Top 13 Trial administrator Jobs in St. Louis, Mo

Clinical Research Coordinator
Ophthalmology Associates —Des Peres, MO
- Part-time
- Background check
- Anatomy knowledge
- Microsoft Outlook
- Mileage reimbursement
- Paid parental leave
Quick Apply
Clinical Research Coordinator IV (Hybrid) - Ophthalmology
Washington University in St. Louis —St. Louis, MO
- $64,300 - $99,700 a year
- Online Application
- Hybrid work
- BLS Certification
- Pass drug screening
- Office
- Commuter assistance
- Employee assistance program
4d
Senior Research Program Manager (Hybrid) - Emergency Medicine
Washington University in St. Louis —St. Louis, MO
- $77,700 - $120,400 a year
- Weekends as needed
- Hybrid work
- Pass drug screening
- English
- Office
- Commuter assistance
- Employee assistance program
Clinical Research Coordinator
Eye Care Partners Career Opportunities —Des Peres, MO
- Part-time
- Background check
- Anatomy knowledge
- Microsoft Outlook
- Mileage reimbursement
- Paid parental leave
Quick Apply
Clinical Research Coverage Analyst
Saint Louis University —St. Louis, MO
- Full-time
- Nursing
- 5 years
- Mid-level
Grant Specialist II - Pediatrics Central Administration
Washington University in St. Louis —St. Louis, MO
- $53,100 - $90,600 a year
- Online Application
- Hybrid work
- Computer literacy
- Pass drug screening
- Mid-level
- Commuter assistance
- Employee assistance program
4d
Senior Director, Market Development and Intelligence – Heartland
Spectrum —St. Louis, MO
- Full-time
- Marketing
- English
- Residential
- Opportunities for advancement
Practice Administrator - Hospital Medicine - SSM St. Clare
Vituity —Fenton, MO
- Per diem
- Microsoft Outlook
- Hospital
- Customer service
- Profit sharing
- Wellness program
1d
Practice Administrator - Hospital Medicine - HSHS St. Elizabeth's Hospital
Vituity —O'Fallon, IL
- $23.40 - $29.25 an hour
- Full-time
- Microsoft Outlook
- Customer service
- English
- Profit sharing
- Wellness program
10d
Senior Associate Attorney
Stanton | Barton —St. Louis, MO
- Full-time
- Writing skills
- English
- Mid-level
- Health insurance
- Dental insurance
Research Nurse Coordinator Specialist - Obstetrics and Gynecology
Washington University in St. Louis —St. Louis, MO
- $68,700 - $123,600 a year
- Online Application
- Nursing
- RN License
- Computer literacy
- Commuter assistance
- Employee assistance program
Partner - First-Party Commercial Property Insurance Coverage
Lewis Brisbois —St. Louis, MO
- Full-time
- Hybrid work
- 8 years
- Contracts
- Senior level
- Health insurance
- Dental insurance
2d
Senior AI Engineer - SFL Scientific
Deloitte —St. Louis, MO
- $128,000 - $252,500 a year
- Full-time
- Computer science
- Azure
- Computer Science

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Clinical Research Coordinator IV (Hybrid) - Ophthalmology
Washington University in St. Louis —St. Louis, MO
More than one credential, certification or professional license may be required depending on the role. A driver's license is not required for this position.
$64,300 - $99,700 a year
4d

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Clinical Research Coordinator

Ophthalmology Associates -
Des Peres, MO

Quick Apply

Job Details

Part-time | Seasonal | Full-time

Benefits

Mileage reimbursement
Paid parental leave
Paid holidays
Health insurance
Dental insurance
Paid time off
Parental leave
Vision insurance
401(k) matching
Employee discount
Life insurance

Qualifications

Computer literacy
High school diploma or GED

Full Job Description

**This is a full-time, long-term position. Unfortunately, we CANNOT accommodate students looking for only a summer job or that would need to work part-time during the school year.**

Job Title: Clinical Research Coordinator
Company: Ophthalmology Associates
Location: Des Peres, MO
Travel: Travel to our other clinics in the St Louis metro area and Sullivan, MO will be required as needed. We do pay mileage reimbursement!

Perks

Full Benefits Package - Medical, Vision, Dental and Life Insurance
401k + Employer Matching
Paid Time Off (PTO) and Paid Holidays
Competitive Base Pay
Paid Maternity Leave
Employee Discounts

Hours:

Full Time
Our offices are open Monday-Friday 8am-5pm
- 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 operations of clinical trials.

Duties include administration; project implementation, meeting support, quality assurance, and dissemination of results, recruitment; collection, recording, and editing of interview, questionnaire, and clinical data; performing quality assurance monitoring of study data; randomization of study participants; conducting case management tasks; scheduling participant appointments; supporting clinical and group intervention; review medical records following study protocols; and performing other duties in support of clinical trials services as assigned.

ESSENTIAL DUTIES AND RESPONSIBILITIES

Provide assistance in the administrative, technical and scientific day-to-day operation of the study to assure project goals and timelines are met, quality data is collected and managed, and to assure participant and/or data confidentiality.
Conduct clinical research as outlined in the study protocol. Maintain knowledge of clinical research issues. Follow GCP guidelines. Implement confidentiality and privacy regulations.
Evaluate protocols, assist in study selection, correspond/coordinate with the sponsor/CRO and prepare study budgets.
Support and assist Research personnel in the operation of equipment used in clinical trials.
Support the development of Quality Assurance procedures, and assist with the monitoring of data collection and data transfers. Assist with the preparation of annual IRB reviews.
Support the Project Director, Clinic Coordinator, or PI in the administration of the grant/contract per federal rules and regulations and/or specific grant/contract language. Understand the operational budget and sub-contracts; track documentation and authorization of payment of study related bills. Provide assistance in the preparation of project reports for PI review and approval.
Recruit study participants to a broad range of studies using specific study protocols to contact, screen, and determine eligibility and schedule appointments with study participants.
Collect, edit and record/enter study data via interview, structured interview, questionnaire, medical record review, and basic clinical measurements for complex study protocols, and perform technical duties as assigned.
Support orientation and structured intervention sessions in accordance with technical training and certification(s).
Assist with case management activities to support the work of the project(s).
Support the process of summarizing and sharing project information with other sites. Support the Project Director, Clinic Coordinator, and/or PI in the maintaining regular contact with other Project Administrators in order to share information and ideas. Assist with the tracking of papers in process for projects, with planning for project papers and posters to be presented at national and international conferences.
Adheres to all safety policies and procedures in performing job duties and responsibilities while supporting a culture of high quality and great customer service.
Perform other duties in support of clinical trials services as assigned.

QUALIFICATIONS

Demonstrated interpersonal, communication and interviewing skills with people of all ages.
Organized, detail oriented, self-directed and dependable.
Able to prioritize work, solve problems and work independently.
Able to function in a team environment and use negotiation skills.
Favorable result on background check required.
Must be able to provide proof of identity and right to work in the United States.

EDUCATION AND/OR EXPERIENCE

High school diploma or general education degree (GED) required
Undergraduate degree in a related field preferred
At least one (1) year of experience collecting information using one of the following methods:
- Telephone/face-to-face interviews
- Working with patients and study participants in a clinical situation (proficiency in refracting patients needed)
One year of experience collecting or processing data for research or Quality Assurance purposes
Working knowledge of medical terminology, anatomy, and disease processes; medical record organization and interpretation
Experience in health research or research data collection is preferred
Familiarity with classification of disease processes is preferred
Knowledge of basic research ethics and principles is preferred

LICENSES AND CREDENTIALS

Minimum Required: None

SYSTEMS AND TECHNOLOGY

Proficient in Microsoft Excel, Word, PowerPoint, Outlook
Basic knowledge of computer functions
Able to use computers and software programs for complex tracking of participant tasks

PHYSICAL REQUIREMENTS

This role requires a variety of physical activities to effectively perform essential job functions. The position involves frequent walking (75%), sitting (50%), and standing (50%), with regular bending, stooping, and reaching (25–50%). Employees must be able to lift, carry, push, and pull items up to 25 lbs. Strong fine motor skills and full use of hands are essential, as the role demands constant grasping, writing/typing, and use of technology. Visual and auditory acuity—including color, depth, peripheral vision, and the ability to adjust focus—is required 100% of the time. Occasional driving or climbing may also be necessary.

If you need assistance with this application, please contact (636) 227-2600. Please do not contact the office directly – only resumes submitted through this website will be considered.

EyeCare Partners is an equal opportunity/affirmative action employer. All applicants will be considered for employment without attention to race, color, religion, sex, sexual orientation, gender identity, national origin, veteran or disability status.

Quick Apply

Refine Your Search

trial administrator jobs in st. louis, mo

Clinical Research Coordinator

Clinical Research Coordinator IV (Hybrid) - Ophthalmology

Senior Research Program Manager (Hybrid) - Emergency Medicine

Clinical Research Coordinator

Clinical Research Coverage Analyst

Grant Specialist II - Pediatrics Central Administration

Senior Director, Market Development and Intelligence – Heartland

Practice Administrator - Hospital Medicine - SSM St. Clare

Practice Administrator - Hospital Medicine - HSHS St. Elizabeth's Hospital

Senior Associate Attorney

Research Nurse Coordinator Specialist - Obstetrics and Gynecology

Partner - First-Party Commercial Property Insurance Coverage

Senior AI Engineer - SFL Scientific

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