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Remote Clinical Data Reviewer Jobs in Tennessee (NOW HIRING)

Remote Clinical Coder and Quality Review for the Home Care division. Line of Authority: Director of ... Typing and data entry proficiency * Web-based application experience * OASIS review and instruction

Remote Clinical Coder and Quality Review for the Home Care division. Line of Authority: Director of ... Typing and data entry proficiency * Web-based application experience * OASIS review and instruction

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Remote Clinical Data Reviewer information

What is a remote clinical data reviewer?

Remote Clinical Data Reviewers are professionals who analyze and validate clinical trial data from a remote location, ensuring its accuracy and compliance with regulatory standards. They play a crucial role in identifying discrepancies, data entry errors, and protocol deviations in clinical studies. By collaborating with study teams and using electronic data capture systems, they help maintain data integrity and support the successful completion of clinical research projects. This position allows for flexible work arrangements, as the tasks can be performed from home or any location with secure internet access.

What skills and qualifications are needed to be a remote clinical data reviewer?

To thrive as a Remote Clinical Data Reviewer, you need a strong background in life sciences or a related field, experience with clinical trial processes, and a keen eye for detail. Familiarity with clinical data management systems (CDMS), electronic data capture (EDC) platforms, and knowledge of GCP (Good Clinical Practice) guidelines or relevant certifications are typically required. Strong analytical skills, effective written communication, and time management are important soft skills for success in this role. These skills ensure accurate data validation, regulatory compliance, and efficient remote collaboration to support high-quality clinical research outcomes.

What are common challenges faced by remote clinical data reviewers and how can they be managed?

Remote Clinical Data Reviewers often face challenges such as ensuring data accuracy across different electronic data capture systems, maintaining effective communication with on-site teams, and managing time zone differences. To manage these challenges, it’s important to establish clear protocols for data verification, utilize collaborative tools for real-time communication, and adhere to a structured workflow and regular check-ins with the broader project team. Proactively seeking clarification and staying updated with protocol amendments also help ensure high-quality data review from a remote setting.

What is the difference between Remote Clinical Data Reviewer vs Remote Clinical Data Coordinator?

AspectRemote Clinical Data ReviewerRemote Clinical Data Coordinator
CredentialsTypically requires a degree in life sciences, health informatics, or related field; certifications like CDISC or CDM are commonSimilar credentials; often holds degrees in health sciences or related fields; certifications may include clinical trial management
Work EnvironmentPrimarily reviews and validates clinical data, often working independently or in small teamsCoordinates data collection, manages databases, and communicates with sites and teams
Employer & Industry UsageUsed by pharmaceutical companies, CROs, and biotech firms for data quality assuranceEmployed by similar organizations to oversee data flow and trial documentation

The main difference is that Remote Clinical Data Reviewers focus on analyzing and validating clinical data, while Remote Clinical Data Coordinators handle data management and coordination tasks. Both roles require similar educational backgrounds and are integral to clinical trial processes, but their daily responsibilities differ significantly.

What cities in Tennessee are hiring for Remote Clinical Data Reviewer jobs?

Cities in Tennessee with the most Remote Clinical Data Reviewer job openings:

Infographic showing various Remote Clinical Data Reviewer job openings in Tennessee as of June 2026, with employment types broken down into 87% Full Time, 11% Part Time, 1% Contract, and 1% Nights. Highlights an 86% Physical, 4% Hybrid, and 10% Remote job distribution.

Director, Clinical Data & AI

SMITH & NEPHEW SNATS INC

Memphis, TN • On-site, Remote

Full-time

Medical, Dental, Vision, Retirement, PTO

Re-posted 7 days ago


Job description

Life Unlimited. At Smith+Nephew we design and manufacture technology that takes the limits off living. The Director of Clinical Data & AI is the global functional leader responsible for the strategy, architecture, and operational execution of clinical data and AI capabilities supporting end-to-end evidence generation. This role owns the clinical data lifecycle-from data acquisition and management to advanced analytics, AI enablement, and synthetic/simulated data-ensuring all data assets are high-quality, interoperable, and fit-for-purpose for regulatory, scientific, and operational decision-making. The Director serves as the enterprise authority on clinical data platforms and AI-enabled evidence generation, driving integration across clinical systems, data engineering, AI/ML, and statistical/clinical programming. This position has full accountability for the strategy, execution, quality, and evolution of the Clinical Data & AI function globally.

What will you be doing?

1. Global Clinical Data & AI Strategy

  • Define and execute the global strategy for Clinical Data & AI aligned to enterprise evidence-generation and AI transformation goals
  • Establish a unified operating model integrating:
    • Clinical systems (EDC, eCOA, registries)
    • Clinical Data Lake & central data model
    • Data management and data engineering
    • AI/ML and advanced analytics
  • Serve as the enterprise authority on clinical data architecture and AI enablement for clinical & medical affairs across all BUs and geographies
  • Partner with Clinical Study Management, Clinical Strategy, Regulatory, Medical Affairs, Statistics, and IT to define data-driven evidence strategies

2. Clinical Data Architecture & Platforms

  • Own the design, governance, and evolution of:
    • Clinical Data Lake (CDL) and standardized data models
    • Clinical systems ecosystem (EDC, eCOA, registry ingestion, integrations)
    • Data pipelines, transformation, and interoperability frameworks
  • Ensure scalable, compliant, and extensible architecture supporting:
    • Cross-study analytics
    • Real-world data integration
    • Device + clinical data linkage
  • Drive standardization (e.g., CDISC-based models) and elimination of data silos

3. AI, Data Science & Advanced Analytics

  • Lead development and deployment of AI/ML capabilities across the clinical lifecycle, including:
    • Data quality automation and monitoring
    • AI-assisted clinical study reporting and analytics
    • Cross-study insights and meta-analyses
  • Drive integration of AI into core workflows, not point solutions
  • Establish best practices for:
    • Model development, validation, monitoring
    • Responsible AI (traceability, reproducibility, regulatory alignment)
  • Oversee collaboration between data science, statistics, and programming teams

4. Synthetic Data, Simulation & Virtual Twins

  • Own strategy and execution for:
    • Synthetic clinical data generation
    • Simulation frameworks for study design and operational planning
    • Virtual twin development for patient- and study-level modeling
  • Ensure alignment with regulatory expectations for transparency and scientific validity
  • Integrate synthetic and simulated data into:
    • Study design optimization
    • Evidence generation (e.g., hybrid designs, external controls)

5. Clinical Data Management & Quality

  • Oversee global clinical data management function, ensuring:
    • High-quality, consistent, and inspection-ready data
    • Efficient study startup (eCRF design, database builds) and closeout
    • Risk-based monitoring and analytics-driven data review
  • Embed AI, machine learning modeling, and automation into CDM workflows to improve efficiency and quality
  • Ensure alignment with regulatory and compliance standards (FDA, EU MDR, GDPR, HIPAA)

6. Statistical & Clinical Programming Integration

  • Own alignment and integration of:
    • Statistical programming (TFLs, ADaM outputs)
    • Clinical programming (data pipelines, transformations)
  • Ensure seamless data flow from raw data analysis-ready datasets reporting
  • Drive standardization, automation, and reuse across studies and programs
  • Leverage AI solutions to accelerate programming across Global Clinical and Medical Affairs

7. Operational Excellence & Delivery Model

  • Own intake, prioritization, and delivery across:
    • Data platform initiatives
    • AI/ML programs
    • Study-level data operations
  • Implement scalable delivery models for standardized multi-source clinical outcomes datasets from the Clinical Data Lake to key business stakeholder teams
  • Optimize resourcing across:
    • High-throughput standardized work
    • High-complexity AI/data science initiatives

8. Regulatory & Data Governance Leadership

  • Ensure all clinical data and AI activities are:
    • Compliant with global regulatory requirements
    • Traceable, auditable, and reproducible
  • Establish strong governance across:
    • Data standards and lineage
    • AI model lifecycle
    • Data privacy and security
  • Support regulatory submissions with robust, defensible data strategies

Key Interfaces

  • Global Clinical Research Operations leadership
  • Clinical / Medical Affairs / Regulatory Affairs
  • Statistics, Data Science, and AI teams
  • IT / Digital / Enterprise Data organizations
  • External partners, CROs, AI vendors, and regulators

Education

  • BA required, PhD (preferred) or Master's in Data Science, Biostatistics, Computer Science, or related field

What will you need to be successful?

  • Minimum of 10 years experience across clinical data, AI/ML, and data platforms in medtech/pharma/biotech
  • Proven leadership of multi-domain teams (data management, engineering, data science, AI, programming)
  • Demonstrated ownership of enterprise data architecture (e.g., data lake/platform) - Databricks preferred
  • Strong track record supporting regulatory submissions and clinical evidence generation
  • Enterprise mindset - integrates data, AI, and operations into a unified capability
  • Technical depth + breadth - credible across data engineering, CDM, AI, and analytics
  • Regulatory credibility - understands how data and AI decisions impact submissions
  • Execution rigor - delivers scalable, high-quality platforms and outputs
  • Transformational leadership - embeds AI into workflows, not as isolated innovation
  • Pragmatic innovation - advances capabilities while maintaining compliance and reliability

You Unlimited.

  • The anticipated base compensation range for this position is $165,250-$236,000USD annually. The actual base pay offered to the successful candidate will be based on multiple factors, including but not limited to job-related knowledge/skills, experience, and geographic location. Compensation decisions are dependent upon the facts and circumstances of each position and candidate. In addition to base pay, we offer competitive bonus and benefits, including medical, dental, and vision coverage, 401(k), tuition reimbursement, medical leave programs, parental leave, generous PTO, paid company holidays, 8 hours of volunteer time annually, and a variety of wellness offerings such as EAP.

  • Inclusion + Belonging: Committed to Welcoming, Celebrating and Thriving. Learn more about our Employee Inclusion Groups on our website https://www.smith-nephew.com/

  • Your Future: 401k Matching Program, 401k Plus Program, Discounted Stock Options, Tuition Reimbursement

  • Work/Life Balance: Flexible Personal/Vacation Time Off, Paid Holidays, Flex Holidays, Paid Community Service Day

  • Your Wellbeing: Medical, Dental, Vision, Health Savings Account (Employer Contribution of $500+ annually), Employee Assistance Program, Parental Leave, Fertility and Adoption Assistance Program

  • Flexibility: Hybrid Work Model (For most professional roles)

  • Training: Hands-On, Team-Customized, Mentorship

  • Extra Perks: Discounts on fitness clubs, travel and more!

Smith+Nephew provides equal employment opportunities to applicants and employees without regard to race, color, religion, sex, sexual orientation, gender identity, national origin, protected veteran status, or disability.

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