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Entry Level Clinical Study Startup Jobs in Raleigh, NC

Bruno

Clinical Payments Specialist

Raleigh, NC · On-site +1

Clinical Budget Specialist Clinical Research Location: Remote (United States) Employment Type ... Manage study-specific global investigator budget processes from study startup through closeout.

Bruno

Clinical Payments Specialist

Raleigh, NC · Remote

Clinical Budget Specialist Clinical Research Location: Remote (United States) Employment Type ... Manage study-specific global investigator budget processes from study startup through closeout.

Duke University

Clinical Research Coordinator

Durham, NC · On-site

$23.50 - $31.25/hr

Clinical Research Coordinator - Neurosurgery Research Be You. At Duke, we celebrate individuality ... Support study startup, feasibility assessments, ongoing project management, and study closeout ...

Duke University

Clinical Research Coordinator

Durham, NC · On-site

$23.50 - $31.25/hr

Clinical Research Coordinator - Neurosurgery Research Be You. At Duke, we celebrate individuality ... Support study startup, feasibility assessments, ongoing project management, and study closeout ...

Duke University

READING CENTER PROJECT MGR.

Durham, NC

$23.06 - $34.96/hr

... clinical trial data, images, and study-related activities. What You'll Do: * This position will ... study startup and site certification activities * Track, confirm, and document receipt of all ...

Duke University

READING CENTER PROJECT MGR.

Durham, NC · On-site

$23.06 - $34.96/hr

... clinical trial data, images, and study-related activities. What You'll Do: * This position will ... study startup and site certification activities * Track, confirm, and document receipt of all ...

Duke University

READING CENTER PROJECT MGR.

Durham, NC · On-site

$23.06 - $34.96/hr

... clinical trial data, images, and study-related activities. What You'll Do: * This position will ... study startup and site certification activities * Track, confirm, and document receipt of all ...

Duke University

READING CENTER PROJECT MGR.

Durham, NC

$23.06 - $34.96/hr

... clinical trial data, images, and study-related activities. What You'll Do: * This position will ... study startup and site certification activities * Track, confirm, and document receipt of all ...

Duke University

READING CENTER PROJECT MGR.

Durham, NC · On-site

$23.06 - $34.96/hr

... clinical trial data, images, and study-related activities. What You'll Do: * This position will ... study startup and site certification activities * Track, confirm, and document receipt of all ...

Duke University

READING CENTER PROJECT MGR.

Durham, NC · On-site

$23.06 - $34.96/hr

... clinical trial data, images, and study-related activities. What You'll Do: * This position will ... study startup and site certification activities * Track, confirm, and document receipt of all ...

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All JobsClinical Study Startup JobsEntry Level Clinical Study Startup JobsEntry Level Clinical Study Startup Jobs in Raleigh, NC

Entry Level Clinical Study Startup information

See Raleigh, NC salary details

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How much do entry level clinical study startup jobs pay per hour?

As of Aug 3, 2026, the average hourly pay for entry level clinical study startup in Raleigh, NC is $36.62, according to ZipRecruiter salary data. Most workers in this role earn between $25.00 and $46.73 per hour, depending on experience, location, and employer.

What is the difference between Entry Level Clinical Study Startup vs Clinical Research Coordinator?

AspectEntry Level Clinical Study StartupClinical Research Coordinator
CredentialsBachelor's degree, training in clinical trial processesBachelor's degree, often with certification in clinical research
Work EnvironmentPrepares sites, manages startup documentation, coordinates with teamsOversees patient recruitment, data collection, and site activities
Employer & IndustryPharmaceutical companies, CROs, biotech firmsHospitals, clinics, research institutions

Entry Level Clinical Study Startup roles focus on preparing clinical sites for trials, including documentation and regulatory submissions. Clinical Research Coordinators manage patient interactions and data during the trial. Both roles require similar educational backgrounds but differ in daily responsibilities and focus areas within the clinical research process.

What are the most commonly searched types of Clinical Study Startup jobs in Raleigh, NC? The most popular types of Clinical Study Startup jobs in Raleigh, NC are:
What are popular job titles related to Entry Level Clinical Study Startup jobs in Raleigh, NC? For Entry Level Clinical Study Startup jobs in Raleigh, NC, the most frequently searched job titles are:
What job categories do people searching Entry Level Clinical Study Startup jobs in Raleigh, NC look for? The top searched job categories for Entry Level Clinical Study Startup jobs in Raleigh, NC are:
What cities near Raleigh, NC are hiring for Entry Level Clinical Study Startup jobs? Cities near Raleigh, NC with the most Entry Level Clinical Study Startup job openings:
Entry Level Clinical Study Startup jobs near you
Infographic showing various Entry Level Clinical Study Startup job openings in Raleigh, NC as of July 2026, with employment types broken down into 2% As Needed, 74% Full Time, 17% Part Time, and 7% Contract. Highlights an 95% Physical, 1% Hybrid, and 4% Remote job distribution, with an average salary of $76,160 per year, or $36.6 per hour.

Clinical Payments Specialist

Bruno

Raleigh, NC • On-site, Remote

Full-time

Posted 18 days ago

Job description

Clinical Budget Specialist Clinical Research
Location: Remote (United States)
Employment Type: Full-Time
Our client is seeking a Budget Operations Specialist to support global clinical trial operations by managing investigator budgets, site setup, and payment-related data throughout the lifecycle of clinical studies. This role is ideal for a detail-oriented professional with experience in clinical research, investigator budgets, contracts, and site payment operations.
The successful candidate will play a key role in ensuring accurate budget setup, maintaining study data, and collaborating with sponsors, CROs, and investigative sites to support efficient clinical trial execution.
Key Responsibilities
  • Manage study-specific global investigator budget processes from study startup through closeout.
  • Review and reconcile study budgets, contracts, amendments, payment schedules, protocols, and related documentation.
  • Set up investigative sites and maintain study information within the organization's clinical payment platform.
  • Enter and maintain baseline study budgets, site-specific budgets, budget amendments, and payee information.
  • Ensure investigator budgets align with Clinical Trial Agreements and protocol amendments.
  • Respond to budget-related inquiries from sponsors, CROs, and investigative sites.
  • Research and resolve budget discrepancies and data issues in a timely manner.
  • Maintain accurate study documentation and payment-related records.
  • Develop and maintain strong relationships with internal teams, sponsors, CROs, and investigative sites.
  • Stay current on study changes, contract updates, and protocol amendments that impact budgets and payments.
  • Support additional operational projects and responsibilities as assigned.
Qualifications
  • Bachelor's degree or equivalent combination of education and experience.
  • Minimum of 2 years of experience in clinical research, biopharmaceuticals, or a related healthcare environment.
  • Experience working with investigator contracts, study budgets, and/or site payment operations.
  • Understanding of protocol amendments and their impact on investigator budgets, subject visits, contracts, and payment schedules.
  • Advanced proficiency in Microsoft Excel and working knowledge of Microsoft Word, Outlook, and SharePoint.
  • Strong organizational and time management skills with exceptional attention to detail.
  • Ability to quickly learn new systems and adapt to changing technologies and processes.
  • Self-motivated with the ability to work independently while collaborating effectively within a team.
  • Strong written and verbal communication skills with a professional client-facing approach.
  • Excellent proofreading skills with the ability to identify mathematical, grammatical, and documentation errors.
  • Basic understanding of accounting and budgeting principles is preferred.
Why Apply?
  • 100% Remote (U.S.)
  • Join a growing organization supporting global clinical research.
  • Opportunity to work with sponsors and clinical research organizations on high-impact studies.
  • Collaborative team environment with opportunities for professional growth.
Application
Please submit your resume for consideration. Qualified candidates will be contacted to discuss the opportunity in more detail.

Apply