Clinical Research Coordinator
$35 - $42/hr
Clinical Research Coordinator - Jefferson City, MO Work Set-Up: On-site Schedule Weekly Hours: 24 ... Proficiency with EDC systems , data entry accuracy, and query management. Please note: This ...
$35 - $42/hr
Clinical Research Coordinator - Jefferson City, MO Work Set-Up: On-site Schedule Weekly Hours: 24 ... Proficiency with EDC systems , data entry accuracy, and query management. Please note: This ...
$35 - $42/hr
Clinical Research Coordinator - Jefferson City, MO Work Set-Up: On-site Schedule Weekly Hours: 24 ... Proficiency with EDC systems , data entry accuracy, and query management. Please note: This ...
Saint Louis, MO · On-site
$75 - $129/hr
## Manager Division Clinical Research - Radiation OncologyApplyremote type: On Campus/Onsitelocations: Washington University Medical Campustime type: Full timeposted on: Posted Yesterdayjob requisition ...
Saint Louis, MO · On-site
$75 - $129/hr
## Manager Division Clinical Research - Radiation OncologyApplyremote type: On Campus/Onsitelocations: Washington University Medical Campustime type: Full timeposted on: Posted Yesterdayjob requisition ...
Leadership of the Functional Research Groups: * Makes hiring and staffing decisions in the ... Skills: Clinical Project Management, Clinical Systems, Clinical Trials Administration, Deadline ...
Leadership of the Functional Research Groups: * Makes hiring and staffing decisions in the ... Skills: Clinical Project Management, Clinical Systems, Clinical Trials Administration, Deadline ...
Saint Louis, MO · On-site
$58K - $90K/yr
... clinical research staff Primary Duties & Responsibilities ... Manages protocol study start up and study launch, submission, and maintenance of essential ...
Saint Louis, MO · On-site
$58K - $90K/yr
... clinical research staff Primary Duties & Responsibilities ... Manages protocol study start up and study launch, submission, and maintenance of essential ...
$58K - $90K/yr
... clinical research staff Primary Duties & Responsibilities ... Manages protocol study start up and study launch, submission, and maintenance of essential ...
$58K - $90K/yr
... clinical research staff Primary Duties & Responsibilities ... Manages protocol study start up and study launch, submission, and maintenance of essential ...
Position Overview - Clinical Research Associate As a CRA, you'll manage clinical study activities across multiple sites within one or more projects, with a focus on medical devices. You will oversee ...
Position Overview - Clinical Research Associate As a CRA, you'll manage clinical study activities across multiple sites within one or more projects, with a focus on medical devices. You will oversee ...
$75K - $128K/yr
Responsible for the management of the Division of Clinical Research and the day-to-day functions of the division. * Responsible for recruiting, hiring, managing and review of clinical research staff ...
$75K - $128K/yr
Responsible for the management of the Division of Clinical Research and the day-to-day functions of the division. * Responsible for recruiting, hiring, managing and review of clinical research staff ...
$24 - $32/hr
You may need to work a little earlier/later as needed JOB SUMMARY The Clinical Research Coordinator provides clinical research support for studies involving human subjects and manages the daily ...
$24 - $32/hr
You may need to work a little earlier/later as needed JOB SUMMARY The Clinical Research Coordinator provides clinical research support for studies involving human subjects and manages the daily ...
Saint Louis, MO · On-site
$75K - $128K/yr
Responsible for the management of the Division of Clinical Research and the day-to-day functions of the division. * Responsible for recruiting, hiring, managing and review of clinical research staff ...
Saint Louis, MO · On-site
$75K - $128K/yr
Responsible for the management of the Division of Clinical Research and the day-to-day functions of the division. * Responsible for recruiting, hiring, managing and review of clinical research staff ...
Des Peres, MO · On-site
$24 - $32/hr
You may need to work a little earlier/later as needed JOB SUMMARY The Clinical Research Coordinator provides clinical research support for studies involving human subjects and manages the daily ...
Des Peres, MO · On-site
$24 - $32/hr
You may need to work a little earlier/later as needed JOB SUMMARY The Clinical Research Coordinator provides clinical research support for studies involving human subjects and manages the daily ...
Des Peres, MO · On-site
$24 - $32/hr
You may need to work a little earlier/later as needed JOB SUMMARY The Clinical Research Coordinator provides clinical research support for studies involving human subjects and manages the daily ...
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Des Peres, MO · On-site
$24 - $32/hr
You may need to work a little earlier/later as needed JOB SUMMARY The Clinical Research Coordinator provides clinical research support for studies involving human subjects and manages the daily ...
Des Peres, MO · On-site
$24 - $32/hr
You may need to work a little earlier/later as needed JOB SUMMARY The Clinical Research Coordinator provides clinical research support for studies involving human subjects and manages the daily ...
Des Peres, MO · On-site
$24 - $32/hr
You may need to work a little earlier/later as needed JOB SUMMARY The Clinical Research Coordinator provides clinical research support for studies involving human subjects and manages the daily ...
$24 - $32/hr
You may need to work a little earlier/later as needed JOB SUMMARY The Clinical Research Coordinator provides clinical research support for studies involving human subjects and manages the daily ...
$24 - $32/hr
You may need to work a little earlier/later as needed JOB SUMMARY The Clinical Research Coordinator provides clinical research support for studies involving human subjects and manages the daily ...
Des Peres, MO · On-site
$22.75 - $30.25/hr
You may need to work a little earlier/later as needed JOB SUMMARY The Clinical Research Coordinator provides clinical research support for studies involving human subjects and manages the daily ...
Des Peres, MO · On-site
$22.75 - $30.25/hr
You may need to work a little earlier/later as needed JOB SUMMARY The Clinical Research Coordinator provides clinical research support for studies involving human subjects and manages the daily ...
Saint Louis, MO · On-site
$22.75 - $30.25/hr
Implements and manages all phases of study/protocol; ensures compliance with protocol guidelines ... Collects clinical data under clinical research protocols. Minimum Requirements Education * Bachelor ...
Saint Louis, MO · On-site
$22.75 - $30.25/hr
Implements and manages all phases of study/protocol; ensures compliance with protocol guidelines ... Collects clinical data under clinical research protocols. Minimum Requirements Education * Bachelor ...
Edina, MO · On-site
$21.25 - $28.25/hr
Experience in managing confidential information and/or issues using discretion and Judgment * Certified Clinical Research Coordinator (SOCRA or ACRP) - preferred DaVita Clinical Research (DCR), a ...
Edina, MO · On-site
$21.25 - $28.25/hr
Experience in managing confidential information and/or issues using discretion and Judgment * Certified Clinical Research Coordinator (SOCRA or ACRP) - preferred DaVita Clinical Research (DCR), a ...
Data Capture Management * Staff Training/Research Education * Financials/Fiscal Management ... One of the following: Certified Clinical Research Coordinator, Certified Clinical Research ...
Data Capture Management * Staff Training/Research Education * Financials/Fiscal Management ... One of the following: Certified Clinical Research Coordinator, Certified Clinical Research ...
Saint Louis, MO · On-site
$21.58 - $35.84/hr
... Clinical Research Coordinator. This is a patient facing role that will work with patients ... Implements and manages all phases of study/protocol; ensures compliance with protocol guidelines ...
Saint Louis, MO · On-site
$21.58 - $35.84/hr
... Clinical Research Coordinator. This is a patient facing role that will work with patients ... Implements and manages all phases of study/protocol; ensures compliance with protocol guidelines ...
Data Capture Management * Staff Training/Research Education * Financials/Fiscal Management ... One of the following: Certified Clinical Research Coordinator, Certified Clinical Research ...
Data Capture Management * Staff Training/Research Education * Financials/Fiscal Management ... One of the following: Certified Clinical Research Coordinator, Certified Clinical Research ...
Kansas City, MO · On-site
$67K - $84K/yr
The Clinical Nurse Research Coordinator will manage clinical research studies by coordinating and participating in a variety of complex activities involved in the collection, compilation ...
Kansas City, MO · On-site
$67K - $84K/yr
The Clinical Nurse Research Coordinator will manage clinical research studies by coordinating and participating in a variety of complex activities involved in the collection, compilation ...
The most popular types of Clinical Research Informatics jobs in Missouri are:
For Manager Clinical Research Informatics jobs in Missouri, the most frequently searched job titles are:
The top searched job categories for Manager Clinical Research Informatics jobs in Missouri are:
Cities in Missouri with the most Manager Clinical Research Informatics job openings:
$35 - $42/hr
Part-time
Medical, Life
Posted 18 days ago
8.1
Based on 53 frontline employees who took The Breakroom Quiz
63rd of 225 rated it services
Work Set-Up: On-site
Schedule Weekly Hours: 24 hours/week
About IQVIA
IQVIA is a global leader in advanced analytics, technology solutions, and clinical research services, dedicated to driving healthcare forward. We partner with the world's leading pharmaceutical, biotechnology, and medical device companies to improve patient outcomes and accelerate innovation. Our team combines deep scientific expertise with cutting-edge technology to deliver high-quality data and insights that shape the future of clinical trials.
About the Role
We are seeking a Clinical Research Coordinator (CRC) to join our team and support clinical research studies under the supervision of a principal investigator. This role involves hands-on clinical procedures, community outreach, and ensuring the highest standards of care and compliance.
Key Responsibilities
Perform a variety of clinical procedures, including ECG, sample collection, and vital signs.
Coordinate clinical research studies and maintain compliance with protocols and Good Clinical Practice (GCP) guidelines.
Support study conducts by preparing study materials, setting up equipment, and planning logistical activities.
Recruit, screen, and orient patients, ensuring their safety and well-being throughout the study.
Collect and accurately record clinical data in case report forms (CRFs).
Collaborate with investigators and monitors, addressing queries and ensuring data quality.
Act as a patient advocate and maintain a safe environment in accordance with Health and Safety policies.
Qualifications
Bachelor's degree preferred or equivalent combination of education and relevant experience.
Minimum 1+ years of relevant work experience in clinical research.
Working knowledge of clinical trials, GCP principles, and medical terminology.
Strong attention to detail and ability to establish effective working relationships.
Proficiency with EDC systems, data entry accuracy, and query management.
Please note: This position is not eligible for sponsorship.
IQVIA is a leading global provider of clinical research services, commercial insights and healthcare intelligence to the life sciences and healthcare industries. We create intelligent connections to accelerate the development and commercialization of innovative medical treatments to help improve patient outcomes and population health worldwide. Learn more athttps://jobs.iqvia.com
IQVIA is proud to be an equal opportunity employer. All qualified applicants will receive consideration for employment without regard to race, color, religion, sex, sexual orientation, gender identity, national origin, disability, status as a protected veteran, or any other status protected by applicable law. https://jobs.iqvia.com/eoe
IQVIA is committed to integrity in our hiring process and maintains a zero tolerance policy for candidate fraud. All information and credentials submitted in your application must be truthful and complete. Any false statements, misrepresentations, or material omissions during the recruitment process will result in immediate disqualification of your application, or termination of employment if discovered later, in accordance with applicable law. We appreciate your honesty and professionalism.
The potential base pay range for this role is $35.00-$42.00 per hour. The actual base pay offered may vary based on a number of factors including job-related qualifications such as knowledge, skills, education, and experience; location; and/or schedule (full or part-time). Dependent on the position offered, incentive plans, bonuses, and/or other forms of compensation may be offered, in addition to a range of health and welfare and/or other benefits.Sourced by ZipRecruiter
At IQVIA, we are passionate about helping customers and partners improve results and patient outcomes. Everything we do contributes to this vision for creating a healthier world. In today’s healthcare environment, it’s not only about how much data, information, and technology you have at your fingertips – it’s what you do with it. IQVIA is focused on making intelligent connections for customers across the entire healthcare ecosystem to help you drive healthcare forward. Whether that means partnering with novel technology companies to boost patient engagement, leveraging AI & machine learning to accelerate results, or using decentralized trials to reach the right patients wherever they are – we are always looking for smarter ways to move you forward.
Health care and social assistance
10,000+ Employees
Durham, NC, US