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Remote Senior Clinical Research Associate Jobs in Raleigh, NC

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 ...

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 ...

Senior Proposals Writer - United States, Remote ICON is a global healthcare intelligence and clinical research organisation united by a mission to bring new medicines and treatments to patients ...

Clinical Project Lead, Oncology

Durham, NC ยท Remote

$68K - $232K/yr

In this remote role you will serve as the primary country-level leader for clinical trial delivery ... clinical research. Key Responsibilities Clinical Trial Delivery & Oversight * Lead end-to-end ...

Clinical Project Lead, Oncology

Durham, NC ยท Remote

$68K - $232K/yr

In this remote role you will serve as the primary country-level leader for clinical trial delivery ... clinical research. Key Responsibilities Clinical Trial Delivery & Oversight * Lead end-to-end ...

Showing results 41-60

Remote Senior Clinical Research Associate information

See Raleigh, NC salary details

$35K

$91.7K

$139.5K

How much do remote senior clinical research associate jobs pay per year?

As of Aug 4, 2026, the average yearly pay for remote senior clinical research associate in Raleigh, NC is $91,681.00, according to ZipRecruiter salary data. Most workers in this role earn between $60,800.00 and $124,400.00 per year, depending on experience, location, and employer.

What is a remote senior clinical research associate?

A Remote Senior Clinical Research Associate (CRA) is a highly experienced professional who oversees and monitors clinical trials, ensuring they are conducted according to regulatory guidelines, protocols, and good clinical practice (GCP) standards, all while working remotely. Senior CRAs are responsible for site management, data verification, and ensuring participant safety and data integrity. They typically act as the main point of contact between the sponsor and the clinical trial sites, and may also mentor or train junior staff. Working remotely allows them to manage multiple sites across different locations more efficiently. This role requires strong communication, organizational, and analytical skills, as well as extensive clinical research experience.

What are the key skills and qualifications needed to thrive as a remote senior clinical research associate?

To thrive as a Remote Senior Clinical Research Associate, you need expertise in clinical trial management, regulatory compliance, and a background in life sciences, often supported by a bachelor's degree and several years of CRA experience. Familiarity with electronic data capture (EDC) systems, ICH-GCP guidelines, and certifications like ACRP or SOCRA are commonly required. Strong organizational skills, attention to detail, and excellent communication are crucial for managing trials remotely and ensuring protocol adherence. These skills are vital to maintaining data integrity, regulatory compliance, and successful study outcomes across geographically dispersed sites.

What is the difference between Remote Senior Clinical Research Associate vs Remote Clinical Research Associate?

AspectRemote Senior Clinical Research AssociateRemote Clinical Research Associate
Required CredentialsBachelor's degree, clinical research experience, often some certificationBachelor's degree, entry-level experience, often similar certifications
Work EnvironmentRemote, overseeing multiple sites, higher responsibilityRemote, supporting clinical trials, more focused on data collection
Employer & Industry UsagePharmaceutical companies, CROs, biotech firmsSimilar employers, often entry-level or supporting roles
Search & Comparison IntentUnderstanding senior roles, career progressionEntry-level understanding, role clarification

The Remote Senior Clinical Research Associate typically has more experience, greater responsibilities, and oversees multiple sites remotely. The Remote Clinical Research Associate is often an entry-level or supporting role focused on data collection and site support. Both roles are essential in clinical trials, but the senior position involves higher oversight and decision-making.

What are some common challenges faced by remote senior clinical research associates, and how can they be managed?

Remote Senior Clinical Research Associates often face challenges related to maintaining effective communication with site staff and sponsors, as well as ensuring protocol compliance without frequent on-site visits. To manage these, it's important to leverage digital monitoring tools, schedule regular virtual check-ins, and develop strong organizational habits for tracking site progress. Building trusting relationships with site teams and being proactive in addressing issues can also help ensure studies stay on track, even when working remotely.
What are popular job titles related to Remote Senior Clinical Research Associate jobs in Raleigh, NC? For Remote Senior Clinical Research Associate jobs in Raleigh, NC, the most frequently searched job titles are:
What job categories do people searching Remote Senior Clinical Research Associate jobs in Raleigh, NC look for? The top searched job categories for Remote Senior Clinical Research Associate jobs in Raleigh, NC are:
What cities near Raleigh, NC are hiring for Remote Senior Clinical Research Associate jobs? Cities near Raleigh, NC with the most Remote Senior Clinical Research Associate job openings:
Infographic showing various Remote Senior Clinical Research Associate job openings in Raleigh, NC as of July 2026, with employment types broken down into 100% Full Time. Highlights an 100% Remote job distribution, with an average salary of $91,681 per year, or $44.1 per hour.

Clinical Payments Specialist

Bruno

Raleigh, NC โ€ข On-site, Remote

Full-time

Posted 19 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.