Top 18 AMR Jobs | SimplyHired

Sub-Investigator - Nurse Practitioner/Physician Assistant
AMR Clinical —Knoxville, TN
- Full-time
- English
- Mid-level
- 3 years
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Senior CRC
AMR Clinical —Myrtle Beach, SC
- Overtime
- Vital signs
- English
- 3 years
- Flexible schedule
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Research Assistant - Medical Assistant
Alliance For MultiSpecialty Research LLC —Knoxville, TN
- Overtime
- English
- Mid-level
- Clinic
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Research Assistant
AMR Clinical —Lexington, KY
- Overtime
- English
- Mid-level
- Clinic
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Data Management Specialist
AMR Clinical —Mobile, AL
- Full-time
- Computer literacy
- Mid-level
- Organizational skills
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6d
Clinical Research Coordinator 1
Alliance For MultiSpecialty Research LLC —Doral, FL
- Overtime
- Vital signs
- English
- Mid-level
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Chief Operating Officer
Alliance For MultiSpecialty Research LLC —Raleigh, NC
- Full-time
- Medicine
- 11+ years
- English
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Research Assistant - Medical Lab Technician (Night Shift)
Alliance For MultiSpecialty Research LLC —Knoxville, TN
- Overtime
- Mid-level
- Clinic
- Organizational skills
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HR Manager
Alliance For MultiSpecialty Research LLC —United States
- Full-time
- Remote
- Word processing
- English
- Master's degree
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Budget Specialist
AMR Clinical —United States
- Full-time
- Remote
- Word processing
- English
- Mid-level
Quick Apply
6d
Regulatory Manager
AMR Clinical —United States
- Full-time
- Remote
- 5 years
- Word processing
- English
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Senior Project Management
Alliance For MultiSpecialty Research LLC —United States
- Full-time
- Remote
- 5 years
- Master's degree
- Presentation skills
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Coder Auditor/Senior CDI Specialist
HAMASPIK CHOICE INC —Brooklyn, NY
Ability to identify areas of over or under utilization and work with team and physician groups to develop processes to avoid.
$83,000 - $90,000 a year
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Senior CRC
AMR Clinical —Myrtle Beach, SC
Proactively collaborates with QA and Site Manager to develop and implement corrective and preventive action plans to mitigate risks and improve study outcomes.
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Sub-Investigator - Nurse Practitioner/Physician Assistant

AMR Clinical -
Knoxville, TN

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Job Details

Full-time

Qualifications

Data integrity assurance
Adverse event reporting
Clinical incident reports
Team leadership
Pharmaceutical regulatory compliance
English
Mid-level
3 years
Patient safety
Research project team management
Data integrity and documentation
ICH guidelines
Professional clinical test scoring
Research safety & compliance
Nurse Practitioner (NP)
Task prioritization
Clinical training
Team training
Adverse drug reaction monitoring
Compliance documentation
Medical License
Clinical team leadership
Clinical quality assurance standards
Research participation
Clinical trial support in drug product development
Task assignment
Pharmaceutical research experience
Leadership
Delegation
Mechanism of action

Full Job Description

Sub- Investigator Position Description

Position Overview

The Sub Investigator is responsible for conducting clinical trials in accordance with the research protocol, Good Clinical Practices (GCP), and federal/state regulations. The Sub Investigator will collaborate with the study team, as well as various medical pharmaceutical companies, and regulatory personnel to ensure the health and welfare of study subjects under the direction of the Principal Investigator.

To consistently embody AMR Clinical’s Core Values:

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

Shift Details: Monday-Friday 7:00-3:30pm with occasional on call appointments.

The Sub Investigator reports to the Principal Investigator.

Classification: Exempt

Primary Responsibilities:

Maintain a current license to practice medicine.
Assume responsibility as the Sub Investigator for the duration of the clinical trials.
Conduct testing and rating scales per sponsors instructions and protocols.
Completion of documentation, paper and electronic as required per protocol.
Provide detailed study related documentation as required and ensure data integrity.
Perform evaluations on subjects as needed per the protocol.
Perform physicals per study protocol, as needed.
Perform and review ratings performed by outside physicians, as needed in accordance with the study protocol.
Evaluate subjects for clinical research trials based on their past medical and psychiatric history compared to inclusion and exclusions per study protocol.
Evaluate subject safety and compliance with investigational product as specified by protocol.
Evaluate and report all serious adverse events (SAEs) during the trial.
Assess and rate severity of AEs during the conduct of the protocol as delegated.
Primary Investigator responsibility in PIs absence, as delegated.
Educate study team on patient population and mechanism of action of the study medication / device.
Adhere to requirements on the FDA1572, Statement of Investigator form.
Collaborate with site leadership to ensure operational goals are met.
Possess through understanding of clinical research protocols and patient populations for each clinical research trial.
Develop and maintain strong working knowledge of regulatory requirements and GCP standards.
Ensure appropriate delegation and training of the Clinical team.
Complete training as required per sponsor’s vendors to obtain certification to conduct testing and rating scales for specific protocols.
Attend Investigator meetings and educational seminars.
Other duties as assigned

Desired Skills and Qualifications:

At least 3 years experience conducting clinical research trials as either PI or Sub-I.
Possess and maintain a valid MD or DO medical license, PA, or NP license.
Active license to practice medicine within the state.
Understanding of FDA regulations, ICH guidelines, and Good Clinical Practices.
Exercise Standard Universal Precautions
Demonstrate strong leadership skills.
Excellent task management and prioritization skills.
Strong verbal and written skills
Great interpersonal skills
Keen and acute attention to detail
Ability to work independently and demonstrate initiative.
Positive, collaborative, and team oriented.
Ability to work in a fast-paced environment, adapt, and ability to multi-task.
Excellent follow-up skills.
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.

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AMR jobs

Sub-Investigator - Nurse Practitioner/Physician Assistant

Senior CRC

Research Assistant - Medical Assistant

Research Assistant

Data Management Specialist

Clinical Research Coordinator 1

Chief Operating Officer

Research Assistant - Medical Lab Technician (Night Shift)

HR Manager

Budget Specialist

Regulatory Manager

Senior Project Management

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