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Clinical Research Finance Jobs in Raleigh, NC (NOW HIRING)

UNC HEALTH

Director Clinical Research

Raleigh, NC · On-site

Provides strategic, operational, regulatory, financial, and program leadership for the Heart & Vascular clinical research portfolio. Directs program-level planning, workforce development, and ...

IQVIA

Clinical Research Associate

Durham, NC

$71K - $189K/yr

Clinical Research Associate II & Senior Clinical Research Associate (CRA II/Sr. CRA) Multiple ... May participate in study start-up activities, site budget tracking, financial management, and site ...

RemX

Be Seen First

Project Reconciliation Analyst - Clinical Research

Raleigh, NC · Remote

$60K - $70K/yr

Serve as the primary financial contact for assigned clinical research projects. * Review contracts, work orders, and amendments to identify financial terms and billing requirements. * Analyze project ...

IQVIA

Clinical Research Associate 2, IQVIA

Durham, NC · On-site

$71K - $189K/yr

IQVIA is hiring a Clinical Research Associate 2 with on-site monitoring experience in IM/GI, MASH ... If applicable, may be accountable for site financial management according to executed clinical ...

IQVIA

Clinical Research Associate 2, IQVIA

Durham, NC · On-site

$71K - $189K/yr

IQVIA is hiring a Clinical Research Associate 2 with on-site monitoring experience in IM/GI, MASH ... If applicable, may be accountable for site financial management according to executed clinical ...

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All JobsClinical Research Finance JobsClinical Research Finance Jobs in Raleigh, NC

Clinical Research Finance information

See Raleigh, NC salary details

$47.6K

$104.3K

$183.7K

How much do clinical research finance jobs pay per year?

As of Sep 5, 2026, the average yearly pay for clinical research finance in Raleigh, NC is $104,339.00, according to ZipRecruiter salary data. Most workers in this role earn between $78,700.00 and $119,100.00 per year, depending on experience, location, and employer.

What is clinical research finance?

Clinical research finance involves managing the financial aspects of clinical trials and research studies. This includes budgeting, billing, contract negotiation, financial compliance, and tracking study-related expenses. Professionals in this field ensure that research projects are properly funded, costs are allocated correctly, and all regulatory and sponsor requirements are met. Their work is critical to the successful and ethical operation of clinical research programs.

How does a clinical research finance professional typically collaborate with study coordinators and principal investigators during a clinical trial?

Clinical Research Finance professionals work closely with study coordinators and principal investigators to ensure accurate budgeting, timely invoicing, and compliance with sponsor requirements. They often participate in study start-up meetings to clarify financial processes, monitor ongoing expenses, and address budget variances. Effective collaboration helps to streamline financial reporting, ensure proper resource allocation, and facilitate smooth trial operations, ultimately supporting both the research team and institutional goals.

What are the key skills and qualifications needed to thrive in clinical research finance, and why are they important?

To excel in Clinical Research Finance, you need a solid grasp of financial management, budgeting, and clinical research protocols, often supported by a degree in finance, accounting, or a health-related field. Familiarity with clinical trial management systems (CTMS), financial tracking software, and compliance regulations such as NIH or FDA guidelines is typical. Strong analytical skills, attention to detail, and effective communication help professionals collaborate with research teams and sponsors. Mastery of these skills ensures accurate financial oversight, regulatory compliance, and successful support of clinical research objectives.

What is the difference between Clinical Research Finance vs Clinical Research Coordinator?

AspectClinical Research FinanceClinical Research Coordinator
Primary FocusManaging budgets, financial planning, and billing for clinical trialsOverseeing trial operations, patient recruitment, and data collection
Required CredentialsFinance or accounting background, certifications like CPA or CMA often preferredHealthcare or research-related education, often with clinical research certifications
Work EnvironmentFinance departments, research organizations, hospitalsResearch sites, hospitals, clinics
Employer & Industry UsagePharmaceutical companies, CROs, research institutionsAcademic medical centers, hospitals, research sites

Clinical Research Finance professionals focus on managing the financial aspects of clinical trials, ensuring budgets are maintained and billing is accurate. In contrast, Clinical Research Coordinators handle the day-to-day operations of trials, including patient interactions and data collection. Both roles are essential in the clinical research industry but serve different functions.

What are popular job titles related to Clinical Research Finance jobs in Raleigh, NC?

For Clinical Research Finance jobs in Raleigh, NC, the most frequently searched job titles are:

What job categories do people searching Clinical Research Finance jobs in Raleigh, NC look for?

The top searched job categories for Clinical Research Finance jobs in Raleigh, NC are:

What cities near Raleigh, NC are hiring for Clinical Research Finance jobs?

Cities near Raleigh, NC with the most Clinical Research Finance job openings:

Clinical Research Finance jobs near you
Infographic showing various Clinical Research Finance job openings in Raleigh, NC as of August 2026, with employment types broken down into 4% As Needed, 92% Full Time, and 4% Contract. Highlights an 70% In-person, 4% Hybrid, and 26% Remote job distribution, with an average salary of $104,339 per year, or $50.2 per hour.

Senior Clinical Research Coordinator

Velocity Clinical Research, Inc.

Raleigh, NC • On-site

$21.50 - $28.50/hr

Part-time

Medical, Dental, Vision, Retirement, PTO

This job post has expired 1 day ago. Applications are no longer accepted.

Velocity Clinical Research rating

7.3

Company rating: 7.3 out of 10

Based on 5 frontline employees who took The Breakroom Quiz

73rd of 121 rated laboratories

Job description

Overview
Velocity Clinical Research is an owned and integrated research site organization, providing excellence in patient care, high quality data and fully integrated research sites. At Velocity, we align our values and behaviors to give our employees the best chance of delivering on our brand promise: to bring innovative medical treatments to patients. We are committed to making clinical trials succeed by generating high quality data from as many patients as possible, as quickly as possible while providing exemplary patient care at every step.
As an employee of Velocity, you are the most integral part of our mission. For talented candidates who perform at a high level, Velocity will invest to support career advancement and reward performance. Whether you are new to clinical research or are an industry veteran, we invite you to apply to Velocity.
Benefits include medical, dental and vision insurance, paid time off and company holidays, 401(k) retirement plan with company-match, and an annual incentive program.
Summary:
Subject matter expert and leader of a clinical trial team to conduct and manage clinical trial(s) from start up through study close out in accordance with the study protocol, GCP, and Velocity's SOPs.
Responsibilities
Duties/Responsibilities:
  • Serve as leader of a study team to execute clinical trials
  • Mentor and train staff in the conduct of clinical trials, protocol requirements, communication,
    and trial management skills
  • Create training strategies and mitigation plans
  • Conduct and manage clinical trials in accordance with the study protocol, GCP, ICH Guidelines
    and Velocity's SOPs
  • Implement and coordinate assigned clinical trials including start up, vendor management,
    subject recruitment, source development review, scheduling subjects, protocol training,
    collection of regulatory documents, conducting visits, ensuring data is entered in a timely
    manner and all queries are resolved, managing and reporting adverse events, serious adverse
    events, and deviations, implementing new protocol amendments, providing all close out
    reports.
  • Apply project management concepts to manage risk and improve quality in the conduct of a
    clinical research study
  • Develop, coordinate, and implement research and administrative strategies to successfully
    manage assigned protocols.
  • Communicate effectively and professionally with coworkers, leadership, study subjects,
    sponsors, CROs, and vendors.
  • Ensure good documentation practices are applied by team members when collecting and
    correcting data, transferring data to sponsor/CRO data capture systems and resolving queries
  • Ensure confidentiality of patient protected health information, sponsor confidential information
    and Velocity confidential information is maintained by all team members
  • Develop communication and escalation strategies within teams to that ensure patient safety is
    upheld and all adverse events, serious adverse events, and adverse events of special interest
    are followed and reported in accordance with the protocol and Velocity SOPs
  • Ensure all data is entered into the sponsor's data portal and all queries are resolved in a timely
    manner
  • Ensure staff are delegated and trained appropriately and documented
  • Ensure the creation, collection and submission of regulatory documents to Sponsors and IRBs
    as required per protocol, GCP/ICH regulations and IRB requirements.
  • Evaluate potential subjects for participation in clinical trials including phone and in person pre screens.
  • Create and execute recruitment strategies in conjunction with patient recruitment staff
  • Incorporate key timelines, endpoints, required vendors, and patient population when planning
    for each assigned protocol.
  • Incorporate understanding of how decisions affect the bottom-line including links between
    operations and company's financial performance and how it is essential to create value of all
    stakeholders of the organization when planning for each assigned protocol.
  • Incorporate understanding of product development lifecycle and significance of protocol
    design including critical data points when planning for each assigned protocol
  • Develop Quality Control strategies for team member projects
  • Perform clinical duties (e.g. Drug preparation and administration, fibroscan, phlebotomy, ECG,
    lab processing) within scope
  • Promote respect for cultural diversity and conventions with all individuals.
  • Understand the disease process or condition under study
  • Other duties as assigned

Qualifications
Education/Experience:
  • Bachelor's degree and 4 years as a Clinical Research Coordinator OR
  • Associate's degree and 6 years as a Clinical Research Coordinator OR
  • High School Graduate and/or technical degree and 8 years as a Clinical Research Coordinator

Required Licenses/Certifications:
  • Phlebotomy if applicable and required by state law
    Intravenous/Intramuscular dose administration and preparation if applicable and required by state law
    Certified Clinical Research Coordinator through ACRP or SOCRA within six months of being in the role

Required Skills:
  • Advanced knowledge of medical terminology
  • Proficient in the use of the following technology: Computers, Microsoft Office software, fax, copier, and multi-line telephone.
  • Profcient ability to work in a fast-paced environment
  • Advanced verbal, written, and organizational skills
  • Advanced interpersonal and communication skills
  • Advanced ability to work as a team player
  • Advanced ability to read, write, and speak English
  • Demonstrated ability to multi-task
  • Advanced ability to follow written guidelines
  • Demonstrated ability to work independently, plan and prioritize multiple deliverables and objectives
  • Demonstrated ability to be flexible/adapt as daily schedule may change rapidly
  • Must be detail oriented
  • Proficient problem solving and strategic decision making ability.
  • Advanced in accepting individual responsibility for actions taken and demonstrating professionalism when judged, critiqued and/or praised.
  • Proficient leader, mentor and team builder

Required Physical Abilites:
  • Sit or stand for long periods of time
  • Travel locally and nationally
  • Communicate in person and by a telephone
  • Limited walking required
  • Limited to lifting up to 30 pounds

NOTE: The above Job Description is intended to communicate the general function of the mentioned position and by no means should be considered an exhaustive or complete outline of the specific tasks and functions that will be required. Additionally, specific tasks and duties of the position are subject to change as the Company, the department and circumstances change. All employees are expected to perform their duties within their ability as required by the job and/or as requested by management.

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