This is a remote position. The Participant Recruitment Analyst will be responsible for analyzing ... Maintain compliance with HIPAA, FDA, GCP, IRB guidelines, and M3 Wake Research SOPs * Review ...
This is a remote position. The Participant Recruitment Analyst will be responsible for analyzing ... Maintain compliance with HIPAA, FDA, GCP, IRB guidelines, and M3 Wake Research SOPs * Review ...
This is a remote position. The Participant Recruitment Analyst will be responsible for analyzing ... Maintain compliance with HIPAA, FDA, GCP, IRB guidelines, and M3 Wake Research SOPs * Review ...
This is a remote position. The Participant Recruitment Analyst will be responsible for analyzing ... Maintain compliance with HIPAA, FDA, GCP, IRB guidelines, and M3 Wake Research SOPs * Review ...
Participant Recruitment Analyst
Raleigh, NC ยท On-site +1
This is a remote position. The Participant Recruitment Analyst will be responsible for analyzing ... Maintain compliance with HIPAA, FDA, GCP, IRB guidelines, and M3 Wake Research SOPs * Review ...
Participant Recruitment Analyst
Raleigh, NC ยท On-site +1
This is a remote position. The Participant Recruitment Analyst will be responsible for analyzing ... Maintain compliance with HIPAA, FDA, GCP, IRB guidelines, and M3 Wake Research SOPs * Review ...
Sr. Clinical Research Associate
Durham, NC ยท On-site +1
Conduct remote monitoring activities appropriate for observational studies, including review of ... Support IRB submissions, protocol amendments, and regulatory documentation to ensure ongoing ...
Sr. Clinical Research Associate
Durham, NC ยท On-site +1
Conduct remote monitoring activities appropriate for observational studies, including review of ... Support IRB submissions, protocol amendments, and regulatory documentation to ensure ongoing ...
Performing on-site and remote monitoring visits in accordance with protocol, GCP, ICH guidelines, and company SOPs * Building strong relationships with investigative sites and serving as a trusted ...
Performing on-site and remote monitoring visits in accordance with protocol, GCP, ICH guidelines, and company SOPs * Building strong relationships with investigative sites and serving as a trusted ...
Performing on-site and remote monitoring visits in accordance with protocol, GCP, ICH guidelines, and company SOPs * Building strong relationships with investigative sites and serving as a trusted ...
Performing on-site and remote monitoring visits in accordance with protocol, GCP, ICH guidelines, and company SOPs * Building strong relationships with investigative sites and serving as a trusted ...
Performing on-site and remote monitoring visits in accordance with protocol, GCP, ICH guidelines, and company SOPs * Building strong relationships with investigative sites and serving as a trusted ...
Performing on-site and remote monitoring visits in accordance with protocol, GCP, ICH guidelines, and company SOPs * Building strong relationships with investigative sites and serving as a trusted ...
On-site and virtual/remote monitoring activities with a risk-based monitoring approach (including centralized data review) through our integrated Clinical Trial Management System to identify site ...
On-site and virtual/remote monitoring activities with a risk-based monitoring approach (including centralized data review) through our integrated Clinical Trial Management System to identify site ...
Willingness to travel as required (approximately 60%) #LI-LB1 #LI-REMOTE Employment with ICON is contingent upon having the legal right to work in the country where the role is based. Rewards ...
Quick apply
Willingness to travel as required (approximately 60%) #LI-LB1 #LI-REMOTE Employment with ICON is contingent upon having the legal right to work in the country where the role is based. Rewards ...
Clinical Research Associate II
Cary, NC ยท Remote
Willingness to travel as required (approximately 60%) #LI-LB1 #LI-REMOTE Employment with ICON is contingent upon having the legal right to work in the country where the role is based. Rewards ...
Clinical Research Associate II
Cary, NC ยท Remote
Willingness to travel as required (approximately 60%) #LI-LB1 #LI-REMOTE Employment with ICON is contingent upon having the legal right to work in the country where the role is based. Rewards ...
Willingness to travel as required (approximately 60%) #LI-LB1 #LI-REMOTE Employment with ICON is contingent upon having the legal right to work in the country where the role is based. Rewards ...
Willingness to travel as required (approximately 60%) #LI-LB1 #LI-REMOTE Employment with ICON is contingent upon having the legal right to work in the country where the role is based. Rewards ...
Clinical Research Associate II
Cary, NC ยท Remote
Willingness to travel as required (approximately 60%) #LI-LB1 #LI-REMOTE Employment with ICON is contingent upon having the legal right to work in the country where the role is based. Rewards ...
Quick apply
Clinical Research Associate II
Cary, NC ยท Remote
Willingness to travel as required (approximately 60%) #LI-LB1 #LI-REMOTE Employment with ICON is contingent upon having the legal right to work in the country where the role is based. Rewards ...
Willingness to travel as required (approximately 60%) #LI-LB1 #LI-REMOTE Employment with ICON is contingent upon having the legal right to work in the country where the role is based. Rewards ...
Quick apply
Willingness to travel as required (approximately 60%) #LI-LB1 #LI-REMOTE Employment with ICON is contingent upon having the legal right to work in the country where the role is based. Rewards ...
Willingness to travel as required (approximately 60%) #LI-LB1 #LI-REMOTE Employment with ICON is contingent upon having the legal right to work in the country where the role is based. Rewards ...
Willingness to travel as required (approximately 60%) #LI-LB1 #LI-REMOTE Employment with ICON is contingent upon having the legal right to work in the country where the role is based. Rewards ...
North America | Remote | Sponsor-Dedicated (FSP) Opportunities ICON is a global healthcare intelligence and clinical research organisation united by a mission to bring new medicines and treatments to ...
Quick apply
North America | Remote | Sponsor-Dedicated (FSP) Opportunities ICON is a global healthcare intelligence and clinical research organisation united by a mission to bring new medicines and treatments to ...
FSP Sr. Clinical Research Associate II - NYC Metro or PHL - Onc
Durham, NC ยท Remote
$125 - $140K/hr
Target Pay Range: $125 - $140K #LI - Remote Applications will be accepted on an ongoing basis. Learn more about our EEO & Accommodations request here.
FSP Sr. Clinical Research Associate II - NYC Metro or PHL - Onc
Durham, NC ยท Remote
$125 - $140K/hr
Target Pay Range: $125 - $140K #LI - Remote Applications will be accepted on an ongoing basis. Learn more about our EEO & Accommodations request here.
Clinical Research Associate II/III - US
Durham, NC ยท On-site +1
Remote Who we are? Optimapharm is a mid-sized, global Contract Research Organisation (CRO) turning science into hope through agile, patient-focused clinical development. We specialise in Phase I-IV ...
Clinical Research Associate II/III - US
Durham, NC ยท On-site +1
Remote Who we are? Optimapharm is a mid-sized, global Contract Research Organisation (CRO) turning science into hope through agile, patient-focused clinical development. We specialise in Phase I-IV ...
Clinical Research Coordinator - Raleigh, NC
Raleigh, NC ยท Remote
$35 - $42/hr
This position is not eligible for employment sponsorship. #LI-CES and #LI-DNP #LI-HCP #remote IQVIA is a leading global provider of clinical research services, commercial insights and healthcare ...
Clinical Research Coordinator - Raleigh, NC
Raleigh, NC ยท Remote
$35 - $42/hr
This position is not eligible for employment sponsorship. #LI-CES and #LI-DNP #LI-HCP #remote IQVIA is a leading global provider of clinical research services, commercial insights and healthcare ...
Clinical Research Coordinator
Raleigh, NC ยท Remote
$35 - $42/hr
This position is not eligible for employment sponsorship. #LI-CES and #LI-DNP #LI-HCP #remote IQVIA is a leading global provider of clinical research services, commercial insights and healthcare ...
Clinical Research Coordinator
Raleigh, NC ยท Remote
$35 - $42/hr
This position is not eligible for employment sponsorship. #LI-CES and #LI-DNP #LI-HCP #remote IQVIA is a leading global provider of clinical research services, commercial insights and healthcare ...
Clinical Research Associate II/III - US
Raleigh, NC ยท On-site +1
Remote Who we are? Optimapharm is a mid-sized, global Contract Research Organisation (CRO) turning science into hope through agile, patient-focused clinical development. We specialise in Phase I-IV ...
Clinical Research Associate II/III - US
Raleigh, NC ยท On-site +1
Remote Who we are? Optimapharm is a mid-sized, global Contract Research Organisation (CRO) turning science into hope through agile, patient-focused clinical development. We specialise in Phase I-IV ...
Remote Irb information
See Raleigh, NC salary details
$16.82 - $17.40
7% of jobs
$17.95 is the 25th percentile. Wages below this are outliers.
$17.40 - $17.97
19% of jobs
$17.97 - $18.55
5% of jobs
$18.55 - $19.12
3% of jobs
$19.12 - $19.69
14% of jobs
The median wage is $19.84 / hr.
$19.69 - $20.27
6% of jobs
$20.27 - $20.84
0% of jobs
$20.84 - $21.41
0% of jobs
$21.41 - $21.99
0% of jobs
$22.44 is the 75th percentile. Wages above this are outliers.
$21.99 - $22.56
26% of jobs
$22.56 - $23.13
20% of jobs
$16
$20
$23
How much do remote irb jobs pay per hour?
What is a remote IRB?
What is a remote IRB job?
Remote IRB jobs include work as a remote IRB administrator, a remote IRB analyst, and a remote IRB coordinator. Your responsibilities and duties differ depending on your specific position. For example, a remote IRB analyst performs analysis and is responsible for assessing whether or not a study meets all the guidelines and regulatory requirements for the safety and welfare of human subjects. As a remote IRB coordinator, your role is to coordinate internal review board research and compliance during studies. This includes ensuring that test subjects received the proper paperwork and release forms and that studies remain on schedule. You can work from home in any of these positions.
What are the key skills and qualifications needed to thrive as a remote IRB coordinator, and why are they important?
What are some common challenges faced by remote IRB coordinators, and how can they be addressed?
What is the difference between Remote Irb vs Remote Clinical Research Coordinator?
| Aspect | Remote Irb | Remote Clinical Research Coordinator |
|---|---|---|
| Required Credentials | IRB approval, research ethics knowledge | Clinical research experience, regulatory knowledge |
| Work Environment | Review boards, ethics committees, administrative | Study sites, patient interaction, data management |
| Employer & Industry Usage | Hospitals, research institutions, biotech firms | Pharmaceutical companies, CROs, hospitals |
| Common Search & Comparison | Yes | No |
The Remote Irb role focuses on reviewing research protocols for ethical compliance, requiring knowledge of research ethics and IRB procedures. In contrast, a Remote Clinical Research Coordinator manages study operations, patient recruitment, and data collection. While both roles are integral to clinical research, they differ in responsibilities, credentials, and work environment.
What are the most commonly searched types of Irb jobs in Raleigh, NC?
The most popular types of Irb jobs in Raleigh, NC are:
What are popular job titles related to Remote Irb jobs in Raleigh, NC?
For Remote Irb jobs in Raleigh, NC, the most frequently searched job titles are:
What job categories do people searching Remote Irb jobs in Raleigh, NC look for?
The top searched job categories for Remote Irb jobs in Raleigh, NC are:
What cities near Raleigh, NC are hiring for Remote Irb jobs?
Cities near Raleigh, NC with the most Remote Irb job openings:

Full-time
Medical, Dental, Vision, Life, Retirement, PTO
This job post hasย expired 1 day ago.ย Applications are no longer accepted.
Job description
M3 Wake Research, an M3USA Company, is an integrated network of premier investigational sites meeting the clinical research needs of global biopharmaceutical, biotechnology, medical device, pharmaceutical and clinical research organizations (CROs). With close to 30 owned and managed research sites across the country, M3 Wake Research is one of the largest independent, multi-site clinical research companies in the US. M3 Wake Research continues to grow through acquisitions and uncompromising commitment to careful planning and execution in accordance with regulatory compliance.
Conducting studies since 1984, M3 Wake Research owns a proprietary patient database of potential clinical trial participants across the US. As of today, our board-certified physicians have completed more than 7,000+ successful clinical trials, while consistently exceeding sponsor expectations for integrity, timeliness, subject enrollment, human protection, and expeditious delivery of accurate evaluable data.
Due to our continued growth, we are hiring a Participant Recruitment Analyst at Wake Research, an M3 company. This is a remote position.
Job DescriptionThe Participant Recruitment Analyst will be responsible for analyzing and reviewing medical records to evaluate potential outreach and recruitment opportunities for upcoming clinical trials at M3 Wake Research. The ideal candidate will have a strong understanding of medical record documentation requirements and coding guidelines.
Essential Duties and Responsibilities:
Including, but not limited to the following:
- Review electronic and paper medical records to assess trial eligibility and generate qualified leads
- Conduct pre-screening interviews and screening calls to determine participant eligibility and schedule onsite visits
- Perform medical record abstraction and data collection activities
- Use electronic recruitment workflows to track enrollment, maintain study records, and coordinate across research sites
- Track project statuses and report enrollment metrics
- Maintain compliance with HIPAA, FDA, GCP, IRB guidelines, and M3 Wake Research SOPs
- Review clinical trial protocols, inclusion/exclusion criteria, and study requirements
- Collaborate with Clinical Affairs on community partner communications and recruitment support
- Attend team meetings and participate in community outreach efforts as assigned
- Maintain regular attendance, participate in video conferences with camera on, and comply with Company policies
- Maintain confidentiality of protected health information (PHI)
- A minimum of 2 years of clinical research experience at a clinical research site, CRO, Sponsor, or participant recruitment vendor.
- Bachelor's Degree in a job-related field, or a combination of academic, professional, or work experience that demonstrates ability to perform the duties of the position.
- Experience with medical record data abstraction into a proprietary medical record review data collection application.
- MA, EMT, LVN/LPN, or RN certification or licensure, or similar certification, preferred.
- Basic knowledge of medical terminology.
Additional Information
About M3USA
M3 USA is at the forefront of healthcare innovation, offering digital solutions across healthcare, life sciences, pharmaceuticals, and more. Since our inception in 2000, we’ve seen remarkable growth, fueled by our mission to utilize the internet for a healthier world and more efficient healthcare systems.
Our success is anchored in our trusted digital platforms that engage physician communities globally, facilitating impactful medical education, precise job placement, and insightful market research. M3 USA prides itself on a dynamic and innovative work environment where every team member contributes to global health advancements.
Joining M3 USA means being part of a dedicated team striving to make a significant difference in healthcare. We provide a unique opportunity for you to be at the cutting edge of healthcare innovation, shaping the future in a meaningful career. Embrace the chance to drive change with M3 USA.
Benefits:
A career opportunity with M3 Wake Research offers competitive wages, and benefits such as:
- 401(k), 401(k) matching
- Dental insurance
- Disability insurance
- Employee assistance program
- Flexible spending account
- Health insurance
- Life insurance
- Paid time off
- Vision insurance
*M3 reserves the right to change this job description to meet the business needs of the organization
#LI-Remote
#LI-LB1
About Wake Research
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