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Remote Pfizer Clinical Research 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 ...

We are looking for a Clinical Trial Leader (CTL) to join our A-team (office-based*/remote). As a CTL at Allucent, you are providing leadership, management and oversight to the Clinical Research ...

We are looking for a Clinical Trial Leader (CTL) to join our A-team (office-based*/remote). As a CTL at Allucent, you are providing leadership, management and oversight to the Clinical Research ...

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 ...

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 ...

We are looking for a Clinical Trial Leader (CTL) to join our A-team (office-based*/remote). As a CTL at Allucent, you are providing leadership, management and oversight to the Clinical Research ...

... remote). This position will involve analyzing patient data and coordinating analysis of patient ... Manage, store, and analyze clinical research data Conduct systematic literature reviews, develop ...

Showing results 21-40

Remote Pfizer Clinical Research information

See Raleigh, NC salary details

$35K

$91.7K

$139.5K

How much do remote pfizer clinical research jobs pay per year?

As of Aug 10, 2026, the average yearly pay for remote pfizer clinical research 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 remote Pfizer clinical research?

Remote Pfizer clinical research jobs involve supporting or conducting clinical trials and research studies for Pfizer while working from a location outside of a traditional office or clinical site. These roles can encompass tasks such as data management, clinical monitoring, regulatory documentation, and coordinating trial activities virtually. Remote positions offer flexibility and the ability to collaborate with global teams, while still ensuring adherence to regulatory standards and study protocols. Candidates typically need experience in clinical research and strong communication and organizational skills.

What is the difference between Remote Pfizer Clinical Research vs Remote Clinical Data Coordinator?

AspectRemote Pfizer Clinical ResearchRemote Clinical Data Coordinator
Required CredentialsBachelor's degree in health sciences, clinical research certification often preferredBachelor's degree in health or related field, data management training
Work EnvironmentRemote, within pharmaceutical or clinical research settingsRemote, focused on data entry and management
Employer & IndustryPfizer, pharmaceutical/biotech industryHealthcare organizations, research sites, or CROs
Common Search & ComparisonYesYes

Remote Pfizer Clinical Research roles involve overseeing clinical trials, ensuring compliance, and working within pharmaceutical companies. Remote Clinical Data Coordinators focus on managing and entering clinical trial data, often within research sites or CROs. Both roles require related certifications and work in the clinical research industry, but they differ in responsibilities and daily tasks.

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

To thrive as a Remote Pfizer Clinical Research professional, you need a background in life sciences or a related field, experience in clinical research, and often a relevant certification such as CCRA or SOCRA. Familiarity with electronic data capture (EDC) systems, clinical trial management systems (CTMS), and Good Clinical Practice (GCP) guidelines is typically required. Strong analytical thinking, attention to detail, and excellent written and verbal communication skills set top candidates apart. These skills ensure the integrity, compliance, and effectiveness of clinical trials conducted remotely to advance medical research.

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

Remote Pfizer clinical research professionals often encounter challenges related to communication and coordination with cross-functional teams, as research projects typically involve colleagues from multiple departments and time zones. Maintaining data integrity and ensuring compliance with regulatory standards can also be more complex when working remotely. To manage these challenges, it's important to leverage collaborative digital platforms, establish clear communication protocols, and participate in regular virtual meetings. Additionally, staying up-to-date with company training and guidelines helps ensure that all research activities align with Pfizer’s high standards and regulatory requirements.
What are the most commonly searched types of Pfizer Clinical Research jobs in Raleigh, NC? The most popular types of Pfizer Clinical Research jobs in Raleigh, NC are:
What are popular job titles related to Remote Pfizer Clinical Research jobs in Raleigh, NC? For Remote Pfizer Clinical Research jobs in Raleigh, NC, the most frequently searched job titles are:
What cities near Raleigh, NC are hiring for Remote Pfizer Clinical Research jobs? Cities near Raleigh, NC with the most Remote Pfizer Clinical Research job openings:
Infographic showing various Remote Pfizer Clinical Research job openings in Raleigh, NC as of August 2026, with employment types broken down into 64% Full Time, 18% Part Time, 9% Temporary, and 9% Contract. 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 • Remote

Full-time

Posted 24 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.