Clinical Trial Lead
Cary, NC · On-site +1
We are looking for a Clinical Trial Leader (CTL) to join our A-team (office-based*/remote). As a ... Supporting the management team with training, process improvements, co-monitoring visits, mentoring ...
Clinical Trial Lead
Cary, NC · On-site +1
We are looking for a Clinical Trial Leader (CTL) to join our A-team (office-based*/remote). As a ... Supporting the management team with training, process improvements, co-monitoring visits, mentoring ...
Clinical Trial Lead
Cary, NC · Remote
We are looking for a Clinical Trial Leader (CTL) to join our A-team (office-based*/remote). As a ... Supporting the management team with training, process improvements, co-monitoring visits ...
Quick apply
Clinical Trial Lead
Cary, NC · Remote
We are looking for a Clinical Trial Leader (CTL) to join our A-team (office-based*/remote). As a ... Supporting the management team with training, process improvements, co-monitoring visits ...
Clinical Trial Lead
Cary, NC · On-site +1
We are looking for a Clinical Trial Leader (CTL) to join our A-team (office-based*/remote). As a ... Supporting the management team with training, process improvements, co-monitoring visits,mentoring ...
Clinical Trial Lead
Cary, NC · On-site +1
We are looking for a Clinical Trial Leader (CTL) to join our A-team (office-based*/remote). As a ... Supporting the management team with training, process improvements, co-monitoring visits,mentoring ...
Clinical Trial Rater
Durham, NC · Remote
Remote based in the US Hours: Approximately 5h per week Role: Clinical Specialist Start: immediate ... Education: PhD or PsyD (Psychology, Psychiatry, Health Sciences), Medical Doctor (MD), Foreign ...
Clinical Trial Rater
Durham, NC · Remote
Remote based in the US Hours: Approximately 5h per week Role: Clinical Specialist Start: immediate ... Education: PhD or PsyD (Psychology, Psychiatry, Health Sciences), Medical Doctor (MD), Foreign ...
Clinical Trial Rater
Raleigh, NC · Remote
Remote based in the US Hours: Approximately 5h per week Role: Clinical Specialist Start: immediate ... Education: PhD or PsyD (Psychology, Psychiatry, Health Sciences), Medical Doctor (MD), Foreign ...
Clinical Trial Rater
Raleigh, NC · Remote
Remote based in the US Hours: Approximately 5h per week Role: Clinical Specialist Start: immediate ... Education: PhD or PsyD (Psychology, Psychiatry, Health Sciences), Medical Doctor (MD), Foreign ...
Clinical Trial Project Manager
Morrisville, NC · On-site +1
... monitoring, site management, data management, pharmacovigilance, regulatory, IP supply, and medical ... LI-remote We may use artificial intelligence (AI) tools to support parts of the hiring process ...
Clinical Trial Project Manager
Morrisville, NC · On-site +1
... monitoring, site management, data management, pharmacovigilance, regulatory, IP supply, and medical ... LI-remote We may use artificial intelligence (AI) tools to support parts of the hiring process ...
Clinical Trial Lead
Durham, NC · On-site +1
Provide strategic input and make scientific or medical decisions in early clinical development, in ... Monitor and guide financial aspects of trials including scope, budget, schedule, and change control.
Clinical Trial Lead
Durham, NC · On-site +1
Provide strategic input and make scientific or medical decisions in early clinical development, in ... Monitor and guide financial aspects of trials including scope, budget, schedule, and change control.
Clinical Trial Lead
Durham, NC · On-site +1
Provide strategic input and make scientific or medical decisions in early clinical development, in ... Monitor and guide financial aspects of trials including scope, budget, schedule, and change control.
Clinical Trial Lead
Durham, NC · On-site +1
Provide strategic input and make scientific or medical decisions in early clinical development, in ... Monitor and guide financial aspects of trials including scope, budget, schedule, and change control.
Remote based in the US Hours: Approximately 5h per week Role: Clinical Specialist Start: immediate ... Education: PhD or PsyD (Psychology, Psychiatry, Health Sciences), Medical Doctor (MD), Foreign ...
Remote based in the US Hours: Approximately 5h per week Role: Clinical Specialist Start: immediate ... Education: PhD or PsyD (Psychology, Psychiatry, Health Sciences), Medical Doctor (MD), Foreign ...
Remote based in the US Hours: Approximately 5h per week Role: Clinical Specialist Start: immediate ... Education: PhD or PsyD (Psychology, Psychiatry, Health Sciences), Medical Doctor (MD), Foreign ...
Remote based in the US Hours: Approximately 5h per week Role: Clinical Specialist Start: immediate ... Education: PhD or PsyD (Psychology, Psychiatry, Health Sciences), Medical Doctor (MD), Foreign ...
Remote US or Canadian based. We are seeking candidates with either CAR T or Ophthalmology ... Proactive planning for monitoring activities to ensure data integrity, patient safety and endpoint ...
Remote US or Canadian based. We are seeking candidates with either CAR T or Ophthalmology ... Proactive planning for monitoring activities to ensure data integrity, patient safety and endpoint ...
Clinical Trials Manager- Remote
Chapel Hill, NC · Remote
$62 - $64.73/hr
... trial requirements . * Experience with clinical monitoring practices and study operations ... include medical, dental, vision, life insurance, short-term disability, additional voluntary ...
Quick apply
Clinical Trials Manager- Remote
Chapel Hill, NC · Remote
$62 - $64.73/hr
... trial requirements . * Experience with clinical monitoring practices and study operations ... include medical, dental, vision, life insurance, short-term disability, additional voluntary ...
Sr. Medical Director, Rheumatology - US Remote
Durham, NC · Remote
$240K - $340K/yr
Senior Medical Director, Rheumatology - US Remote Based Raising CRO standards for innovation and ... monitoring experience or other relevant clinical development/trial experience at a CRO ...
Sr. Medical Director, Rheumatology - US Remote
Durham, NC · Remote
$240K - $340K/yr
Senior Medical Director, Rheumatology - US Remote Based Raising CRO standards for innovation and ... monitoring experience or other relevant clinical development/trial experience at a CRO ...
Monitoring clinical trial sites to ensure adherence to study protocols, regulatory requirements ... Willingness to travel as required (approximately 60%) #LI-LB1 #LI-REMOTE Employment with ICON is ...
Monitoring clinical trial sites to ensure adherence to study protocols, regulatory requirements ... Willingness to travel as required (approximately 60%) #LI-LB1 #LI-REMOTE Employment with ICON is ...
Monitoring clinical trial sites to ensure adherence to study protocols, regulatory requirements ... Willingness to travel as required (approximately 60%) #LI-LB1 #LI-REMOTE Employment with ICON is ...
Quick apply
Monitoring clinical trial sites to ensure adherence to study protocols, regulatory requirements ... Willingness to travel as required (approximately 60%) #LI-LB1 #LI-REMOTE Employment with ICON is ...
Monitoring clinical trial sites to ensure adherence to study protocols, regulatory requirements ... Willingness to travel as required (approximately 60%) #LI-LB1 #LI-REMOTE Employment with ICON is ...
Quick apply
Monitoring clinical trial sites to ensure adherence to study protocols, regulatory requirements ... Willingness to travel as required (approximately 60%) #LI-LB1 #LI-REMOTE Employment with ICON is ...
Monitoring clinical trial sites to ensure adherence to study protocols, regulatory requirements ... Willingness to travel as required (approximately 60%) #LI-LB1 #LI-REMOTE Employment with ICON is ...
Monitoring clinical trial sites to ensure adherence to study protocols, regulatory requirements ... Willingness to travel as required (approximately 60%) #LI-LB1 #LI-REMOTE Employment with ICON is ...
Monitoring clinical trial sites to ensure adherence to study protocols, regulatory requirements ... Willingness to travel as required (approximately 60%) #LI-LB1 #LI-REMOTE Employment with ICON is ...
Quick apply
Monitoring clinical trial sites to ensure adherence to study protocols, regulatory requirements ... Willingness to travel as required (approximately 60%) #LI-LB1 #LI-REMOTE Employment with ICON is ...
Monitoring clinical trial sites to ensure adherence to study protocols, regulatory requirements ... Willingness to travel as required (approximately 60%) #LI-LB1 #LI-REMOTE Employment with ICON is ...
Monitoring clinical trial sites to ensure adherence to study protocols, regulatory requirements ... Willingness to travel as required (approximately 60%) #LI-LB1 #LI-REMOTE Employment with ICON is ...
Senior Clinical Research Associate
Raleigh, NC · On-site +1
Conduct on-site and remote visits/contacts, including Qualification, Initiation, Monitoring ... Address and resolve issues at clinical trial sites, including the need for additional training ...
Senior Clinical Research Associate
Raleigh, NC · On-site +1
Conduct on-site and remote visits/contacts, including Qualification, Initiation, Monitoring ... Address and resolve issues at clinical trial sites, including the need for additional training ...
Remote Medical Monitor Clinical Trial information
See Raleigh, NC salary details
$16.82 - $21.50
4% of jobs
$21.50 - $26.17
8% of jobs
$26.17 - $30.84
12% of jobs
$30.99 is the 25th percentile. Wages below this are outliers.
$30.84 - $35.52
26% of jobs
$35.52 - $40.19
18% of jobs
$41.81 is the 75th percentile. Wages above this are outliers.
$40.19 - $44.87
19% of jobs
$44.87 - $49.54
6% of jobs
$49.54 - $54.21
2% of jobs
$54.21 - $58.89
1% of jobs
$58.89 - $63.56
1% of jobs
$63.56 - $68.23
2% of jobs
$16
$38
$68
How much do remote medical monitor clinical trial jobs pay per hour?
As of Sep 1, 2026, the average hourly pay for remote medical monitor clinical trial in Raleigh, NC is $38.87, according to ZipRecruiter salary data. Most workers in this role earn between $31.30 and $42.74 per hour, depending on experience, location, and employer.
What is the difference between Remote Medical Monitor Clinical Trial vs Remote Clinical Research Coordinator?
| Aspect | Remote Medical Monitor Clinical Trial | Remote Clinical Research Coordinator |
|---|---|---|
| Credentials | Medical degree or clinical background, certifications like CCRP or CCRA often preferred | Bachelor's degree, often in health or science fields; certifications like CCRP beneficial |
| Work Environment | Primarily remote, overseeing trial safety and compliance | Remote or on-site, managing study logistics and participant coordination |
| Employer & Industry Usage | Pharmaceutical companies, CROs, biotech firms | Research institutions, hospitals, CROs |
The Remote Medical Monitor Clinical Trial focuses on overseeing patient safety and trial compliance remotely, often requiring clinical credentials. In contrast, the Remote Clinical Research Coordinator manages study logistics and participant coordination, with a broader range of educational backgrounds. Both roles are essential in clinical research but differ in responsibilities and required qualifications.
What are the most commonly searched types of Medical Monitor Clinical Trial jobs in Raleigh, NC?
The most popular types of Medical Monitor Clinical Trial jobs in Raleigh, NC are:
What are popular job titles related to Remote Medical Monitor Clinical Trial jobs in Raleigh, NC?
For Remote Medical Monitor Clinical Trial jobs in Raleigh, NC, the most frequently searched job titles are:
What job categories do people searching Remote Medical Monitor Clinical Trial jobs in Raleigh, NC look for?
The top searched job categories for Remote Medical Monitor Clinical Trial jobs in Raleigh, NC are:
What cities near Raleigh, NC are hiring for Remote Medical Monitor Clinical Trial jobs?
Cities near Raleigh, NC with the most Remote Medical Monitor Clinical Trial job openings:
Clinical Trial Lead
Cary, NC • On-site, Remote
Allucent
Full-time
Re-posted 18 days ago
Job description
At Allucent™, we are dedicated to helping small-medium biopharmaceutical companies efficiently navigate the complex world of clinical trials to bring life-changing therapies to patients in need across the globe.
We are looking for a Clinical Trial Leader (CTL) to join our A-team (office-based*/remote). As a CTL at Allucent, you are providing leadership, management and oversight to the Clinical Research Associates (CRAs) and other clinical functional groups, in their day-to-day clinical trial activities on a global, multi-country, or regional basis. The CTL is responsible for coordinating and managing the planning, implementation, tracking, and ensuring the clinical deliverables as per the trial contract, budget, timelines and with quality.
Responsibilities
As an expert in Clinical Trial Leadership, you are:
Requirements
To be successful you will possess:
Benefits
Benefits of working at Allucent include:
Disclaimers:
*Our office-based work policy encourages a dynamic work environment, prescribing a minimum of 2 days in office per week for employees within reasonable distance from one of our global offices.
"The Allucent Talent Acquisition team manages the recruitment and employment process for Allucent (US) LLC and its affiliates (collectively "Allucent"). Allucent does not accept unsolicited resumes from third-party recruiters or uninvited requests for collaboration on any of our open roles. Unsolicited resumes sent to Allucent employees will not obligate Allucent to the future employment of those individuals or potential remuneration to any third-party recruitment agency. Candidates should never be submitted directly to our hiring managers, employees, or human resources."
#LI-Remote #LI-Hybrid #LI-TCW
We are looking for a Clinical Trial Leader (CTL) to join our A-team (office-based*/remote). As a CTL at Allucent, you are providing leadership, management and oversight to the Clinical Research Associates (CRAs) and other clinical functional groups, in their day-to-day clinical trial activities on a global, multi-country, or regional basis. The CTL is responsible for coordinating and managing the planning, implementation, tracking, and ensuring the clinical deliverables as per the trial contract, budget, timelines and with quality.
Responsibilities
As an expert in Clinical Trial Leadership, you are:
- Coordinating and managing CRA activities across all geographies, liaising with sponsor and Project Manager and other functional leads to ensure clinical monitoring deliverables (timeline, budget, quality, productivity) are met.
- Liaising closely with the Project Manager (PM) and other department leaders if /when necessary, on all trial-related issues and service delivery.
- Supporting the management team with training, process improvements, co-monitoring visits, mentoring of staff and / or any other special assignments within Global Clinical Operations.
Requirements
To be successful you will possess:
- A degree in life sciences or nursing qualification preferred, but not required.
- A minimum of 5 years of clinical research experience with at least 2-years' CTL or other relevant experience.
- In-depth knowledge of ICH GCP, clinical trials and the critical elements for success in clinical trials
- Strong therapeutic background in oncology
- Possesses experience and knowledge in the CRO industry that will support Allucent's management of clinical trials
- Strong written and verbal communication skills including professional command of English language to communicate with internal and external stakeholders on a daily basis.
Benefits
Benefits of working at Allucent include:
- Comprehensive benefits package per location
- Competitive salaries per location
- Departmental Study/Training Budget for furthering professional development
- Flexible Working hours (within reason)
- Opportunity for remote/hybrid* working depending on location
- Leadership and mentoring opportunities
- Participation in our Buddy Program as a new or existing employee
- Internal growth opportunities and career progression
- Financially rewarding internal employee referral program
Disclaimers:
*Our office-based work policy encourages a dynamic work environment, prescribing a minimum of 2 days in office per week for employees within reasonable distance from one of our global offices.
"The Allucent Talent Acquisition team manages the recruitment and employment process for Allucent (US) LLC and its affiliates (collectively "Allucent"). Allucent does not accept unsolicited resumes from third-party recruiters or uninvited requests for collaboration on any of our open roles. Unsolicited resumes sent to Allucent employees will not obligate Allucent to the future employment of those individuals or potential remuneration to any third-party recruitment agency. Candidates should never be submitted directly to our hiring managers, employees, or human resources."
#LI-Remote #LI-Hybrid #LI-TCW