Top 228 Clinical trial Jobs in Missouri

Clinical Trial Assistant
Geneoscopy LLC —St. Louis, MO
- Full-time
- Google Workspace
- Nursing
- Writing skills
- Health insurance
- Dental insurance
Quick Apply
Clinical Research Coordinator – Wan Lab
University of Missouri —Columbia, MO
- $59,322 - $96,762 a year
- Full-time
- Nursing
- Inventory management
- HIPAA
- Paid parental leave
- Disability insurance
Licensed Clinical Social Worker
Hermann Area District Hospital —Hermann, MO
- $30 - $40 an hour
- Part-time
- Master of Social Work
- BLS Certification
- Licensed Clinical Social Worker
- Flexible schedule
Quick Apply
MedTech Part Time Clinical Consultant – St. Louis, MO West
IQVIA —St. Louis, MO
- $60 an hour
- Part-time
- RN License
- Mid-level
- 3 years
Special Agent: Healthcare Services/Medical Background
Federal Bureau of Investigation —St. Louis, MO
- $103,326 - $133,200 a year
- Full-time
- Mid-level
- Bachelor's degree
- Travel
13d
Special Agent: Healthcare Services/Medical Background
Federal Bureau of Investigation —Jackson, MO
- $103,326 - $133,200 a year
- Full-time
- Mid-level
- Bachelor's degree
- Travel
13d
Special Agent: Healthcare Services/Medical Background
Federal Bureau of Investigation —Kansas City, MO
- $103,326 - $133,200 a year
- Full-time
- Mid-level
- Bachelor's degree
- Travel
13d
Clinical Trial Assistant
EVERSANA —Chesterfield, MO
- Full-time
- Office
- High school diploma or GED
- Travel
Quick Apply
Clinical Trial Recruiter
QPS, LLC —Springfield, MO
- Full-time
- Office
- High school diploma or GED
- Recruiting
- Paid holidays
- Disability insurance
Quick Apply
Clinical Research Assistant - Cancer Center
The University of Kansas Medical Center —Kansas City, MO
- $22.88 - $33.17 an hour
- Full-time
- Nursing
- Computer literacy
- Bachelor's degree
- Paid jury duty
- Paid holidays
Clinical Research Nurse
University of Missouri —Columbia, MO
- $75,300 - $85,000 a year
- Online Application
- Nursing
- Blood sampling
- Surgery
- Paid parental leave
- Disability insurance
Clinical Research Coordinator - Women's Health Department
University Health KC —Kansas City, MO
- Full-time
- Hospital
- Computer literacy
- HIPAA
Clinical Data Abstractor Specialist
SSM Health —St. Louis, MO
- Full-time
- Anatomy knowledge
- Mid-level
- Bachelor's degree
- Paid parental leave
- Health insurance
Clinical Research Coordinator
BJC HealthCare —St. Louis, MO
- $21.58 - $35.84 an hour
- Full-time
- Acute care
- Mid-level
- Bachelor's degree
- Disability insurance
- Health insurance
Clinical Research Coordinator I/II/III Opportunities – Multiple Locations Nationwide
Headlands Research —St. Louis, MO
- $45,000 - $100,000 a year
- Bachelor's degree
- Psychology
- Communication skills
Quick Apply
Medical Scientific Liaison
Thermo Fisher Scientific —Missouri
- Full-time
- English
- Mid-level
- Office
5d
Clinical Research Coordinator - Jefferson City, MO
IQVIA —Jefferson City, MO
- $35 - $42 an hour
- Part-time
- Vital signs
- Office
- Bachelor's degree
11d
Clinical Research Coverage Analyst
Saint Louis University —St. Louis, MO
- Full-time
- Nursing
- 5 years
- Mid-level
Quality Manager
Headlands Research —Chesterfield, MO
- $110,000 - $140,000 a year
- Remote
- 5 years
- Mid-level
- Travel
Quick Apply
2d
Clinical Education Specialist- Ultrasound (St. Louis, MO)
GE HEALTHCARE —Missouri
- Anatomy knowledge
- Hospital
- Computer literacy
- Relocation assistance
- Health insurance

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Clinical Trial Assistant

Geneoscopy LLC -
St. Louis, MO

Quick Apply

Job Details

Full-time

Benefits

Stock options
Health insurance
Dental insurance
Paid time off
Vision insurance
401(k) matching
Life insurance

Qualifications

Electronic health records (EHR) management
Professional ethics
Writing skills
HIPAA
Laboratory experience
Health information regulatory compliance
Adobe Acrobat
File organization

Full Job Description

Clinical Trial Assistant

This is an on-site, in-office position at Geneoscopy HQ in St. Louis, Missouri.

The Clinical Trial Assistant (CTA) provides administrative and operational support for clinical research studies conducted in accordance with federal regulations, Good Clinical Practice (GCP), institutional policies, and study protocols. The CTA assists research coordinators, project managers, investigators, sponsors, and study participants by maintaining regulatory documentation, coordinating study activities, tracking study milestones, and ensuring accurate data and records management.

This position serves as an integral member of the clinical research team and contributes to the successful execution of clinical trials while maintaining participant confidentiality and regulatory compliance.

RESPONSIBILITIES

Study Administration:
- Assist with day-to-day coordination of clinical research studies
- Schedule study visits, calls, and participant follow-up activities
- Prepare study materials and participant packets (informed consents)
- Coordinate shipment and receipt of study supplies
- Track study enrollment and participant status
- Maintain study calendars and visit schedules
Regulatory Support:
- May assist with maintaining Investigator Site Files (ISF) and regulatory binders.
- May assist with IRB submissions, amendments, continuing reviews, and reportable events
- Organize essential documents according to GCP guidelines
- Track regulatory approvals and expiration dates
- Ensure study documentation is complete and audit-ready
Data Management:
- Assist with entry of study data into electronic data capture (EDC) systems
- Review source documentation for completeness
- Assist with query resolution
- Maintain study tracking logs and screening logs
- Ensure timely and accurate documentation
Participant Support:
- Assist with participant recruitment activities
- Conduct reminder phone calls, emails, and appointment confirmations
- Prepare informed consent documents for coordinator review
- Collect questionnaires and study forms
- Maintain participant confidentiality in accordance with HIPAA regulations
Laboratory and Specimen Support:
- Prepare specimen collection kits
- Coordinate specimen shipping
- Maintain specimen inventory logs
- Track laboratory supplies
Administrative:
- Maintain study correspondence
- Assist with sponsor monitoring visits and audits
- Coordinate document requests
Compliance:
- Follow Good Clinical Practice (ICH-GCP) guidelines.
- Maintain HIPAA compliance.
- Adhere to institutional SOPs.
- Protect participant confidentiality.
- Complete required research training.
- Support quality assurance initiatives.
- Assist during internal and external audits.
Other duties as assigned.

EDUCATION REQUIREMENTS

Bachelor's degree in Biology, Health Sciences, Public Health, Nursing, Psychology, or a related field is preferred.
- Associate's degree with relevant work experience may be considered.

QUALIFICATIONS

Possess 0-2 years of clinical research experience in a healthcare, laboratory, or administrative setting.
Demonstrate a basic understanding of clinical research processes, Good Clinical Practices (GCPs), HIPAA regulations, IRB requirements, and the informed consent process.
Exemplify hands-on experience with Google Workspace, Adobe Acrobat, Database management, and file organization.
- Knowledge of Electronic Medical Records (EMR) and Electronic Data Capture (EDC) systems.
Exemplify the ability to multitask and thrive in an agile, fast-paced, deadline-driven environment while remaining flexible, proactive, resourceful, and efficient.
Possess proficient verbal and written communication skills, while willing to share and receive information and ideas from all levels of the organization to achieve the desired results.
Possess high ethics and conduct business in the most professional manner.
Seek inclusiveness and collaboration but step up to responsibility, make tough decisions, and be accountable for those decisions.
Act as a results-oriented team player with strong interpersonal and communication skills, capable of working collaboratively with colleagues.
Preferred Additional Experience:
- CITI Human Subjects Protection training
- GCP certification
- Supporting FDA-regulated clinical trials
- Reading medical records/pathology reports
- Clinical trial documentation
- Collaborating with sponsors or Vendors

SCHEDULE
This is a salaried position, requiring at least 40 hours per week. There may be projects that require activities beyond the standard hours.

COMPENSATIONBENEFITS

Base salary range: annually determined based on the candidate's experience, knowledge, and abilities.
Bonus: discretionary annual bonus based on a percentage of the employee's base salary
Benefits: health, vision, dental, life insurance, 401k (with employer match), and paid time off.
Company stock options

ADDITIONAL INFORMATION

Geneoscopy's Core Values
Ability to embody Geneoscopy's beliefs, philosophies, and principles:

Integrity - we do the right thing through our words, actions, and behaviors
Courage - step up, speak up, stand out
Agility - think and act fast, embracing change
Passion - for our customers, our people, our work, and for excellence
Collaboration - our differences are assets

Physical Demands

Employees may be required to lift routine office supplies and use standard office equipment.
Must possess the ability to sit and/or stand for long periods.
Must possess the ability to perform repetitive motion.

Work Environment

May have exposure to fumes anbiohazardousus material in the laboratory environment.
May be required to handle blood-borne pathogens and general laboratory reagents.

By completing this online employment application, you certify that the information on this application is true and complete to the best of your knowledge. You understand that any misrepresentation or omission of fact in response to any inquiry made in this application may result in the rejection of the application or if hired, dismissal whenever it is discovered. You authorize and release all parties from any liability or damage that may result from seeking, furnishing, or using such information. You understand and agree that, if hired, your employment is for no definite period and may, regardless of the date of payment of compensation, be terminated by Geneoscopy at any time, for any or no reason, with or without notice. You understand that no representation to the contrary is valid unless in writing, setting a definite term of employment, and signed by the company's CEO. You further understand and agree that any job offer is contingent upon your passing, to the company's satisfaction, a criminal background check, reference checks, and other possible screenings. You understand that this application is active for 90 days only, and if you do not hear from the company but still wish to be considered for employment after 90 days, you will need to fill out a new application.

Quick Apply

Refine Your Search

clinical trial jobs in missouri

Clinical Trial Assistant

Clinical Research Coordinator – Wan Lab

Licensed Clinical Social Worker

MedTech Part Time Clinical Consultant – St. Louis, MO West

Special Agent: Healthcare Services/Medical Background

Special Agent: Healthcare Services/Medical Background

Special Agent: Healthcare Services/Medical Background

Clinical Trial Assistant

Clinical Trial Recruiter

Clinical Research Assistant - Cancer Center

Clinical Research Nurse

Clinical Research Coordinator - Women's Health Department

Clinical Data Abstractor Specialist

Clinical Research Coordinator

Clinical Research Coordinator I/II/III Opportunities – Multiple Locations Nationwide

Medical Scientific Liaison

Clinical Research Coordinator - Jefferson City, MO

Clinical Research Coverage Analyst

Quality Manager

Clinical Education Specialist- Ultrasound (St. Louis, MO)

I want to receive the latest job alert for clinical trial in missouri

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