... Clinical Trial Policy for all clinical trials. The billing analysis must be compliant with the Medicare billing rules. This position also serves as liaison with the investigators, research teams ...
... Clinical Trial Policy for all clinical trials. The billing analysis must be compliant with the Medicare billing rules. This position also serves as liaison with the investigators, research teams ...
Clinical Trial Analyst, Full Time, Day
Linthicum, MD · On-site
$333K/yr
... Clinical Trial Policy for all clinical trials. The billing analysis must be compliant with the Medicare billing rules. This position also serves as liaison with the investigators, research teams ...
Clinical Trial Analyst, Full Time, Day
Linthicum, MD · On-site
$333K/yr
... Clinical Trial Policy for all clinical trials. The billing analysis must be compliant with the Medicare billing rules. This position also serves as liaison with the investigators, research teams ...
The Clinical Trial Analyst is responsible for developing Coverage Analyses (CAs), negotiating clinical trial budgets, and supporting the financial feasibility of industry-sponsored, co-operative ...
The Clinical Trial Analyst is responsible for developing Coverage Analyses (CAs), negotiating clinical trial budgets, and supporting the financial feasibility of industry-sponsored, co-operative ...
The Clinical Trial Analyst is responsible for developing Coverage Analyses (CAs), negotiating clinical trial budgets, and supporting the financial feasibility of industry-sponsored, co-operative ...
The Clinical Trial Analyst is responsible for developing Coverage Analyses (CAs), negotiating clinical trial budgets, and supporting the financial feasibility of industry-sponsored, co-operative ...
... Analysts' 2012 annual report. Artech provides technical expertise to fill gaps in clients ... Accountable for all internal clinical meetings related to the clinical trial(s). 4. Lead and matrix ...
... Analysts' 2012 annual report. Artech provides technical expertise to fill gaps in clients ... Accountable for all internal clinical meetings related to the clinical trial(s). 4. Lead and matrix ...
Clinical Trial Manager
San Diego, CA · Remote
$110K - $140K/yr
Contributes to relevant trial documentation including clinical protocols, statistical analysis plan, clinical trial reports as well as operational plans (CMP, DMP). * Reviews and refines clinical ...
Clinical Trial Manager
San Diego, CA · Remote
$110K - $140K/yr
Contributes to relevant trial documentation including clinical protocols, statistical analysis plan, clinical trial reports as well as operational plans (CMP, DMP). * Reviews and refines clinical ...
Clinical Trial Manager
San Diego, CA · On-site
$110K - $140K/yr
Contributes to relevant trial documentation including clinical protocols, statistical analysis plan, clinical trial reports as well as operational plans (CMP, DMP). * Reviews and refines clinical ...
Quick apply
Clinical Trial Manager
San Diego, CA · On-site
$110K - $140K/yr
Contributes to relevant trial documentation including clinical protocols, statistical analysis plan, clinical trial reports as well as operational plans (CMP, DMP). * Reviews and refines clinical ...
Clinical Trial Manager
San Diego, CA · On-site
$110K - $140K/yr
Contributes to relevant trial documentation including clinical protocols, statistical analysis plan, clinical trial reports as well as operational plans (CMP, DMP). * Reviews and refines clinical ...
Clinical Trial Manager
San Diego, CA · On-site
$110K - $140K/yr
Contributes to relevant trial documentation including clinical protocols, statistical analysis plan, clinical trial reports as well as operational plans (CMP, DMP). * Reviews and refines clinical ...
Clinical Trial Manager/Sr Clinical Trial Manager
$145K - $190K/yr
The Clinical Trial Manager or Senior Clinical Trial Manager assists in the planning, implementation ... Monitor and track biological samples for applicable analyses. * Provide progress updates to ...
Quick apply
Clinical Trial Manager/Sr Clinical Trial Manager
$145K - $190K/yr
The Clinical Trial Manager or Senior Clinical Trial Manager assists in the planning, implementation ... Monitor and track biological samples for applicable analyses. * Provide progress updates to ...
Clinical Trial Manager/Sr Clinical Trial Manager
$145K - $190K/yr
Monitor and track biological samples for applicable analyses. * Provide progress updates to ... For Clinical Trial Manager, at least 5 years of relevant experience in oncology clinical operations ...
Clinical Trial Manager/Sr Clinical Trial Manager
$145K - $190K/yr
Monitor and track biological samples for applicable analyses. * Provide progress updates to ... For Clinical Trial Manager, at least 5 years of relevant experience in oncology clinical operations ...
... analyses, the AP3 Kinase Substrate Relationship Predictor and the AP3 Interactome. These ... The Clinical Trial Manager position focuses on strategic planning, implementation, and management ...
... analyses, the AP3 Kinase Substrate Relationship Predictor and the AP3 Interactome. These ... The Clinical Trial Manager position focuses on strategic planning, implementation, and management ...
Clinical Trial Manager/Sr Clinical Trial Manager
San Diego, CA · On-site +1
$145K - $190K/yr
The Clinical Trial Manager or Senior Clinical Trial Manager assists in the planning, implementation ... Monitor and track biological samples for applicable analyses. * Provide progress updates to ...
Clinical Trial Manager/Sr Clinical Trial Manager
San Diego, CA · On-site +1
$145K - $190K/yr
The Clinical Trial Manager or Senior Clinical Trial Manager assists in the planning, implementation ... Monitor and track biological samples for applicable analyses. * Provide progress updates to ...
The Clinical Trial Manager or Senior Clinical Trial Manager assists in the planning, implementation ... Monitor and track biological samples for applicable analyses. * Provide progress updates to ...
Quick apply
The Clinical Trial Manager or Senior Clinical Trial Manager assists in the planning, implementation ... Monitor and track biological samples for applicable analyses. * Provide progress updates to ...
Clinical Trial Manager (CTM) Location: Hampton, NJ Duration: 6 Months (Possible extension) SUMMARY ... Solid project management, analytical and problem solving skills. Travel as needed to resolve field ...
Clinical Trial Manager (CTM) Location: Hampton, NJ Duration: 6 Months (Possible extension) SUMMARY ... Solid project management, analytical and problem solving skills. Travel as needed to resolve field ...
Clinical Trial Manager
Watertown, MA · On-site
$130K - $150K/yr
... analyses, the AP3 Kinase Substrate Relationship Predictor and the AP3 Interactome. These ... Position Overview: The Clinical Trial Manager will be a key member of Acrivon Therapeutics ...
Clinical Trial Manager
Watertown, MA · On-site
$130K - $150K/yr
... analyses, the AP3 Kinase Substrate Relationship Predictor and the AP3 Interactome. These ... Position Overview: The Clinical Trial Manager will be a key member of Acrivon Therapeutics ...
POSITION SUMMARY This Clinical Trial Manager role is responsible for leading the end-to-end ... Knowledge of adverse event investigation, analysis and reporting procedures and standards
New
POSITION SUMMARY This Clinical Trial Manager role is responsible for leading the end-to-end ... Knowledge of adverse event investigation, analysis and reporting procedures and standards
New
Clinical Trial Manager
Watertown, MA · On-site
... analyses, the AP3 Kinase Substrate Relationship Predictor and the AP3 Interactome. These ... The Clinical Trial Manager position focuses on strategic planning, implementation, and management ...
Quick apply
Clinical Trial Manager
Watertown, MA · On-site
... analyses, the AP3 Kinase Substrate Relationship Predictor and the AP3 Interactome. These ... The Clinical Trial Manager position focuses on strategic planning, implementation, and management ...
Clinical Trial Manager
San Mateo, CA · On-site
$90 - $135/hr
Job Type Contract Description The Clinical Trial Manager manages and leads the day-to-day clinical ... analysis process at the study level and may perform reconciliation and/or tracking of sample ...
Clinical Trial Manager
San Mateo, CA · On-site
$90 - $135/hr
Job Type Contract Description The Clinical Trial Manager manages and leads the day-to-day clinical ... analysis process at the study level and may perform reconciliation and/or tracking of sample ...
Clinical Trial Manager
Watertown, MA · On-site
... analyses, the AP3 Kinase Substrate Relationship Predictor and the AP3 Interactome. These ... Position Overview: The Clinical Trial Manager will be a key member of Acrivon Therapeutics ...
Quick apply
Clinical Trial Manager
Watertown, MA · On-site
... analyses, the AP3 Kinase Substrate Relationship Predictor and the AP3 Interactome. These ... Position Overview: The Clinical Trial Manager will be a key member of Acrivon Therapeutics ...
Clinical Trial Manager
$90 - $100/hr
Description The Clinical Trial Manager manages and leads the day-to-day clinical trial activities ... Knowledge of sample collect and analysis process at the study level and may perform reconciliation ...
Clinical Trial Manager
$90 - $100/hr
Description The Clinical Trial Manager manages and leads the day-to-day clinical trial activities ... Knowledge of sample collect and analysis process at the study level and may perform reconciliation ...
Clinical Trial Analyst information
See salary details
$18.03 - $22.03
1% of jobs
$22.03 - $26.03
5% of jobs
$26.03 - $30.03
16% of jobs
$30.86 is the 25th percentile. Wages below this are outliers.
$30.03 - $34.03
13% of jobs
$34.03 - $38.02
13% of jobs
The median wage is $38.49 / hr.
$38.02 - $42.02
18% of jobs
$44.64 is the 75th percentile. Wages above this are outliers.
$42.02 - $46.02
14% of jobs
$46.02 - $50.02
9% of jobs
$50.02 - $54.02
5% of jobs
$54.02 - $58.02
3% of jobs
$58.02 - $62.02
3% of jobs
$18
$39
$62
How much do clinical trial analyst jobs pay per hour?
What does a Clinical Trial Analyst do?
What is the difference between Clinical Trial Analyst vs Clinical Research Coordinator?
| Aspect | Clinical Trial Analyst | Clinical Research Coordinator |
|---|---|---|
| Required Credentials | Bachelor's degree in life sciences, biostatistics, or related field; some roles may require certification in clinical research | Bachelor's degree in health sciences, nursing, or related field; often requires certification in clinical research coordination |
| Work Environment | Data analysis, report preparation, and monitoring clinical trial data | Managing trial logistics, patient recruitment, and site coordination |
| Employer & Industry Usage | Pharmaceutical companies, CROs, biotech firms | Hospitals, research institutions, clinical trial sites |
While both roles support clinical trials, Clinical Trial Analysts focus on data analysis and reporting, whereas Clinical Research Coordinators handle trial logistics and patient management. Both positions require similar educational backgrounds and certifications, but their daily tasks and work environments differ significantly.
What are the key skills and qualifications needed to thrive as a Clinical Trial Analyst, and why are they important?
What are some common challenges faced by Clinical Trial Analysts when managing multiple studies simultaneously?

Full-time
Posted 17 days ago
Job description
I.              General Summary
Under limited supervision, and with the latitude for initiative and independent judgment, performs, coordinates, and manages the creation and outsourcing of billing analysis in accordance with the Center for Medicaid and Medicare Services (CMS) regulations and the Clinical Trial Policy for all clinical trials. The billing analysis must be compliant with the Medicare billing rules.
This position also serves as liaison with the investigators, research teams, healthcare providers, budgeting and contracting offices at UMMS and UMB, and in coordination with departmental clinical trial management processes. This position works with various systems including Epic and HPM Explorer for the purpose of segregating charges to ensure compliant billing for research services as well as providing pricing for budgeting purposes.
II.            Principal Responsibilities and Tasks
The following statements are intended to describe the general nature and level of work being performed by people assigned to this classification. These are not to be construed as an exhaustive list of all job duties performed by personnel so classified.
1.     Creates coverage analysis grids and analyzes the performance of the actual coverage analysis.
2.     Performs basic and complex billing and budget analysis in accordance with CMS regulations for all clinical trials performed at UMMS affiliates and FPI practice offices and clinics.
3.     Applies CMS regulations, FDA guidance, and ethical policies when performing coverage analysis.
4.     Develops the coverage analysis including reviewing each potentially billable item within the clinical trial and citing specific resources for justification of the appropriate designations.
5.     Applies the appropriate CDM and/or CPT codes for potentially billable items in the coverage analysis in order to assist in the management of claims review, as well as identifying items that are to be billed to the sponsor via the budgeting and contract teams at the Office of Research and Development (ORD) at University of Baltimore (UMB).
6.     Collaborates with research teams in performing the coverage analysis, as well as facilitating the clinical trial management process involving UMB, UMMS, and FPI.
7.     Researches and applies regulations and law related to Medicare regulations, OIG regulations, FDA guidance, and related compliance documents using various resources including computer search modalities.
8.     Synchronizes the final coverage analysis with appropriate final study documents.
9.     Triages coverage analysis requests to our coverage analysis vendor when applicable. Acts as the intermediary between the vendor and the study teams during coverage analysis creation, tracks progress, and reports results.
10.  Researches and applies policies, guidance and guidelines from various sources including federal, state, UMMS and the University of Maryland Baltimore (UMB).
11.  Responsible for the dissemination of relevant documents and information to various parties.
12.  Serves as liaison and contact with the clinical research teams and healthcare providers.
13.  Segregates charges in Epic by distinguishing research charges billed to the study versus those research charges that can be billed to insurance.
14.  Reviews and resolves invoice discrepancies with the Central Billing Office and the study teams,
15.  Creates Epic RSH Records and Fee Schedules for each research study.
16.  Performs monthly coverage analysis and charge segregation audits to ensure ongoing compliance.
17.  Other duties as assigned.
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Work Experience
Education and Experience
1.     Bachelor's degree in Healthcare Administration, Medical Coding, Auditing, Finance, Accounting, Nursing, or a related field required.
2.     Four (4) years of clinical research experience required. Additional experience may be substituted for the educational requirement on a year-for-year basis for up to four (4) years.
3.     Certification in Healthcare Research Compliance or Epic preferred.
IV.        Knowledge, Skills, and Abilities
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1.     Knowledge of principles and practices pertaining to developing and administering a clinical trial in compliance with sponsor, federal, state, UMMS and University of Maryland Baltimore regulations.
2.     Demonstrated skill tracking clinical and corporate contracts using electronic administration software such as Grant.gov, CICERO, OnCore, Epic, etc.
3.     Skill in cost/financial accounting and clinical trial management software.
4.     Expert knowledge of spreadsheets (i.e. Microsoft Excel), databases (i.e., DBASE, Microsoft Access), word processing programs (i.e., Microsoft Word), and graphic/specialty and other finance-related software programs.
5.     Highly effective verbal and written communication skills are necessary in dealing with a variety of healthcare and finance professionals including senior management staff.
6.     Ability to assess and evaluate complex financial data via use of computer analysis.
7.     Proficient organization and problem-solving skills are required to develop/implement efficient work processes. Ability to work effectively in a stressful work environment.  Ability to work independently in a matrix work environment.
8.     Must maintain knowledge of developments/changes in the field of Research Billing Compliance as well as maintain currency on applicable regulations and procedures affecting hospital and physician finance and regulatory practices.
9.     Maintains familiarity with current regulations involved with compliant billing practices.
10.  Skill in planning, analyzing and coordinating activities and establishing priorities.
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Employment Type: FULL_TIME