Research Finance Analyst
Lexington, KY · On-site
The Research Financial Analyst oversees all financial functions within the Clinical Trial ... monitoring payment requests for participant reimbursements, internal departments, and external ...
Research Finance Analyst
Lexington, KY · On-site
The Research Financial Analyst oversees all financial functions within the Clinical Trial ... monitoring payment requests for participant reimbursements, internal departments, and external ...
$313 - $380/hr
Medical Monitoring*** Serves as an independent Medical Monitor for clinical trials by ... g., trial design, development strategy, regulatory strategy) based on merging data and multi ...
$313 - $380/hr
Medical Monitoring*** Serves as an independent Medical Monitor for clinical trials by ... g., trial design, development strategy, regulatory strategy) based on merging data and multi ...
$181 - $271/hr
You will own clinical trial diagnostic strategy, drive companion diagnostic co-development, and ... Ability to work in an office-based environment and perform essential functions with or without ...
New
$181 - $271/hr
You will own clinical trial diagnostic strategy, drive companion diagnostic co-development, and ... Ability to work in an office-based environment and perform essential functions with or without ...
New
$140 - $155/hr
... clinical trial programs by analyzing study timelines, enrollment assumptions, and projected spend. * Build and maintain financial models to evaluate financial performance, identify trends, monitor ...
$140 - $155/hr
... clinical trial programs by analyzing study timelines, enrollment assumptions, and projected spend. * Build and maintain financial models to evaluate financial performance, identify trends, monitor ...
$152 - $272/hr
Develop Trust Risk Program strategy and associated roadmaps, capability monitoring, and operation ... Facilitate fact-based, data-driven decision-making with the appropriate domain expertise and ...
$152 - $272/hr
Develop Trust Risk Program strategy and associated roadmaps, capability monitoring, and operation ... Facilitate fact-based, data-driven decision-making with the appropriate domain expertise and ...
Please note that this position is office based to be filled at our Covington, KY or Raleigh, NC ... Monitor and maintain tracking tools, clinical systems and shared document repositories utilized for ...
Please note that this position is office based to be filled at our Covington, KY or Raleigh, NC ... Monitor and maintain tracking tools, clinical systems and shared document repositories utilized for ...
Medical Director, Neuro-Oncology
Boston, KY · On-site
$250K - $316K/yr
S. is a Boston-based, commercial-stage biopharmaceutical company launched by Servier Group in 2018 ... Proven track record practicing sound medical judgment as it relates to clinical acumen and risk ...
Medical Director, Neuro-Oncology
Boston, KY · On-site
$250K - $316K/yr
S. is a Boston-based, commercial-stage biopharmaceutical company launched by Servier Group in 2018 ... Proven track record practicing sound medical judgment as it relates to clinical acumen and risk ...
$181 - $271/hr
You will own clinical trial diagnostic strategy, drive companion diagnostic co-development, and ... Experience managing external vendors/alliances and complex budgets; disciplined in risk management ...
New
$181 - $271/hr
You will own clinical trial diagnostic strategy, drive companion diagnostic co-development, and ... Experience managing external vendors/alliances and complex budgets; disciplined in risk management ...
New
$130 - $170/hr
Apply a risk-based approach to security control selection and specification, considering ... Experience with continuous monitoring strategies and tools to ensure ongoing system authorization ...
$130 - $170/hr
Apply a risk-based approach to security control selection and specification, considering ... Experience with continuous monitoring strategies and tools to ensure ongoing system authorization ...
$137 - $182/hr
... and risk-based audit plan for GxP computerized systems supporting clinical, manufacturing ... monitoring, continuous improvement, and alignment with enterprise risk management priorities.
$137 - $182/hr
... and risk-based audit plan for GxP computerized systems supporting clinical, manufacturing ... monitoring, continuous improvement, and alignment with enterprise risk management priorities.
Director, Therapeutic Strategy Lead - Level Dependent on Experience
Covington, KY · On-site +1
$18.50 - $25.25/hr
... trial oversight and execution activities * Collaborate with all CTI business units for effective ... Clinical Trials [DCT], remote-based monitoring [RBM], etc.) for protocol development and ...
Director, Therapeutic Strategy Lead - Level Dependent on Experience
Covington, KY · On-site +1
$18.50 - $25.25/hr
... trial oversight and execution activities * Collaborate with all CTI business units for effective ... Clinical Trials [DCT], remote-based monitoring [RBM], etc.) for protocol development and ...
Director, Therapeutic Strategy Lead - Level Dependent on Experience
Covington, KY · On-site +1
$18.50 - $25.25/hr
... trial oversight and execution activities * Collaborate with all CTI business units for effective ... Clinical Trials [DCT], remote-based monitoring [RBM], etc.) for protocol development and ...
Director, Therapeutic Strategy Lead - Level Dependent on Experience
Covington, KY · On-site +1
$18.50 - $25.25/hr
... trial oversight and execution activities * Collaborate with all CTI business units for effective ... Clinical Trials [DCT], remote-based monitoring [RBM], etc.) for protocol development and ...
Director, Translational Research and Biomarkers
Princeton, KY · On-site
$186 - $279/hr
Initiates experimental design discussions based on existing gaps in clinical trial data and aids in development of biomarker and genomic research plans in collaboration with Bioanalysis, Genomics ...
Director, Translational Research and Biomarkers
Princeton, KY · On-site
$186 - $279/hr
Initiates experimental design discussions based on existing gaps in clinical trial data and aids in development of biomarker and genomic research plans in collaboration with Bioanalysis, Genomics ...
$150 - $210/hr
Reporting to the SVP and Head of Clinical Trial Services, this role will assess current research ... Monitor progress against the platform roadmap and refine the strategy based on performance data and ...
$150 - $210/hr
Reporting to the SVP and Head of Clinical Trial Services, this role will assess current research ... Monitor progress against the platform roadmap and refine the strategy based on performance data and ...
$296 - $493/hr
Integrates regulatory and statistical input into clinical trial design * Drives and implements ... Drives risk management, issue identification and resolution and contingency planning * Create a ...
New
$296 - $493/hr
Integrates regulatory and statistical input into clinical trial design * Drives and implements ... Drives risk management, issue identification and resolution and contingency planning * Create a ...
New
$70 - $90/hr
Our founders pioneered community-based cancer care because they believed in making the best ... Present trial concepts and details to oncology patients while conducting the informed consent ...
$70 - $90/hr
Our founders pioneered community-based cancer care because they believed in making the best ... Present trial concepts and details to oncology patients while conducting the informed consent ...
$120 - $165/hr
... de-risk and accelerate our partners' most high-profile drug and device programs.**Essential ... Experience in clinical trial design, sample size calculations, and statistical analysis.
$120 - $165/hr
... de-risk and accelerate our partners' most high-profile drug and device programs.**Essential ... Experience in clinical trial design, sample size calculations, and statistical analysis.
Dietitian (Clinical)
Louisville, KY · On-site +1
$83K - $108K/yr
Upon completion of your trial period, your employment will be terminated unless you receive ... monitoring, and evaluation). * Skill in interpreting research to apply evidence-based nutrition ...
Dietitian (Clinical)
Louisville, KY · On-site +1
$83K - $108K/yr
Upon completion of your trial period, your employment will be terminated unless you receive ... monitoring, and evaluation). * Skill in interpreting research to apply evidence-based nutrition ...
$180 - $240/hr
Aerogen Pharma is a US based clinical-stage specialty pharmaceutical company with a mission to ... Contribute to safety oversight activities, including review of adverse events, risk management ...
$180 - $240/hr
Aerogen Pharma is a US based clinical-stage specialty pharmaceutical company with a mission to ... Contribute to safety oversight activities, including review of adverse events, risk management ...
Dietitian (Clinical)
Louisville, KY · On-site
Upon completion of your trial period, your employment will be terminated unless you receive ... monitoring, and evaluation). Skill in interpreting research to apply evidence-based nutrition ...
Dietitian (Clinical)
Louisville, KY · On-site
Upon completion of your trial period, your employment will be terminated unless you receive ... monitoring, and evaluation). Skill in interpreting research to apply evidence-based nutrition ...
Clinical Trial Risk Based Monitoring information
What is clinical trial risk based monitoring?
Clinical Trial Risk Based Monitoring (RBM) is a strategy used in clinical research to prioritize and focus monitoring activities on the most critical risks to patient safety and data integrity. Instead of monitoring every data point equally, RBM uses data analytics and risk assessment tools to identify which sites, processes, or data require more attention. This approach increases efficiency, reduces costs, and helps ensure that potential issues are detected and addressed promptly. RBM is supported by regulatory agencies and is increasingly adopted in both large and small clinical trials.
How does a clinical trial risk based monitoring professional typically collaborate with cross-functional teams during a study?
In a Clinical Trial Risk Based Monitoring role, you will regularly work with clinical research associates, data managers, statisticians, and regulatory teams to identify and address potential risks throughout a study. Collaboration often involves participating in meetings to review data trends, sharing insights about site performance, and helping to develop mitigation strategies. Effective communication is crucial, as you will be responsible for ensuring that all stakeholders are informed of key risks and recommended actions. This collaborative environment helps drive patient safety, data integrity, and overall trial success.
What are the key skills and qualifications needed to thrive in clinical trial risk based monitoring, and why are they important?
To thrive in Clinical Trial Risk Based Monitoring, you need expertise in clinical research, regulatory compliance, and data analysis, usually supported by a degree in life sciences or related fields. Familiarity with risk assessment tools, EDC (Electronic Data Capture) systems, and GCP (Good Clinical Practice) certification is typically required. Strong attention to detail, critical thinking, and effective communication help professionals proactively identify and address potential risks in trials. These skills are crucial for maintaining data integrity, ensuring patient safety, and optimizing the efficiency and quality of clinical studies.
What is the difference between Clinical Trial Risk Based Monitoring vs Clinical Trial Data Manager?
| Aspect | Clinical Trial Risk Based Monitoring | Clinical Trial Data Manager |
|---|---|---|
| Primary Focus | Monitoring trial sites for risks and compliance | Managing and ensuring accuracy of trial data |
| Required Skills | Monitoring protocols, regulatory knowledge, site management | Data management, database systems, quality control |
| Work Environment | Clinical sites, monitoring visits, remote oversight | Data centers, clinical trial databases, office setting |
| Certifications | GCP, monitoring certifications | CDMP, data management certifications |
While both roles are integral to clinical trials, Risk Based Monitoring focuses on overseeing site performance and compliance to mitigate risks, whereas Data Managers concentrate on managing and validating trial data for accuracy and integrity.
What are popular job titles related to Clinical Trial Risk Based Monitoring jobs in Kentucky?
For Clinical Trial Risk Based Monitoring jobs in Kentucky, the most frequently searched job titles are:
What job categories do people searching Clinical Trial Risk Based Monitoring jobs in Kentucky look for?
The top searched job categories for Clinical Trial Risk Based Monitoring jobs in Kentucky are:
What cities in Kentucky are hiring for Clinical Trial Risk Based Monitoring jobs?
Cities in Kentucky with the most Clinical Trial Risk Based Monitoring job openings:
Baptist Health South Florida rating
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Job description
Summary
Job Description:
Baptist Health is looking for a Research Finance Analyst to join our team in Lexington, KY!
The Research Financial Analyst is responsible for financial management within the Office of Research Administration, supporting the financial oversight of clinical trials across the health system. This role works closely with the Research Finance management, Finance team, and the clinical research team to manage the complete financial life cycle of clinical trials-from study startup through closeout. The Research Financial Analyst oversees all financial functions within the Clinical Trial Management System (CTMS), including the development, maintenance, and reconciliation of study budgets, as well as the accurate recording, allocation, and tracking of study-related financial transactions.
The analyst researches and analyzes accounting data to provide timely and accurate financial information to leadership. Key responsibilities include building study budgets in the CTMS; payment coding; processing deposits and allocating funds within the CTMS; maintaining the accounts receivable tracker; generating invoices for subject visits, administrative fees, and all other billable items outlined in the Clinical Trial Agreement (CTA); and submitting invoices for industry-sponsored studies and all applicable federal studies through CTSU OPEN. The role also manages accounts payable by maintaining the payable tracker, submitting and monitoring payment requests for participant reimbursements, internal departments, and external vendors.
The Research Financial Analyst ensures that study closeout is completed in accordance with departmental procedures and prepares financial reports as needed. This position plays a central role in maintaining financial accuracy, regulatory compliance, and the overall fiscal integrity of the research program.
Qualifications:
If you would like to be part of a growing family focused on supporting clinical excellence, teamwork and innovation, we urge you to apply now!
Baptist Health is an Equal Employment Opportunity employer.
Job Description:
Baptist Health is looking for a Research Finance Analyst to join our team in Lexington, KY!
The Research Financial Analyst is responsible for financial management within the Office of Research Administration, supporting the financial oversight of clinical trials across the health system. This role works closely with the Research Finance management, Finance team, and the clinical research team to manage the complete financial life cycle of clinical trials-from study startup through closeout. The Research Financial Analyst oversees all financial functions within the Clinical Trial Management System (CTMS), including the development, maintenance, and reconciliation of study budgets, as well as the accurate recording, allocation, and tracking of study-related financial transactions.
The analyst researches and analyzes accounting data to provide timely and accurate financial information to leadership. Key responsibilities include building study budgets in the CTMS; payment coding; processing deposits and allocating funds within the CTMS; maintaining the accounts receivable tracker; generating invoices for subject visits, administrative fees, and all other billable items outlined in the Clinical Trial Agreement (CTA); and submitting invoices for industry-sponsored studies and all applicable federal studies through CTSU OPEN. The role also manages accounts payable by maintaining the payable tracker, submitting and monitoring payment requests for participant reimbursements, internal departments, and external vendors.
The Research Financial Analyst ensures that study closeout is completed in accordance with departmental procedures and prepares financial reports as needed. This position plays a central role in maintaining financial accuracy, regulatory compliance, and the overall fiscal integrity of the research program.
Qualifications:
- Bachelor's degree in accounting, finance or health administration.
- 5 years job-related experience.
- Four or more additional years of experience in clinical research, medical billing/coding, healthcare compliance/auditing, or equivalent experience in accounting/finance in lieu of a bachelor's degree.
- Strong proficiency in Microsoft Excel (advanced formulas, pivot tables, modeling, Power Query).
- Experience working with clinical trials or healthcare financial data.
- Excellent analytical, problem-solving, and quantitative skills.
- Ability to interpret clinical procedures, tests, and care pathways for financial impact.
- Basic programming and reporting experience.
- Knowledge of clinical research billing compliance and healthcare reimbursement models.
- Five years of experience managing high-volume Accounts Payable and Accounts Receivable operations.
- Experience with Clinical Trial Management Systems (CTMS) preferred.
- Exposure to reporting tools or basic programming preferred.
- Experience in clinical research finance, healthcare finance, or related field
- Demonstrated experience working with clinical trial budgets, financial systems, and research billing processes
If you would like to be part of a growing family focused on supporting clinical excellence, teamwork and innovation, we urge you to apply now!
Baptist Health is an Equal Employment Opportunity employer.
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About Baptist Health South Florida
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Baptist Health South Florida is the largest healthcare organization in the region, with 12 hospitals, more than 27,000 employees, 4,000 physicians and 100 outpatient centers, urgent care facilities and physician practices spanning across Miami-Dade, Monroe, Broward and Palm Beach counties. Baptist Health has internationally renowned centers of excellence in cancer, cardiovascular care, orthopedics and sports medicine, and neurosciences. A not-for-profit organization supported by philanthropy and committed to its faith-based charitable mission of medical excellence, Baptist Health has been recognized by Fortune as one of the 100 Best Companies to Work For in America and by Ethisphere as one of the World's Most Ethical Companies.
Industry
Health care and social assistance
Company size
10,000+ Employees
Headquarters location
Miami, FL, US