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Remote Clinical Sme Jobs (NOW HIRING)

This is a remote position so the candidate can live anywhere in the USA. The position will require ... clinical trials, forensics, medical device, pharmaceutical, public health and research hospitals ...

Hands-on Technical SME with deep implementation experience in FHIR-based healthcare ... The ideal candidate is an engineer-first practitioner who understands clinical workflows, has ...

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Remote Clinical Sme information

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$14

$34

$90

How much do remote clinical sme jobs pay per hour?

As of Jun 11, 2026, the average hourly pay for remote clinical sme in the United States is $34.62, according to ZipRecruiter salary data. Most workers in this role earn between $16.59 and $32.93 per hour, depending on experience, location, and employer.

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

AspectRemote Clinical SmeRemote Clinical Research Associate
CredentialsTypically requires clinical expertise, certifications like CCRP or RACRequires clinical research experience, GCP training, and often a degree in life sciences
Work EnvironmentCollaborates with cross-functional teams, provides subject matter expertiseMonitors clinical trials, ensures compliance, and manages trial data
Industry UsageUsed in pharmaceutical, biotech, and healthcare companies for expert consultationCommonly employed in clinical trial sites and CROs for trial oversight
Search & Comparison IntentOften compared for clinical expertise roles in trialsCompared for trial monitoring and compliance roles

The Remote Clinical Sme focuses on providing expert clinical knowledge and consultation within healthcare and biotech companies, while the Remote Clinical Research Associate primarily oversees and monitors clinical trials to ensure compliance and data integrity. Both roles require clinical experience but differ in daily responsibilities and focus areas.

What is a Remote Clinical SME?

A Remote Clinical Subject Matter Expert (SME) is a healthcare professional with specialized knowledge in a specific clinical field who provides expertise, guidance, and consultation from a remote location. They often assist with tasks such as reviewing medical content, advising on clinical guidelines, supporting product development, or training staff—all without being physically present. Remote Clinical SMEs are crucial for organizations that require expert input but do not need full-time, on-site clinical staff. Their work is commonly utilized by healthcare companies, educational institutions, and technology firms developing medical products.

What are the key skills and qualifications needed to thrive as a Remote Clinical SME, and why are they important?

To thrive as a Remote Clinical Subject Matter Expert (SME), you need advanced clinical expertise, relevant healthcare credentials (such as RN, MD, or PharmD), and extensive experience in your specialty area. Proficiency with telehealth platforms, electronic health records (EHRs), and collaboration tools like Zoom or Microsoft Teams is typically required. Strong communication, problem-solving, and self-management skills are essential for effectively sharing knowledge and working independently. These skills enable SMEs to provide accurate guidance, support remote teams, and ensure high-quality clinical outcomes in virtual environments.

How does a Remote Clinical SME typically collaborate with cross-functional teams in a virtual setting?

As a Remote Clinical Subject Matter Expert (SME), you'll frequently work with clinical operations, regulatory affairs, data management, and technology teams through virtual meetings, collaborative platforms, and shared documentation. Effective communication and timely feedback are crucial, as you'll be relied upon for your clinical expertise during project planning, protocol development, and review processes. Remote SMEs often use project management tools and video conferencing to stay connected, ensuring their insights are integrated into broader team objectives while maintaining flexibility and work-life balance.
More about Remote Clinical Sme jobs
What cities are hiring for Remote Clinical Sme jobs? Cities with the most Remote Clinical Sme job openings:
What are the most commonly searched types of Clinical Sme jobs? The most popular types of Clinical Sme jobs are:
What states have the most Remote Clinical Sme jobs? States with the most job openings for Remote Clinical Sme jobs include:
Infographic showing various Remote Clinical Sme job openings in the United States as of June 2026, with employment types broken down into 88% Full Time, 6% Part Time, and 6% Contract. Highlights an 100% Remote job distribution, with an average salary of $72,002 per year, or $34.6 per hour.
Business Analyst Veeva Vault Clinical (CTMS/eTMF) - Remote - Full time

Business Analyst Veeva Vault Clinical (CTMS/eTMF) - Remote - Full time

Lorven Technologies

Remote

Full-time

Posted 21 days ago


Job description

Our client seeks an Business Analyst Veeva Vault Clinical (CTMS/eTMF) for a Full Time Project in Remote . Below is the detailed requirement
Job Title: Business Analyst Veeva Vault Clinical (CTMS/eTMF)
Work location : Remote
Duration: Full Time
Job Description:
  • Bachelor's degree preferably in Computer Science, Information technology, Computer Engineering, or related IT discipline or equivalent experience with 12+ Minimum Experience

Skills & Experience
  • Business Analyst with 10-12+ years of experience delivering or leading regulated enterprise or clinical systems initiatives
  • Hands-on experience with Veeva Vault Clinical (CTMS and eTMF)
  • Strong understanding of clinical trial operations and clinical systems workflows
  • Strong technical fluency to partner effectively with internal and external teams in Business, IT, Data, Infrastructure, and QA
  • Demonstrated experience overseeing release and environment management in a GxP-regulated environment
  • Proven ability to lead complex, cross-functional initiatives and drive clarity from ambiguity
  • Excellent executive communication, documentation, and stakeholder management skills

Business Analysis Leadership/Execution & Veeva Vault Clinical Expertise
  • Lead complex, cross-functional initiatives related to Veeva Vault Clinical (CTMS/eTMF), including implementation, optimization efforts, migrations, and strategic enhancements
  • Convert ambiguity into clear problem statements, scope, success criteria, execution plans, timelines, risks, and decision points
  • Proactively manage dependencies, trade-offs, and risks; elevate decisions with clear recommendations to Clinical Systems LT
  • Serve as a SME for Veeva Vault Clinical (CTMS/eTMF), advising on configuration implications, functional capabilities, and downstream system impacts
  • Partner with development and support teams on complex or systemic issues, contributing to root-cause analysis and long-term solutions
  • Participate in enhancement definition, prioritization, solution design, and validation strategy
  • Collaborate closely with integration and data teams on end-to-end clinical system workflows
  • Review key technical and functional documentation, including business and system requirements, design specifications, release notes, validation plans, and SOPs
  • Ensure documentation is complete, accurate, and aligned with intended business outcomes, system behavior, and regulatory expectations
  • Act as a translator between technical and business audiences, validating that documentation clearly reflects scope, assumptions, risks, and downstream impacts
  • Partner with CS Leads, QA, Val, and IT to ensure documentation supports validation, inspection readiness, and audit traceability

Migration and Transformation Leadership -- Lead/contribute to large-scale system migration, of Client legacy CTMS Gilda (Siebel) to Veeva Vault Clinical and related transformation efforts; Drive/participate in migration planning, including cutover strategy, data validation approach, reconciliation methods, rollback planning, communications, change management, and archiving strategy; Help to coordinate technical and business readiness across all stakeholder groups
Validation, Compliance, Release and Environment Management -- Provide oversight and coordination for Veeva Vault Clinical releases across non-production and production environments; As needed, partner with QA, Val, and IT to ensure delivery aligns with GxP and validation expectations; Drive release impact assessments, cross-functional readiness reviews, and deployment sequencing in partnership with IT, QA, Val and development teams; Ensure appropriate governance and usage of development, test, and UAT environments to support parallel workstreams and testing cycles; Act as a single point of orchestration for release- and environment-related dependencies, risks, and conflicts; Ensure releases are executed in a compliant, predictable, and business-aligned manner; Provide oversight and contribution to validation approaches, UAT strategy, and release documentation
Executive Communication and Clinical Systems Leadership Enablement -- Operate as a trusted advisor and analyst for Clinical Systems LT; Lead routine internal Clinical Systems Meeting to ensure internal alignment on technical and operational decisions/risks/updates on the Vault Clinical program; Deliver concise, executive-ready communication on progress, risks, trade-offs, and decisions required; Influence with minimal oversight to gain alignment and drive outcomes across senior stakeholder groups
Preferred / Nice-to-haves
  • Experience with system integrations (e.g., CTMS ↔ eTMF/EDC/Data Lakes & repositories)
  • Experience working with Siebel (CTMS), working with Veeva Managed Services or vendor escalations
  • Familiarity with Agile or DevOps methodologies; Knowledge of clinical metrics and reporting tools
  • Siebel CTMS experience, particularly in migration or decommissioning efforts
  • Experience with system integrations, APIs, middleware, and data platforms
  • Experience with Veeva Managed Services or external vendors
  • Exposure to operational metrics, reporting, or analytics in a clinical systems setting

Lorven technologies logo

About Lorven technologies

Sourced by ZipRecruiter

Lorven Technologies, headquartered in Plainsboro, New Jersey, United States, is a reputable company in the technology industry, specializing in providing effective IT solutions and consulting services. The company's official website, lorventech.com, offers comprehensive insights into its offerings which include but are not limited to software development, IT consulting, project management, and business analysis. Since its inception, Lorven Technologies has been committed to ensuring efficiency and reliability in delivering IT services to its global clientele, establishing itself as a trusted name in the industry.

Industry

It services

Company size

51 - 200 Employees

Headquarters location

Plainsboro, NJ, US

Year founded

2001

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