Top 1079 Clinical associate Jobs in St. Louis Mo

Clinical Research Coordinator
Eximia Clinical Research —St. Louis, MO
- Full-time
- English
- Microsoft Office
- Ability to sit for extended periods
- Health savings account
- Health insurance
Quick Apply
7d
Clinical Receptionist
The Retina Institute of St Louis, MO —St. Louis, MO
- $17 - $18 an hour
- Full-time
- Background check
- Private practice
- Microsoft Excel
- Free parking
- Paid training
Quick Apply
Clinical Office Coordinator
Shriners Hospitals for Children —St. Louis, MO
- $38.90 - $58.36 an hour
- Full-time
- 18 years or older
- BLS Certification
- Mid-level
Quick Apply
13d
Clinical Technician
Sam's Club —St. Louis, MO
- $23.50 - $31.50 an hour
- High school
- Merchandising
- Continuous improvement
- Paid jury duty
- Disability insurance
3d
Supply Chain Technician - Non-Clinical
SSM Health —St. Louis, MO
- Full-time
- Hospital
- Customer service
- No experience needed
- Paid parental leave
- Health insurance
2d
Patient Care Technician
DAVITA —St. Louis, MO
- Weekends as needed
- Outpatient experience
- High school diploma or GED
- Clinic
- Paid training
- Health insurance
7h
Patient Care Tech PRN
Orthopedic Surgery Center of Creve Coeur (13027) —Creve Coeur, MO
- Evenings as needed
- Surgery
- OSHA
- High school diploma or GED
Patient Dining Associate - Part Time (20 hours per week)
BJC HealthCare —St. Louis, MO
- $17.00 - $21.07 an hour
- Part-time
- Customer service
- No experience needed
- High school diploma or GED
- Disability insurance
- Health insurance
Clinical Research Coordinator I - Surgery
Washington University in St. Louis —St. Louis, MO
- $23.63 - $35.49 an hour
- Online Application
- Surgery
- Writing skills
- BLS Certification
- Commuter assistance
- Employee assistance program
Clinical Partner
SSM Health —St. Louis, MO
- 12 hour shift
- Nursing
- Vital signs
- Hospital
- Paid parental leave
- Health insurance
Clinical Research Study Assistant II (PRN) - Cardiology
Washington University in St. Louis —St. Louis, MO
- $19.93 - $29.93 an hour
- Part-time
- Writing skills
- Pass drug screening
- Laboratory experience
Medical Assistant
SSM Health —St. Louis, MO
- Full-time
- Vital signs
- BLS Certification
- No experience needed
- Paid parental leave
- Health insurance
Patient Dining Associate II - Part Time (20 hours per week)
BJC HealthCare —St. Louis, MO
- $17.25 - $22.33 an hour
- Part-time
- ServSafe
- Customer service
- No experience needed
- Disability insurance
- Health insurance
8d
Clinical Research Study Assistant II - Obstetrics and Gynecology
Washington University in St. Louis —St. Louis, MO
- $19.93 - $29.93 an hour
- Online Application
- Writing skills
- BLS Certification
- Pass drug screening
- Commuter assistance
- Employee assistance program
Clinical Research Coordinator I - Obstetrics and Gynecology
Washington University in St. Louis —St. Louis, MO
- $49,200 - $73,800 a year
- Online Application
- Clean driving record
- Writing skills
- BLS Certification
- Commuter assistance
- Employee assistance program
Clinical Research Coordinator I (Clinic) - Medical Oncology
Washington University in St. Louis —St. Louis, MO
- $49,200 - $73,800 a year
- Online Application
- Writing skills
- Medical office experience
- BLS Certification
- Commuter assistance
- Employee assistance program
Patient Care Technician - PCT
Fresenius Medical Care —Bridgeton, MO
- Full-time
- Inventory control
- Heavy lifting
- Laboratory experience
23h
Patient Care Technician - Patient Care Technician
Vibra Travels LLC —Chesterfield, MO
- $1,121 a week
- Online Application
- Computer literacy
- BLS Certification
- Mid-level
- Health insurance
- Referral program
Quick Apply
1d
Patient Care Associate II - Ob/Gyn
Washington University in St. Louis —St. Louis, MO
- $16.92 - $24.59 an hour
- Online Application
- Vital signs
- Writing skills
- BLS Certification
- Commuter assistance
- Employee assistance program
Clinical Research Coordinator I (Data) - Medical Oncology
Washington University in St. Louis —St. Louis, MO
- $49,200 - $73,800 a year
- Online Application
- BLS Certification
- Pass drug screening
- Office
- Commuter assistance
- Employee assistance program

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Clinical Research Coordinator

Eximia Clinical Research -
St. Louis, MO

Quick Apply

Job Details

Full-time
7 days ago

Benefits

Health savings account
Health insurance
Dental insurance
401(k)
Flexible spending account
Paid time off
Employee assistance program
Vision insurance
401(k) matching
Life insurance

Qualifications

Vascular access
Private practice experience
Clinical research
Injectable medication administration
Phlebotomy
Phone communication
Team leadership
Copy machines
English
Microsoft Office
Fax machines
Clinical trials
Multi-line phone systems
Productivity software
Faxing
Medical terminology
Technical Proficiency

Full Job Description

**PLEASE NOTE: Candidate must have direct CRC experience preferably at an embedded practice or a private research center**

The Clinical Research Coordinator II conducts and manages multiple clinical trials from start up through study close out in accordance with the study protocol, GCP, and Eximia Research Network’s SOPs.

Role & Responsibilities:

Conduct and manage clinical trials in accordance with the study protocol, GCP, ICH Guidelines and Eximia Clinical Network’s SOPs
Perform venipuncture, capillary puncture and/or other fluid collection within scope of the protocol and local law and regulations
Process, package and ship laboratory specimens as required per protocol and IATA regulations, if applicable
Implement and coordinate assigned clinical trials including start up, vendor management, subject recruitment, source development review, scheduling subjects, protocol training, collection of regulatory documents, conducting and participating in the ICF process(es), ensuring data is entered in a timely manner and all queries are resolved, managing and reporting adverse events, serious adverse events, and deviations, implementing new protocol amendments, providing all close outreports.
Apply project management concepts to manage risk and improve quality in the conduct of a clinical research study
Develop, coordinate, and implement research and administrative strategies to successfully manage assigned protocols.
Communicate effectively and professionally with coworkers, leadership, study subjects, sponsors, CROs, and vendors.
Apply good documentation in accordance with ALCOA-C principles when collecting and correcting data, transferring data to sponsor/CRO data capture systems and resolving queries
Maintain confidentiality of patient protected health information, sponsor confidential information and Eximia Clinical Network confidential information
Verify and escalate patient safety concerns by ensuring all adverse events, serious adverse events, and adverse events of special interest are followed and reported in accordance with the protocol and Eximia Clinical Network SOPs.
Ensure all data is entered into the sponsor's data portal and all queries are resolved in a timely manner as set forth in Clinical Trial Agreement
Ensure staff are delegated and trained appropriately and documented
Create, collect and submit regulatory documents to Sponsors and IRBs as required per protocol, GCP/ICH regulations and IRB requirements.
Evaluate potential subjects for participation in clinical trials including phone and in person prescreens.
Create and execute recruitment strategies defined by Clinical Research Team
Understand key timelines, endpoints, required vendors, and patient population for each assigned protocol.
Understand product development lifecycle and significance of protocol design including critical data points
Understand the disease process or condition under study
Collaborate with Clinical Research Team to develop Quality Control strategy for reviewing one’s work on an ongoing basis and in preparation for monitor visits.
Perform clinical duties (e.g., drug preparation and administration, fibroscan, phlebotomy, ECG, lab processing) within scope
Other duties as assigned

Qualifications

Education/Experience:

Bachelor’s degree and 2 years relevant experience in the life science industry OR
Associate’s degree with 4 years relevant experience in the life science industry OR
High School Graduate and/or technical degree with minimum of 6 years relevant experience in the life science industry AND1 year Clinical Research Coordinator experience

Required Licenses/Certifications:

Phlebotomy if applicable and required by state law
Intramuscular dose administration and preparation if applicable and required by state law
Certified Clinical Research Coordinator through ACRP or SOCRA within six months of being in the role

Required Skills:

Demonstrated knowledge of medical terminology
Proficient in the use of the following technology: Computers, Microsoft Office software, fax, copier, and multi-line telephone.
Proficient ability to work in a fast-paced environment
Proficient verbal, written, and organizational skills
Proficient interpersonal and communication skills
Proficient ability to work as a team player
Proficient ability to read, write, and speak English
Proficient ability to multi-task
Proficient ability to follow written guidelines
Proficient ability to work independently, plan and prioritize with minimal guidance
Proficient ability to be flexible/adapt as daily schedule may change rapidly
Must be detail oriented
Demonstrated problem solving and strategic decision making ability.
Proficient in accepting individual responsibility for actions taken and demonstrating professionalism when judged, critiqued and/or praised.
Demonstrated leadership ability

Required Physical Abilities:

Sit or stand for long periods of time
Travel locally and nationally
Communicate in person and by a telephone
Limited to moderate walking required
Limited to lifting up to 30 pounds

Job Type: Full-time

Benefits:

401(k)
401(k) matching
Dental insurance
Employee assistance program
Flexible spending account
Health insurance
Health savings account
Life insurance
Paid time off
Vision insurance

Experience:

CRC work at embedded practice or private research center: 2 years (Required)

Ability to Commute:

St. Louis, MO 63141 (Required)

Work Location: In person

Quick Apply

Refine Your Search

clinical associate jobs in st. louis mo

Clinical Research Coordinator

Clinical Receptionist

Clinical Office Coordinator

Clinical Technician

Supply Chain Technician - Non-Clinical

Patient Care Technician

Patient Care Tech PRN

Patient Dining Associate - Part Time (20 hours per week)

Clinical Research Coordinator I - Surgery

Clinical Partner

Clinical Research Study Assistant II (PRN) - Cardiology

Medical Assistant

Patient Dining Associate II - Part Time (20 hours per week)

Clinical Research Study Assistant II - Obstetrics and Gynecology

Clinical Research Coordinator I - Obstetrics and Gynecology

Clinical Research Coordinator I (Clinic) - Medical Oncology

Patient Care Technician - PCT

Patient Care Technician - Patient Care Technician

Patient Care Associate II - Ob/Gyn

Clinical Research Coordinator I (Data) - Medical Oncology

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