Top 995 Irb Manager Jobs

Senior CRC
AMR Clinical —Myrtle Beach, SC
- Overtime
- Vital signs
- English
- 3 years
- Flexible schedule
Quick Apply
Clinical Trial Manager
Confidential —Bellevue, WA
- $90,000 - $120,000 a year
- Full-time
- Background check
- Medicine
- Doctoral degree
- Health insurance
- Dental insurance
Quick Apply
Clinical Research Manager
Chemidox Clinical Trials —Lancaster, CA
- Full-time
- 7 years
- PMP
- HIPAA
- Paid holidays
- Health insurance
Quick Apply
1d
Director Of Outpatient Quality, Network Administration, Full-Time, Days
MarinHealth Medical Network —Novato, CA
- $182,728 - $219,273 a year
- 8 hour shift
- Nursing
- RN License
- Analysis skills
Quick Apply
Director, Clinical Operations - AAV
Rocket Pharmaceuticals —Cranbury, NJ
- $196,000 - $294,000 a year
- Full-time
- Microsoft Outlook
- 8 years
- Bachelor's degree
- Paid holidays
- Health insurance
Manager High Fidelity and Procedural Simulation, Simulation Center
UT Southwestern —Dallas, TX
- Full-time
- 5 years
- Master's degree
- Analysis skills
- Paid parental leave
- Paid holidays
11d
Senior Manager, Global Clinical Scientist (Cell Therapy)
BMS —Brisbane, CA
- $150,770 - $210,110 a year
- Email
- Hybrid work
- Microsoft Word
- Medicine
- Microsoft Excel
- Paid holidays
- Disability insurance
Principal Clinical Trial Manager
TransMedics, Inc. —Andover, MA
- $137,100 - $193,700 a year
- Full-time
- Bachelor of Science
- Office
- Master's degree
- Employee stock purchase plan
- Disability insurance
Quick Apply
5d
Registered Nurse - Clinical Research Coordinator- RN
Wichita Urology Group —Wichita, KS
- Full-time
- Nursing
- RN License
- Laboratory experience
- Health savings account
- Health insurance
Quick Apply
Clinical Research Coordinator III
Vanderbilt University Medical Center —Nashville, TN
- Full-time
- Hybrid work
- Spanish
- Bachelor's degree
- Continuous improvement
- Health insurance
Operations Manager Clinical Trials
CAREERXCHANGE —Miami, FL
- $41 - $56 an hour
- Temporary
- Nursing
- Management
- 5 years
Quick Apply
Associate Director, Pediatric Clinical Research - Cancer Institute
Nicklaus Children's Hospital —Miami, FL
- Medicine
- 8 years
- Doctor of Philosophy
Regulatory Coordinator
CenExel Clinical Research —Hollywood, FL
- Overtime
- Background check
- Microsoft Excel
- Psychiatry
- Health savings account
- Health insurance
Quick Apply
Region Manager
Care Access —Boston, MA
- $95,000 - $115,000 a year
- Up to 50% travel
- Inventory management
- Pass drug screening
- Health savings account
- Paid holidays
Quality Assurance Coordinator (Clinical Research)
Research Centers of America —Hollywood, FL
- Full-time
- Background check
- Spanish
- Psychiatry
- Health savings account
- Health insurance
Quick Apply
Nurse Manager Inpatient Obstetrics
Clinical Management Consultants —West Haverstraw, NY
- $133,670 - $155,770 a year
- Full-time
- Nursing
- Inpatient
- Ob/Gyn
- Health insurance
- Dental insurance
SP Program Manager - 537528
FLORIDA INTERNATIONAL UNIVERSITY —Miami, FL
- Master's degree
- University
- Bachelor's degree
12d
Registered Nurse (RN) — Clinical Research Nurse Coordinator — Liver Institute of Virginia at St. Mary's Hospital
Bon Secours —Richmond, VA
- $36.42 - $58.28 an hour
- Nursing
- Patient monitoring
- RN License
- Health savings account
- Disability insurance
Nurse Scientist
Houston Methodist The Woodlands Hospital —The Woodlands, TX
- Full-time
- Acute care
- Nursing
- Doctoral degree
Associate Customer Success Manager
REALTIME SOFTWARE SOLUTIONS LLC —Remote
- Full-time
- Remote
- HIPAA
- Mid-level
- Bachelor's degree
- Paid parental leave
- Paid holidays
Quick Apply

I want to receive the latest job alert for Irb Manager

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

Irb Manager jobs near

Customer Success Manager jobs in Remote

Senior Clinical Research Coordinator jobs in Nashville, TN

Director Of Operations jobs in Cranbury, NJ

Program Manager jobs in Miami, FL

Clinical Trial Manager jobs in Miami, FL

Center Manager jobs in Dallas, TX

Clinical Trial Manager jobs in Andover, MA

Associate Director jobs in Miami, FL

Regional Manager jobs in Boston, MA

Scientist jobs in The Woodlands, TX

Clinical Research Coordinator jobs in Wichita, KS

Data Scientist jobs in Philadelphia, PA

Senior Scientist jobs in Nashville, TN

Senior Living jobs in Denver, CO

Senior Scientist jobs in Research Triangle Park, NC

Senior Scientist jobs in Avenel, NJ

Senior Scientist jobs in New York, NY

Data Scientist jobs in Pittsburgh, PA

Customer Success Manager jobs in Atlanta, GA

Customer Success Manager jobs in Burlington, MA

Senior CRC

AMR Clinical -
Myrtle Beach, SC

Quick Apply

Job Details

Full-time

Benefits

Flexible schedule

Qualifications

Quality control corrective actions
Laboratory sample storage
Project team coordination
Document compliance management
Vital signs
Clinical compliance checks
Informed consent
Team supervision
Phone communication
Pre-examination patient preparation
Adverse event reporting
Clinical trial risk management
Patient transfer methods
Preventive action implementation
Client rapport building
Assisting with diagnostic tests and procedures
Patient weighing scales
Quality control preventive actions
Corrective and preventive actions (CAPA)
English
Phlebotomy specimen handling
Risk mitigation strategy implementation
Incident Escalation
ECG equipment
3 years
Healthcare practice inventory management
Medical diagnostic testing
Team development
Clinical staff training
One-on-one patient counseling

Full Job Description

The Clinical Research Coordinator will perform and manage tasks that are critical to clinical research studies. The Clinical Research Coordinator must ensure compliance with federal regulations, study protocol guidelines, as well as monitor study participants, and take a proactive approach to identify issues on an ongoing basis throughout the clinical research study.

To consistently embody AMR Clinical’s Core Values:

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

The Clinical Research Coordinator reports to the Site Manager/Team Lead.

Classification: Non-Exempt

Primary Responsibilities:

Expanded role in team management, mentorship, and training, which includes over-sight of level 1 CRC’s, Research Assistants and ancillary staff.
Advanced Problem Solving & Decision-Making. Takes ownership of identifying, analyzing, and resolving complex study-related challenges, including protocol deviations, regulatory compliance issues, and operational inefficiencies. Proactively collaborates with QA and Site Manager to develop and implement corrective and preventive action plans to mitigate risks and improve study outcomes. Serves as a key resource for junior staff, providing guidance and training on problem-solving strategies while escalating critical issues to leadership as needed.
Advanced knowledge of protocol and procedures.

Greater responsibility for regulatory compliance, protocol deviations, and audits.
Deeper involvement in recruitment strategy and study performance.

Higher engagement with study sponsors, CROs, monitors/CRA’s, IRBs, laboratories, and clinical personnel within the research industry.
Coordinate clinical trials per FDA requirements and GCP Guidelines per sponsor protocols.
Establish understanding of SOP’s and implement the SOP’s
Gain understanding of the pharmaceutical drug per clinical trial.

Advanced skills in study start-up and close-out procedures.
Manage complex clinical trials, including those with challenging study designs and special patient populations.
Work closely with Investigators to optimize site performance, improve study compliance, and facilitate better communication between research staff and investigators.

Notify the correct personnel of any adverse events per the study protocol (PI, Sub-I, monitor/CRA, etc.)
Be the study ambassador on assigned studies to advise team members on protocols and procedures to ensure successful implementation and completion of the clinical research study.
Establish and maintain patient rapport.
Clinical data collection (vital signs, EKG recording, weight, height, etc.)
Obtain medical records and review as required.
Phlebotomy
Specimen collection, processing, and storage
Transporting clinical specimens to laboratory.
Educate subjects on diaries and oversees compliance with diary completion.
Provides subjects instructions per study (diaries, restricted meds, study reminders, etc.)
Responsible for completing patient phone call visits in accordance to the standard protocol period.
Ensure documentation follows ALCOA standards and is completed in a timely manner.
Ensure all necessary documents are completed, signed and dated.

Provides required information to Contract Research Organization (CRO), Institutional Review Board (IRB), sponsoring organization, Food and Drug Administration (FDA), and/or other appropriate agency as required.
Manage study inventory and order supplies as needed.
Prepare and assist study monitors during onsite visits.

Maintain familiarity with all ongoing clinical research studies.
Travel to Investigator meetings as needed.
Promote team mentality by working flexible hours as needed and completing tasks outside the scope of everyday duties
Mentor team members to promote professional development
Position may require occasional weekend and/or overtime hours.
Other duties as assigned

Desired Skills and Qualifications:

3+ years of experience in clinical research.
Completion of formal medical training, educational program, or healthcare experience
Strong medical terminology
Ability to perform clinical, laboratory, and diagnostic tests (vital signs, height, weight, temperature, etc.).
Ability to work independently and lead study-related tasks.
Ability to multi-task in a high-paced evolving environment.
Exceptional listening, written, and verbal communication skills as well.
Demonstrate proficiency in office equipment and software programs.
Excellent organizational and task management skills.
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

Irb Manager jobs

Senior CRC

Clinical Trial Manager

Clinical Research Manager

Director Of Outpatient Quality, Network Administration, Full-Time, Days

Director, Clinical Operations - AAV

Manager High Fidelity and Procedural Simulation, Simulation Center

Senior Manager, Global Clinical Scientist (Cell Therapy)

Principal Clinical Trial Manager

Registered Nurse - Clinical Research Coordinator- RN

Clinical Research Coordinator III

Operations Manager Clinical Trials

Associate Director, Pediatric Clinical Research - Cancer Institute

Regulatory Coordinator

Region Manager

Quality Assurance Coordinator (Clinical Research)

Nurse Manager Inpatient Obstetrics

SP Program Manager - 537528

Registered Nurse (RN) — Clinical Research Nurse Coordinator — Liver Institute of Virginia at St. Mary's Hospital

Nurse Scientist

Associate Customer Success Manager

I want to receive the latest job alert for Irb Manager

Related Searches

Explore jobs in more locations

Job Seeker Tools

Employer Tools

Browse

Stay Connected