Maintain up-to-date knowledge of regulatory requirements related to clinical monitoring. * Assist in the development of clinical monitoring processes, standards, and training materials. * Performs ...
Maintain up-to-date knowledge of regulatory requirements related to clinical monitoring. * Assist in the development of clinical monitoring processes, standards, and training materials. * Performs ...
The Manager, Clinical Monitoring supports global and regional clinical trial operations (CTO) and ... assist CRAs to develop corrective and preventative actions to bring sites into compliance. * An ...
The Manager, Clinical Monitoring supports global and regional clinical trial operations (CTO) and ... assist CRAs to develop corrective and preventative actions to bring sites into compliance. * An ...
The Manager, Clinical Monitoring supports global and regional clinical trial operations (CTO) and ... assist CRAs to develop corrective and preventative actions to bring sites into compliance. * An ...
The Manager, Clinical Monitoring supports global and regional clinical trial operations (CTO) and ... assist CRAs to develop corrective and preventative actions to bring sites into compliance. * An ...
This role partners with Clinical Site Management Leadership to support monitoring excellence ... * Assist with review of monitoring trends and quality metrics to support consistency and ...
This role partners with Clinical Site Management Leadership to support monitoring excellence ... * Assist with review of monitoring trends and quality metrics to support consistency and ...
This role partners with Clinical Site Management Leadership to support monitoring excellence ... * Assist with review of monitoring trends and quality metrics to support consistency and ...
This role partners with Clinical Site Management Leadership to support monitoring excellence ... * Assist with review of monitoring trends and quality metrics to support consistency and ...
This role partners with Clinical Site Management Leadership to support monitoring excellence ... * Assist with review of monitoring trends and quality metrics to support consistency and ...
This role partners with Clinical Site Management Leadership to support monitoring excellence ... * Assist with review of monitoring trends and quality metrics to support consistency and ...
This role partners with Clinical Site Management Leadership to support monitoring excellence ... * Assist with review of monitoring trends and quality metrics to support consistency and ...
This role partners with Clinical Site Management Leadership to support monitoring excellence ... * Assist with review of monitoring trends and quality metrics to support consistency and ...
Evaluate monitoring effectiveness and identify opportunities for process improvements and ... * Assist in the development and maintenance of clinical procedures, work instructions, and ...
Evaluate monitoring effectiveness and identify opportunities for process improvements and ... * Assist in the development and maintenance of clinical procedures, work instructions, and ...
Serve as a liaison/resource for investigational sites. * Assist with RFPs and bid templates to ... Review/refine clinical operational plans including monitoring plan and other study plans.
Serve as a liaison/resource for investigational sites. * Assist with RFPs and bid templates to ... Review/refine clinical operational plans including monitoring plan and other study plans.
Clinical Research Associate (Pool)
CA · Remote
$90K - $130K/yr
Minimum of 2 years of experience in a Clinical Trial Assistant or other supporting project role with high attention to detail (3+ years of clinical monitoring experience preferred). * Prior ...
Clinical Research Associate (Pool)
CA · Remote
$90K - $130K/yr
Minimum of 2 years of experience in a Clinical Trial Assistant or other supporting project role with high attention to detail (3+ years of clinical monitoring experience preferred). * Prior ...
Clinical Operations Lead (Oncology)
$135K - $160K/yr
Develop a monitoring plan as well as monitoring tools. * Oversee the preparation, conduct and ... * Assist functional clinical operations delivery team. * Assist with the preparation and ...
Clinical Operations Lead (Oncology)
$135K - $160K/yr
Develop a monitoring plan as well as monitoring tools. * Oversee the preparation, conduct and ... * Assist functional clinical operations delivery team. * Assist with the preparation and ...
... Monitoring management. * Assist in the development and implementation of subject enrollment and recruitment strategies for site. * Manage and maintain visit information such as site/subject visit ...
... Monitoring management. * Assist in the development and implementation of subject enrollment and recruitment strategies for site. * Manage and maintain visit information such as site/subject visit ...
... Monitoring management. * Assist in the development and implementation of subject enrollment and recruitment strategies for site. * Manage and maintain visit information such as site/subject visit ...
... Monitoring management. * Assist in the development and implementation of subject enrollment and recruitment strategies for site. * Manage and maintain visit information such as site/subject visit ...
They may also support development of study-specific procedures (e.g., Monitoring Plans) and assist ... WEP Clinical partners with biopharmaceutical Sponsors to help them bring treatments closer to the ...
They may also support development of study-specific procedures (e.g., Monitoring Plans) and assist ... WEP Clinical partners with biopharmaceutical Sponsors to help them bring treatments closer to the ...
They may also support development of study-specific procedures (e.g., Monitoring Plans) and assist ... WEP Clinical partners with biopharmaceutical Sponsors to help them bring treatments closer to the ...
They may also support development of study-specific procedures (e.g., Monitoring Plans) and assist ... WEP Clinical partners with biopharmaceutical Sponsors to help them bring treatments closer to the ...
Develop a monitoring plan as well as monitoring tools. * Oversee the preparation, conduct and ... * Assist functional clinical operations delivery team. * Assist with the preparation and ...
Develop a monitoring plan as well as monitoring tools. * Oversee the preparation, conduct and ... * Assist functional clinical operations delivery team. * Assist with the preparation and ...
Clinical Research Associate
Fort Detrick, MD · On-site
$100K - $110K/yr
Generate clinical monitoring reports and follow-up letters. * Support site training and communication activities. * Track and assist with CAPA implementation. * Support audit and inspection readiness.
Quick apply
Clinical Research Associate
Fort Detrick, MD · On-site
$100K - $110K/yr
Generate clinical monitoring reports and follow-up letters. * Support site training and communication activities. * Track and assist with CAPA implementation. * Support audit and inspection readiness.
Clinical Research Associate
Fort Detrick, MD · On-site
$95K - $105K/yr
Generate clinical monitoring reports and follow-up letters. * Support site training and communication activities. * Track and assist with CAPA implementation. * Support audit and inspection readiness.
Clinical Research Associate
Fort Detrick, MD · On-site
$95K - $105K/yr
Generate clinical monitoring reports and follow-up letters. * Support site training and communication activities. * Track and assist with CAPA implementation. * Support audit and inspection readiness.
Clinical Research Associate
Fort Detrick, MD · On-site
$100K - $110K/yr
Generate clinical monitoring reports and follow-up letters. * Support site training and communication activities. * Track and assist with CAPA implementation. * Support audit and inspection readiness.
Clinical Research Associate
Fort Detrick, MD · On-site
$100K - $110K/yr
Generate clinical monitoring reports and follow-up letters. * Support site training and communication activities. * Track and assist with CAPA implementation. * Support audit and inspection readiness.
... * Assist with training new employees through co-monitoring * Coordinate designated clinical projects as a Local Project Coordinator, with supervision if applicable * Act as a local client contact as ...
... * Assist with training new employees through co-monitoring * Coordinate designated clinical projects as a Local Project Coordinator, with supervision if applicable * Act as a local client contact as ...
Clinical Monitoring Assistant information
See salary details
$11.54 - $13.11
1% of jobs
$13.11 - $14.69
5% of jobs
$14.69 - $16.26
15% of jobs
$16.57 is the 25th percentile. Wages below this are outliers.
$16.26 - $17.83
20% of jobs
The median wage is $18.86 / hr.
$17.83 - $19.41
14% of jobs
$19.41 - $20.98
13% of jobs
$20.98 - $22.55
7% of jobs
$22.60 is the 75th percentile. Wages above this are outliers.
$22.55 - $24.13
8% of jobs
$24.13 - $25.70
9% of jobs
$25.70 - $27.27
4% of jobs
$27.27 - $28.85
3% of jobs
$11
$20
$28
How much do clinical monitoring assistant jobs pay per hour?
As of Sep 12, 2026, the average hourly pay for clinical monitoring assistant in the United States is $20.23, according to ZipRecruiter salary data. Most workers in this role earn between $16.59 and $23.32 per hour, depending on experience, location, and employer.
What are the most commonly searched types of Clinical Monitoring jobs?
The most popular types of Clinical Monitoring jobs are:
What are popular job titles related to Clinical Monitoring Assistant jobs?
For Clinical Monitoring Assistant jobs, the most frequently searched job titles are:
Job description
The Clinical Monitor is primarily responsible for monitoring and validating clinical trial data, ensuring data quality, integrity, and compliance with regulatory requirements. This individual will work closely with the data management team and other stakeholders to facilitate accurate data collection and processing.
QUALIFICATIONS:- Bachelor’s degree in a life science, data science, or related field. However, a combination of experience and/or education will be taken into consideration.
- Minimum of 2 years of experience in clinical monitoring or data management within a Contract Research Organization (CRO), biotech, or pharmaceutical company.
- Understanding of GCP, FDA, and other regulatory requirements related to clinical monitoring.
- Excellent attention to detail and problem-solving skills.
- Good communication and interpersonal skills.
- Proficiency in clinical monitoring software and other relevant tools.
- Monitor and validate clinical trial data for accuracy, consistency, and completeness.
- Ensure compliance with data management and monitoring procedures, standards, and regulatory guidelines.
- Collaborate with data management and clinical trial teams to facilitate accurate and timely data collection and processing.
- Identify and resolve data discrepancies or issues in a timely manner.
- Participate in data audits and support the preparation of the clinical trial data for audits and inspections.
- Maintain up-to-date knowledge of regulatory requirements related to clinical monitoring.
- Assist in the development of clinical monitoring processes, standards, and training materials.
- Performs other duties as assigned.
This is a fully remote position and may be performed anywhere within the United States of America. Occasional domestic and international travel may be required for company meetings, site visits, audits, etc.
This Company participates in E-Verify and will provide the federal government with your Form I-9 information to confirm that you are authorized to work in the U.S.