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North Bethesda, MD · On-site
$115K - $135K/yr
Minimum 10 years of Good Clinical Practice (GCP) clinical trial monitoring experience. * Minimum 5 years of monitoring or auditing federally funded clinical research studies (VA, NIH, DoD, CDC, or ...
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Be Seen First
North Bethesda, MD · On-site
$115K - $135K/yr
Minimum 10 years of Good Clinical Practice (GCP) clinical trial monitoring experience. * Minimum 5 years of monitoring or auditing federally funded clinical research studies (VA, NIH, DoD, CDC, or ...
Director, Clinical Trial Finance Our client, a publicly traded life sciences company, is seeking a ... Support audit readiness efforts and collaborate with internal and external auditors as needed.
New
Director, Clinical Trial Finance Our client, a publicly traded life sciences company, is seeking a ... Support audit readiness efforts and collaborate with internal and external auditors as needed.
New
The Trial Supplies Operations Manager is responsible for the implementation of appropriate Clinical ... auditors. Interaction with local country representatives (IPM) and depots to coordinate over ...
The Trial Supplies Operations Manager is responsible for the implementation of appropriate Clinical ... auditors. Interaction with local country representatives (IPM) and depots to coordinate over ...
$130K - $216K/yr
Clinical Trial Operations Travel Required: None Clearance Required: Ability to Obtain Public Trust What You Will Do: We are currently searching for a Clinical Trials Program Monitor and Auditor to ...
$130K - $216K/yr
Clinical Trial Operations Travel Required: None Clearance Required: Ability to Obtain Public Trust What You Will Do: We are currently searching for a Clinical Trials Program Monitor and Auditor to ...
The Trial Supplies Operations Manager is responsible for the implementation of appropriate Clinical ... auditors. Interaction with local country representatives (IPM) and depots to coordinate over ...
The Trial Supplies Operations Manager is responsible for the implementation of appropriate Clinical ... auditors. Interaction with local country representatives (IPM) and depots to coordinate over ...
Bethesda, MD · On-site
$130K - $216K/yr
Clinical Trial Operations Travel Required: None Clearance Required: Ability to Obtain Public Trust What You Will Do: We are currently searching for a Clinical Trials Program Monitor and Auditor to ...
Bethesda, MD · On-site
$130K - $216K/yr
Clinical Trial Operations Travel Required: None Clearance Required: Ability to Obtain Public Trust What You Will Do: We are currently searching for a Clinical Trials Program Monitor and Auditor to ...
$62K - $69K/yr
CLINICAL TRIAL RESEARCH BILLING ANALYST *We do not consider incomplete or Quick Apply applications ... auditing, monitoring, and research billing and collections. BRANY was founded in 1998 and is owned ...
$62K - $69K/yr
CLINICAL TRIAL RESEARCH BILLING ANALYST *We do not consider incomplete or Quick Apply applications ... auditing, monitoring, and research billing and collections. BRANY was founded in 1998 and is owned ...
Melville, NY · On-site
$62K - $69K/yr
CLINICAL TRIAL RESEARCH BILLING ANALYST Applicants must apply at: About the Organization ... auditing, monitoring, and research billing and collections. BRANY was founded in 1998 and is owned ...
New
Melville, NY · On-site
$62K - $69K/yr
CLINICAL TRIAL RESEARCH BILLING ANALYST Applicants must apply at: About the Organization ... auditing, monitoring, and research billing and collections. BRANY was founded in 1998 and is owned ...
New
Brookline, MA · Hybrid
$61K - $67K/yr
Assists in the preparation and coordination of assigned study monitoring and auditing visits with ... Communicate and collaborate with clinical trial key stakeholders through the start-up process ...
Brookline, MA · Hybrid
$61K - $67K/yr
Assists in the preparation and coordination of assigned study monitoring and auditing visits with ... Communicate and collaborate with clinical trial key stakeholders through the start-up process ...
New Brunswick, NJ · On-site +1
$75K - $100K/yr
Help modernize clinical trial budgeting and billing processes using technology and best practices ... Bachelor's degree in Healthcare Administration, Medical Coding, Auditing, Finance, Accounting ...
New Brunswick, NJ · On-site +1
$75K - $100K/yr
Help modernize clinical trial budgeting and billing processes using technology and best practices ... Bachelor's degree in Healthcare Administration, Medical Coding, Auditing, Finance, Accounting ...
$75 - $100/hr
Help modernize clinical trial budgeting and billing processes using technology and best practices ... Bachelor's degree in Healthcare Administration, Medical Coding, Auditing, Finance, Accounting ...
$75 - $100/hr
Help modernize clinical trial budgeting and billing processes using technology and best practices ... Bachelor's degree in Healthcare Administration, Medical Coding, Auditing, Finance, Accounting ...
Help modernize clinical trial budgeting and billing processes using technology and best practices ... Bachelor's degree in Healthcare Administration, Medical Coding, Auditing, Finance, Accounting ...
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Help modernize clinical trial budgeting and billing processes using technology and best practices ... Bachelor's degree in Healthcare Administration, Medical Coding, Auditing, Finance, Accounting ...
Chicago, IL · On-site
$75 - $100/hr
Help modernize clinical trial budgeting and billing processes using technology and best practices ... Bachelor's degree in Healthcare Administration, Medical Coding, Auditing, Finance, Accounting ...
Chicago, IL · On-site
$75 - $100/hr
Help modernize clinical trial budgeting and billing processes using technology and best practices ... Bachelor's degree in Healthcare Administration, Medical Coding, Auditing, Finance, Accounting ...
Marrero, LA · On-site
$73K - $101K/yr
This position plays a key role in the accuracy and consistency of clinical trial data by preventing ... Auditors, and central rating organizations * Articulate rating concerns or issues to the CRO ...
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Marrero, LA · On-site
$73K - $101K/yr
This position plays a key role in the accuracy and consistency of clinical trial data by preventing ... Auditors, and central rating organizations * Articulate rating concerns or issues to the CRO ...
Be Seen First
... auditing. OVERALL RESPONSIBILITIES: The Clinical Trials Project Manager will: * Develop/implement ... Provide training to clients and internal staff on such areas as clinical trial management, good ...
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Be Seen First
... auditing. OVERALL RESPONSIBILITIES: The Clinical Trials Project Manager will: * Develop/implement ... Provide training to clients and internal staff on such areas as clinical trial management, good ...
$82K - $101K/yr
Position Summary The Senior GCP Auditor ensures GCP compliance with ImmunityBio entity standard ... Maintain and update the Clinical Trial Quality Management system to be current with industry ...
$82K - $101K/yr
Position Summary The Senior GCP Auditor ensures GCP compliance with ImmunityBio entity standard ... Maintain and update the Clinical Trial Quality Management system to be current with industry ...
Morgantown, WV · On-site
$25 - $33.25/hr
Performs a variety of duties involved in clinical trial coordination and implementation ... Observes scheduled and unscheduled meetings with external and internal monitors and auditors ...
Morgantown, WV · On-site
$25 - $33.25/hr
Performs a variety of duties involved in clinical trial coordination and implementation ... Observes scheduled and unscheduled meetings with external and internal monitors and auditors ...
$82K - $101K/yr
Position Summary The Senior GCP Auditor ensures GCP compliance with ImmunityBio entity standard ... Maintain and update the Clinical Trial Quality Management system to be current with industry ...
$82K - $101K/yr
Position Summary The Senior GCP Auditor ensures GCP compliance with ImmunityBio entity standard ... Maintain and update the Clinical Trial Quality Management system to be current with industry ...
$195K - $227K/yr
Experience with electronic Quality Management Systems and Trial Master File. * Auditor certification is preferred. * Up to 60% travel may be required. * Experience in managing or supporting clinical ...
$195K - $227K/yr
Experience with electronic Quality Management Systems and Trial Master File. * Auditor certification is preferred. * Up to 60% travel may be required. * Experience in managing or supporting clinical ...
Culver City, CA · On-site
$88K - $108K/yr
Position Summary The Senior GCP Auditor ensures GCP compliance with ImmunityBio entity standard ... Maintain and update the Clinical Trial Quality Management system to be current with industry ...
Culver City, CA · On-site
$88K - $108K/yr
Position Summary The Senior GCP Auditor ensures GCP compliance with ImmunityBio entity standard ... Maintain and update the Clinical Trial Quality Management system to be current with industry ...
$17.31 - $22.12
4% of jobs
$22.12 - $26.92
8% of jobs
$26.92 - $31.73
12% of jobs
$31.88 is the 25th percentile. Wages below this are outliers.
$31.73 - $36.54
26% of jobs
$36.54 - $41.35
18% of jobs
$43.02 is the 75th percentile. Wages above this are outliers.
$41.35 - $46.15
19% of jobs
$46.15 - $50.96
6% of jobs
$50.96 - $55.77
2% of jobs
$55.77 - $60.58
1% of jobs
$60.58 - $65.38
1% of jobs
$65.38 - $70.19
2% of jobs
$17
$39
$70
A Clinical Trial Auditor assesses clinical trials to ensure compliance with regulations, protocols, and ethical standards. They review documentation, procedures, and data integrity to ensure that trials meet Good Clinical Practice (GCP) guidelines and regulatory requirements. Auditors identify potential risks, recommend corrective actions, and help maintain the overall quality and credibility of clinical research. Their role is critical in ensuring the safety of trial participants and the validity of study results.
A Clinical Trial Auditor requires a strong background in clinical research, regulatory compliance (such as GCP and FDA guidelines), and a relevant scientific or healthcare degree. Familiarity with electronic trial master file (eTMF) systems, auditing methodologies, and certifications like ASQ Certified Quality Auditor or RQAP-GCP are highly valued. Excellent attention to detail, analytical thinking, and effective communication skills are important soft skills in this role. These competencies ensure thorough oversight, accurate documentation, and adherence to regulatory standards, which are vital for the integrity and success of clinical trials.
Clinical Trial Auditors often encounter challenges such as navigating complex regulatory requirements, identifying discrepancies in documentation, and ensuring consistent protocol adherence across multiple sites. Managing these issues requires strong organizational skills, constant communication with clinical teams, and staying up to date with evolving guidelines. Auditors frequently collaborate with study coordinators, principal investigators, and regulatory affairs professionals to address findings and recommend corrective actions. Successfully handling these challenges is essential for maintaining compliance and supporting the reliability of clinical trial results.
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