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Remote Clinical Study Startup Jobs in Raleigh, NC

Bruno

Clinical Payments Specialist

Raleigh, NC · On-site +1

Remote (United States) Employment Type: Full-Time Our client is seeking a Budget Operations ... Manage study-specific global investigator budget processes from study startup through closeout.

Bruno

Clinical Payments Specialist

Raleigh, NC · Remote

Remote (United States) Employment Type: Full-Time Our client is seeking a Budget Operations ... Manage study-specific global investigator budget processes from study startup through closeout.

Trilogy

Senior/Principal Medical Writer - USA

Durham, NC · On-site +1

$120K - $159K/yr

... in office/remote) from our Durham, NC, USA office. You willbe responsible for: * Preparinga variety of clinical regulatory documents (Clinical Study Protocols, Clinical Study Reports, Clinical ...

IQVIA

Clinical Research Coordinator

Raleigh, NC · Remote

$35 - $42/hr

Perform study-related clinical procedures, including ECGs, vital signs, specimen collection, and ... This position is not eligible for employment sponsorship. #LI-CES and #LI-DNP #LI-HCP #remote IQVIA ...

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Remote Clinical Study Startup information

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How much do remote clinical study startup jobs pay per hour?

As of Aug 5, 2026, the average hourly pay for remote clinical study startup in Raleigh, NC is $60.77, according to ZipRecruiter salary data. Most workers in this role earn between $49.33 and $68.46 per hour, depending on experience, location, and employer.

What is a remote clinical study startup?

A Remote Clinical Study Startup refers to the initial phase of setting up clinical trials, conducted primarily through digital tools and remote processes. This includes activities like site identification, regulatory submissions, contract negotiations, and ethics approvals, all managed without requiring in-person meetings. Remote startups leverage technology to streamline processes, reduce timelines, and improve collaboration among stakeholders. This approach is especially useful for multi-site studies or when in-person interactions are limited by geography or global events.

What is the difference between Remote Clinical Study Startup vs Remote Clinical Trial Coordinator?

AspectRemote Clinical Study StartupRemote Clinical Trial Coordinator
Primary RolePlanning and initiating clinical studies, including site selection and regulatory submissionsManaging daily trial activities, site communication, and data collection
Required CredentialsTypically a background in life sciences, clinical research certifications preferredSimilar credentials, often with clinical research or coordinator certifications
Work EnvironmentPrimarily remote, collaborating with sponsors, CROs, and sitesRemote or hybrid, focusing on site management and data oversight
Industry UsageUsed during study initiation phaseUsed during trial execution phase

Remote Clinical Study Startup involves planning and launching new clinical trials, while Remote Clinical Trial Coordinator focuses on managing ongoing trial activities. Both roles require similar credentials and often operate remotely within the clinical research industry, but they differ in their specific responsibilities and timing within the study lifecycle.

What are the key skills and qualifications needed to thrive as a remote clinical study startup specialist?

To thrive as a Remote Clinical Study Startup Specialist, you need a solid understanding of clinical trial processes, regulatory requirements, and project management, usually supported by a degree in life sciences or a related field. Familiarity with clinical trial management systems (CTMS), electronic trial master files (eTMF), and regulatory submission platforms is essential. Strong organizational skills, attention to detail, and effective communication are vital soft skills for coordinating teams and ensuring timely study activation. These skills and qualities are crucial for maintaining compliance, minimizing delays, and driving successful clinical trial launches in a remote environment.

What are some common challenges faced in a remote clinical study startup role, and how can they be addressed?

Professionals in Remote Clinical Study Startup roles often encounter challenges such as coordinating documentation across multiple sites, ensuring regulatory compliance in different regions, and maintaining clear communication among dispersed teams. Successfully overcoming these hurdles typically involves leveraging robust digital tools for project management and document tracking, as well as establishing standardized communication protocols. Proactive problem-solving and strong organizational skills are essential for keeping timelines on track and ensuring all study startup activities are completed efficiently.
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 Remote Clinical Study Startup jobs in Raleigh, NC? For Remote Clinical Study Startup jobs in Raleigh, NC, the most frequently searched job titles are:
What job categories do people searching Remote Clinical Study Startup jobs in Raleigh, NC look for? The top searched job categories for Remote Clinical Study Startup jobs in Raleigh, NC are:
What cities near Raleigh, NC are hiring for Remote Clinical Study Startup jobs? Cities near Raleigh, NC with the most Remote Clinical Study Startup job openings:
Remote Clinical Study Startup jobs near you

Clinical Payments Specialist

Bruno

Raleigh, NC • On-site, Remote

Full-time

Posted 20 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