Nurse Practitioner - Missouri Division of Professional Registration, Physician Assistant - Illinois Department of Financial and Professional Regulation, Physician Assistant - Missouri Division of Professional Registration.
22 days ago

St. Louis, MO
$62,000–$96,100 / year
li>Serves as responsible for 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.
Designs, implements and manages all phases of study/protocol; ensures compliance with protocol guidelines and requirements of regulatory agencies; identifies problems and/or inconsistencies and monitors participant's progress to include documentation and reporting of adverse events; resolves IRB/protocol management issues and recommends corrective action as appropriate; serves as liaison with funding or sponsoring agency.
30+ days ago

St. Louis, MO
$52,600–$78,900 / year
p>Primary Duties & Responsibilities:
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.
The WashU Medicine Center for Pediatric Neuromuscular Disorders (https://pediatricneuromusculardisorders.wustl.edu/) provides quality care, state-of-the-art treatment, precision medicine, and research opportunities to pediatric and young adult patients diagnosed with neuromuscular disorders.
30+ days ago

Chesterfield, MO
The culture emphasizes strong training and development, high visibility project work, collaboration with internal teams and external research partners, and opportunities to gain significant experience in product development, formulation, and enzyme analytics. You will receive hands-on training over approximately 2-3 weeks to qualify on the assay, working directly with a trainer, shadowing procedures, performing assays under supervision, and demonstrating the ability to replicate results independently.
15 days ago

MO
Remote
$52,600–$78,900 / year
Position assists investigators as coordinator of a complex clinical research study; 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 Job Description Primary Duties & Responsibilities: 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. 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.

30+ days ago

St. Louis, MO
$56,200–$96,100 / year
p>Basic Life Support - American Heart Association, Basic Life Support - American Red Cross, Registered Nurse - Illinois Department of Financial and Professional Regulation, Registered Nurse - Missouri Division of Professional Registration. 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.
24 days ago

St. Louis, MO
$47,400–$71,200 / year
p>Primary Duties & Responsibilities:
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 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 funding or sponsoring agency.
Recruits and enrolls study participants; makes and/or participates in making determinations of eligibility based on diagnostic criteria and/or observations/analysis in participant interviews; develops informed consent packets for study participants and confers with participants to explain purpose of study and obtain completed informed consent packets; explains diagnostic procedures and treatment plans to address participant/family concerns; administers/scores tests and/or evaluates all lab and clinical assessments to ensure they are completed in a timely manner.
30+ days ago

St. Louis, MO
$47,400–$71,200 / year
p>• 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 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 funding or sponsoring agency.
• Recruits and enrolls study participants • Makes and/or participates in making determinations of eligibility based on diagnostic criteria and/or observations/analysis in participant interviews • Develops informed consent packets for study participants and confers with participants to explain purpose of study and obtain completed informed consent packets • Explains diagnostic procedures and treatment plans to address participant/family concerns • Administers/scores tests and/or evaluates all lab and clinical assessments to ensure they are completed in a timely manner.
30+ days ago

St. Louis, MO
$52,600–$78,900 / year
li>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.
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.
30+ days ago

MO
li>
Identifies all adverse events (AEs) and determines whether or not they are reportable; collaborates with the PI to determine AE attributes, including relatedness to study; conducts and documents consent for participants for all types of studies, including those that are complex in nature and/or require clinical research orders in EHR.
Maintains participant-level documentation for all studies, including those that are complex in nature, require access to the EHR or require SLUCare/SSM charge routing; screens participants for complex studies (e.g., procedural, and interventional studies).
30+ days ago

St. Louis, MO
$52,600–$78,900 / year
li>
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.
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.
30+ days ago

New
St. Louis, MO
$52,600–$78,900 / year
li>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.
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.
5 days ago

MO
p>Under the direction of the Principal Investigator or designee, the Clinical Research Nurse I is responsible to carry out all delegated tasks related to complex protocols testing investigational drugs, devices, or research interventions.
Maintains participant-level documentation for all studies, including those that are complex in nature, require access to the EHR or require SLUCare/SSM charge routing.
30+ days ago

St. Louis, MO
$47,400–$71,200 / year
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.
If you are unable to use our online application system and would like an accommodation, please email CandidateQuestions@wustl.edu or call the dedicated accommodation inquiry number at 314-935-1149 and leave a voicemail with the nature of your request.
30+ days ago

Chesterfield, MO
We are proud to be an Engineering News-Record (ENR) Top 500 Design Firm for our engineering design services and a ClearlyRated Best of Staffing winner for both client and talent service.
If you would like to request a reasonable accommodation, such as the modification or adjustment of the job application process or interviewing process due to a disability, please email actalentaccommodation@actalentservices.com for other accommodation options.
8 days ago

New
Chesterfield, MO
We are proud to be an Engineering News-Record (ENR) Top 500 Design Firm for our engineering design services and a ClearlyRated Best of Staffing winner for both client and talent service.
If you would like to request a reasonable accommodation, such as the modification or adjustment of the job application process or interviewing process due to a disability, please email actalentaccommodation@actalentservices.com for other accommodation options.
1 day ago

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Research Jobs in Wildwood, IL

Academic Neuromuscular Neurologist - Research, Mentor, and Make an Impact - SLUCare - St. Louis, MO SSM Health

Assistant/Associate Professor - Join a Growing Clinical IR Team in a Unique Academic-Private Program SSM Health

Clinical Research Assistant Opportunities - Multiple Locations Nationwide Headlands Research Inc

Research Assistant / Patient Recruitment Headlands Research Inc

Research Assistant / Patient Recruitment Headlands Research

Clinical Research Coordinator ECN Operating LLC

Physician Assistant - Clinical Research Headlands Research Inc

Physician Assistant - Clinical Research Headlands Research

Nurse Practitioner - Clinical Research Headlands Research Inc

Clinical Research Nurse - Pratt Cancer Center Mercy

Nurse Practitioner - Clinical Research Headlands Research

Clinical Research Study Assistant II - Neurology Washington University in St Louis

Clinical Research Coordinator Headlands Research Inc

Clinical Research Nurse - Mercy Clayton/Clarkson Oncology Clinic Mercy

Per Diem Clinical Research Nurse - Home Visits Science 37

Clinical Research Study Assistant I (Hybrid) - Radiology Washington University in St Louis

Clinical Research Coordinator I/II/III Opportunities - Multiple Locations Nationwide Headlands Research Inc

Clinical Research Coordinator Headlands Research

Clinical Research Study Assistant II (PRN) - Cardiology Washington University in St Louis

Clinical Research Study Assistant II - Emergency Medicine Washington University in St Louis

Clinical Research Study Assistant II - Obstetrics and Gynecology Washington University in St Louis

Clinical Research Coordinator II Care Access

Per Diem Clinical Research Nurse - Home Visits Science 37 Inc

Clinical Research Coordinator III - Psychiatry Washington University in St Louis

Clinical Research Coverage Analyst Saint Louis University

Clinical Research Coordinator I ObjectiveHealth Inc

Clinical Research Coordinator III - Pediatrics Genetics Washington University in St Louis

Research Assistant (Part-time/Remote) - Infectious Diseases Washington University in St Louis

Research Assistant (PRN/Remote) - Infectious Diseases Washington University in St Louis

Research Assistant (PRN) - Infectious Diseases Washington University in St Louis

Research Assistant (Part-time) - Infectious Diseases Washington University in St Louis

Research Technician II - Social Science Washington University in St Louis

Clinical Research Study Assistant II - Radiology Washington University in St Louis

GIS Research Assistants Summer 2026 Lindenwood University

Research Nurse Practitioner or Physician Assistant - Oncology Washington University in St Louis

Senior Clinical Research Coordinator - Medical Oncology Washington University in St Louis

Clinical Research Coordinator II - Neurology Washington University in St Louis

Biochemistry Research Assistant Actalent Inc

Clinical Research Coordinator II (Regulatory/Remote) - Medical Oncology Washington University in St Louis

Research Nurse Coordinator I (Budget Coordinator) (Hybrid) - Center for Clinical Studies Washington University in St Louis

Clinical Research Coordinator I - Obstetrics and Gynecology Washington University in St Louis

Clinical Research Coordinator I (Hybrid) - Neurology Washington University in St Louis

Clinical Research Coordinator II - Pulmonary & Critical Care Medicine Washington University in St Louis

Clinical Research Nurse - Internal Medicine Saint Louis University

Clinical Research Coordinator II - Neurosurgery Washington University in St Louis

Clinical Research Coordinator II - Orthopedic Surgery Washington University in St Louis

Clinical Research Nurse Saint Louis University

Clinical Research Coordinator I - Neurology Washington University in St Louis

**Biochemistry Research Assistant** Actalent Inc

**Biochemistry Research Assistant** 25/HR Actalent Inc

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