Top 16 AMR Jobs | SimplyHired

Research Assistant
AMR Clinical —Lexington, KY
- Overtime
- English
- Mid-level
- Clinic
Quick Apply
Sub-Investigator - Nurse Practitioner/Physician Assistant
AMR Clinical —Knoxville, TN
- Full-time
- English
- Mid-level
- 3 years
Quick Apply
Senior CRC
AMR Clinical —Myrtle Beach, SC
- Overtime
- Vital signs
- English
- 3 years
- Flexible schedule
Quick Apply
Research Assistant - Medical Assistant
Alliance For MultiSpecialty Research LLC —Knoxville, TN
- Overtime
- English
- Mid-level
- Clinic
Quick Apply
Clinical Research Coordinator 1
Alliance For MultiSpecialty Research LLC —Doral, FL
- Overtime
- Vital signs
- English
- Mid-level
Quick Apply
Data Management Specialist
AMR Clinical —Mobile, AL
- Full-time
- Computer literacy
- Mid-level
- Organizational skills
Quick Apply
1d
Research Assistant - Medical Lab Technician (Night Shift)
Alliance For MultiSpecialty Research LLC —Knoxville, TN
- Overtime
- Mid-level
- Clinic
- Organizational skills
Quick Apply
Chief Operating Officer
Alliance For MultiSpecialty Research LLC —Raleigh, NC
- Full-time
- Medicine
- 11+ years
- English
Quick Apply
Regulatory Manager
AMR Clinical —United States
- Full-time
- Remote
- 5 years
- Word processing
- English
Quick Apply
HR Manager
Alliance For MultiSpecialty Research LLC —United States
- Full-time
- Remote
- Word processing
- English
- Master's degree
Quick Apply
12d
Senior Project Management
Alliance For MultiSpecialty Research LLC —United States
- Full-time
- Remote
- 5 years
- Master's degree
- Presentation skills
Quick Apply
Budget Specialist
AMR Clinical —United States
- Full-time
- Remote
- Word processing
- English
- Mid-level
Quick Apply
1d

Discover related jobs

Based on your search for AMR jobs.

EMT
SeniorCare —Monticello, NY
Must possess a valid driver’s license. Responsible for maintaining NYS DOH certification. Administers basic pre-hospital care within the limits of certification…
$20 - $25 an hour
Quick Apply
(Part Time) Emergency Medical Technician (EMT-B / EMT-A)
Join Parachute —Pine Bluff, AR
Certified/licensed EMT (Advanced or Basic) in the state of employment. Current BLS or CPR certification. Manage health logs and test results with clinical…
Quick Apply

I want to receive the latest job alert for AMR

By signing in to your account, you agree to SimplyHired's Terms of Service and consent to our Cookie and Privacy Policy.

Explore jobs in more locations

AMR jobs near

Chief Operating Officer jobs in Raleigh, NC

Clinical Research Coordinator jobs in Doral, FL

Research Assistant jobs in Lexington, KY

Data Specialist jobs in Mobile, AL

Research Assistant jobs in Knoxville, TN

Laboratory Technician jobs in Knoxville, TN

Nurse Practitioner jobs in Knoxville, TN

Chief Operating Officer jobs in Nashville, TN

Foia Officer jobs in Chicago, IL

Chief Operating Officer jobs in Huntington Beach, CA

Chief Operating Officer jobs in Trenton, NJ

Chief Operating Officer jobs in Colorado Springs, CO

Security Officer jobs in Savannah, GA

Regulatory Project Manager jobs in San Jose, CA

Household Manager jobs in Denver, CO

Regulatory Project Manager jobs in Houston, TX

Restaurant General Manager jobs in Austin, TX

Regulatory Project Manager jobs in Research Triangle Park, NC

Regulatory Project Manager jobs in Columbus, OH

Clinical Research Coordinator jobs in Charlotte, NC

Research Assistant

AMR Clinical -
Lexington, KY

Quick Apply

Job Details

Full-time

Qualifications

Laboratory sample storage
Report preparation
Incident reporting compliance
Healthcare incident report preparation
Medical chart preparation
Laboratory procedures
Regulatory documents
Informed consent
Pre-examination patient preparation
Medical equipment operation
EKG
Adverse event reporting
Patient transfer methods
Labeling
Safety regulations
Maintaining patient confidentiality
Filing
Client file management
English
Phlebotomy specimen handling
Mid-level
Healthcare practice inventory management
Patient safety
Medication supplies
Task prioritization
Adverse drug reaction monitoring
Laboratory compliance
Informed consent procedures implementation
Medical record retrieval
Document review

Full Job Description

The role of the Research Assistant is responsible for performing a wide variety of administrative and clinical tasks to support the study site. The Research Assistant supports all study related activities to ensure that the study is completed accurately per study protocol. The Research Assistant is an integral role to assist with the flow of the clinic.

To consistently embody AMR Clinical’s Core Values:

United We Achieve
Celebrate Diverse Perspectives
Do the Right Thing
Adapt and Persevere

The Research Assistant reports to the Site Manager/Team Lead.

Classification: Non-Exempt

Primary Responsibilities:

Effectively prioritize tasks and meet deadlines in a fast-paced environment.
Maintain a strong emphasis on compliance responsibilities, including timely identification and reporting of protocol deviations, serious adverse events (SAEs), and adherence to regulatory and site-specific requirements.
Monitor & Report Adverse Events – Recognize and promptly report AEs, protocol deviations, and safety concerns to the clinical team. Document AEs and Serious Adverse Event reporting in compliance with FDA, IRB, and sponsor requirements, ensuring timely follow-up and resolution.
Ensure Compliance with Study Protocols & Regulatory Guidelines – Adhere to Good Clinical Practice (GCP), FDA regulations, and site SOPs when conducting study-related activities.
Assist in Subject Retention Efforts – Support ongoing engagement, communication, and compliance to enhance subject retention throughout the study.
Perform Inventory Management – Track and manage study supplies, lab kits, and investigational products (if applicable) to ensure readiness for study visits.
Assist in maintaining accurate, timely, and audit-ready documentation of all study-related activities.
Perform Laboratory Responsibilities with Accuracy – Ensure proper labeling, handling, storage and shipment of specimens per protocol and regulatory requirements.
Strong problem-solving skills and ability to adapt to evolving study requirements.
Ability to handle confidential and sensitive information with discretion.
Ability to follow detailed instructions and maintain high levels of accuracy.
Establish and maintain patient rapport during clinical drug trials to include management of subjects
- Clinical data collection such as vital signs, EKG recording, subject weights, etc.
- Medical record retrieval and review when required
- Subject interviews
- Phlebotomy
- Filing and pulling study records
- Answering and triage of research office calls
- Subject check in and out process
Study preparation, such as screening packets, preparing informed consents, pulling charts for the next business day, etc.
Filing study documents in the subject’s chart.
Develop rapport with study sponsors, monitors, study participants, etc.
Assist monitors during onsite visits
Maintain accurate enrollment/ICF logs
Assist the clinical team to complete study activities. The clinical team includes but is not limited to CRCs, Laboratory, Data management, etc
Educate subjects on diaries as studies require.
Accurate and timely documentation
Unblinded duties as assigned.
Position may require occasional weekend and/or overtime hours.
Other duties as assigned

Desired Skills and Qualifications:

Medical office experience, medical certificate, or equivalent work experience preferred.
Phlebotomy skills are preferred
Excellent attention to detail
Strong listening, verbal and written communication skills
Excellent task management and organizational skills
Ability to multi-task in an always evolving fast paced environment.
Demonstrate proficient knowledge of operating office equipment and software.
Ability to be ambulatory most of the workday.
Ability to lift/transfer/push/manipulate equipment and patients, which requires strength, gross motor and fine motor coordination.
Fluent in English.

AMR Clinical does not discriminate in employment on the basis of race, color, religion, sex (including pregnancy and gender identity), national origin, political affiliation, sexual orientation, marital status, disability, genetic information, age, retaliation, parental status, military service, or other non-merit factor.

** This job description is intended to be a representative summary of the major responsibilities and accountabilities of the staff holding this position. The staff may be requested to perform job-related tasks other than those stated in this description.

Quick Apply

Refine Your Search

AMR jobs

Research Assistant

Sub-Investigator - Nurse Practitioner/Physician Assistant

Senior CRC

Research Assistant - Medical Assistant

Clinical Research Coordinator 1

Data Management Specialist

Research Assistant - Medical Lab Technician (Night Shift)

Chief Operating Officer

Regulatory Manager

HR Manager

Senior Project Management

Budget Specialist

Discover related jobs

I want to receive the latest job alert for AMR

Explore jobs in more locations

Job Seeker Tools

Employer Tools

Browse

Stay Connected