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Part Time Clinical Data Reviewer Jobs (NOW HIRING)

Grant Engine

This position is a part-time opportunity. Deliverables: · Review grants from various agencies and provide written feedback that follows the specific agency's format and criteria. · Provide detailed ...

The Pennsylvania State University

$21/hr

AND POSITION REQUIREMENTS EPCSE is seeking a Part Time Clinical Supervisor. The primary job ... Tasks include weekly individual supervision, review of intern paperwork, confirming and signing off ...

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Part Time Clinical Data Reviewer information

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How much do part time clinical data reviewer jobs pay per hour?

As of Jul 16, 2026, the average hourly pay for part time clinical data reviewer in the United States is $26.24, according to ZipRecruiter salary data. Most workers in this role earn between $14.42 and $36.30 per hour, depending on experience, location, and employer.

What are Part Time Clinical Data Reviewers?

Part Time Clinical Data Reviewers are professionals who work on a reduced or flexible schedule to review, validate, and ensure the accuracy of clinical trial data. They typically check data entries for completeness, consistency, and compliance with regulatory standards, helping to maintain the integrity of clinical research studies. Their work is essential in identifying discrepancies or errors in trial data before it is analyzed or submitted for regulatory approval. This role often requires attention to detail, familiarity with clinical data management systems, and knowledge of medical terminology.

What are some common challenges faced by part-time Clinical Data Reviewers, and how can they be addressed?

Part-time Clinical Data Reviewers often face challenges related to managing fluctuating workloads and maintaining effective communication with full-time team members. Since data review cycles may be intense and deadlines tight, staying organized and proactively coordinating availability with the team is crucial. Utilizing collaborative tools and participating in regular team meetings, even remotely, helps ensure alignment and timely issue resolution. Seeking clarity on project expectations and leveraging flexible work hours can help balance the part-time schedule with project demands.

What are the key skills and qualifications needed to thrive as a Part Time Clinical Data Reviewer, and why are they important?

To thrive as a Part Time Clinical Data Reviewer, you need a solid understanding of clinical research protocols, data management procedures, and typically a background in life sciences or a related field. Familiarity with electronic data capture (EDC) systems, clinical trial databases, and Good Clinical Practice (GCP) certification is often required. Excellent attention to detail, analytical thinking, and effective communication are important soft skills for this role. These skills ensure accurate data verification, regulatory compliance, and contribute to the reliability of clinical trial outcomes.

What is the difference between Part Time Clinical Data Reviewer vs Clinical Data Coordinator?

AspectPart Time Clinical Data ReviewerClinical Data Coordinator
CredentialsTypically requires a degree in life sciences or healthcare, with some roles preferring certification in clinical data managementSimilar credentials, often with additional project management or coordination experience
Work EnvironmentWorks in clinical research settings, reviewing data for accuracy and completenessCoordinates data collection, entry, and management across clinical trials
Employer & IndustryPharmaceutical companies, CROs, biotech firmsResearch organizations, hospitals, pharmaceutical companies
Search & Comparison IntentUnderstanding roles involving data review and quality controlFocus on data management and coordination tasks

The Part Time Clinical Data Reviewer primarily focuses on reviewing clinical trial data for accuracy, while the Clinical Data Coordinator manages data collection and entry processes. Both roles require similar educational backgrounds and work within the clinical research industry, but their responsibilities differ in scope and focus.

More about Part Time Clinical Data Reviewer jobs
What cities are hiring for Part Time Clinical Data Reviewer jobs? Cities with the most Part Time Clinical Data Reviewer job openings:
What are the most commonly searched types of Clinical Data Reviewer jobs? The most popular types of Clinical Data Reviewer jobs are:
What states have the most Part Time Clinical Data Reviewer jobs? States with the most job openings for Part Time Clinical Data Reviewer jobs include:
What job categories do people searching Part Time Clinical Data Reviewer jobs look for? The top searched job categories for Part Time Clinical Data Reviewer jobs are:
Part Time Clinical Data Reviewer jobs near you
Infographic showing various Part Time Clinical Data Reviewer job openings in the United States as of July 2026, with employment types broken down into 100% Part Time. Highlights an 100% In-person job distribution, with an average salary of $54,583 per year, or $26.2 per hour.
Clinical Trial Biostatistician

Clinical Trial Biostatistician

Cherokee Federal

Bethesda, MD • On-site

Part-time

Medical, Dental, Vision, Retirement

Re-posted 28 days ago

Job description


The Biostatistician will provide statistical and statistical-programming support for a Phase 2a randomized, double-blind clinical trial evaluating a hantavirus vaccine for the prevention of Hemorrhagic Fever with Renal Syndrome (WRAIR 2725). The Biostatistician will develop FDA-ready, CDISC-compliant deliverables, execute analyses per the approved Statistical Analysis Plan (SAP), and support generation of regulatory-submission outputs required for FDA filing and study close-out.
This is a fractional, deliverable-driven role with workload concentrated around dataset development, validation, and analysis milestones. Work supports Force Health Protection research and directly enables WRAIR's regulatory submission.
Compensation & Benefits:
Estimated Starting Salary Range: TBD
Pay commensurate with experience.
Full time benefits include Medical, Dental, Vision, 401K and other possible benefits as provided. Benefits are subject to change with or without notice.
Clinical Biostatistician Responsibilities Include:
Statistical Programming & Validation
  • Develop, program, and validate CDISC SDTM datasets from raw clinical data (e.g., demographics, adverse events, labs, vitals, concomitant medications).
  • Develop, program, and validate CDISC ADaM datasets to support planned analyses.
  • Maintain end-to-end traceability between raw data, SDTM, ADaM, and TLF outputs.
  • Perform independent QC and validation checks to ensure accuracy, completeness, and reproducibility.

Metadata & Submission Documentation
  • Create and maintain Define.XML for SDTM and ADaM deliverables.
  • Prepare the Study Data Reviewer's Guide (SDRG) for SDTM datasets.
  • Prepare the Analysis Data Reviewer's Guide (ADRG) for ADaM datasets.
  • Produce annotated CRFs mapping collection fields to SDTM variables and controlled terminology where applicable.

Statistical Analysis & Reporting
  • Review protocol, SAP, SOPs, and study-specific procedures; provide written notification of review and understanding.
  • Execute statistical analyses in full alignment with the approved SAP.
  • Produce Tables, Listings, and Figures (TLFs) and contribute statistical output and narrative content for the Final Clinical Study Report (FCSR) for regulatory submission.

Quality Assurance & Compliance
  • Ensure all deliverables meet current FDA CDISC standards and related guidance (including define/guide conventions and annotation expectations).
  • Produce documentation demonstrating CDISC compliance and audit readiness.
  • Meet performance expectations, including a 95% compliance standard against deliverable requirements, on-time submission, and minimal need for substantive revision.

Project Coordination & Communication
  • Coordinate with WRAIR CTC staff on data transfers, review cycles, and issue resolution.
  • Provide routine status updates on progress, risks, and dependencies; support inputs to the Program Management Plan (PMP) and Monthly Status Reports (MSRs).
  • Communicate effectively with Government leaders, scientists, and stakeholders; clearly identify contractor status in all interactions.

Indicative Deliverable Timeline (from study review start)
  • SDTM + ADaM datasets, Define.XML, SDRG, ADRG, annotated CRF: within 3 months
  • Statistical analyses completed: within 8 months
  • FCSR statistical deliverables completed: within 11 months

Clinical Biostatistician Experience, Education, Skills, Abilities requested:
Required Qualifications
  • Master's degree in Biostatistics, Statistics, or closely related quantitative field (or equivalent combination of education and experience).
  • Demonstrated experience producing CDISC-compliant SDTM and ADaM datasets and associated metadata/documents.
  • Strong statistical programming skills for clinical trials; SAS strongly preferred.
  • Working knowledge of FDA submission expectations for study data standards and documentation (Define.XML, SDRG/ADRG, CRF annotation).
  • Knowledge of GCP, ICH guidelines, and applicable 21 CFR requirements (including Parts 11, 50, 56, and 312).
  • Proficiency with Microsoft Office (Outlook, Word, PowerPoint, Excel) and Adobe PDF tools.
  • Strong written and verbal communication skills; able to operate effectively with Government stakeholders and cross-functional study teams.
  • Ability to work independently, manage shifting priorities, and deliver high-quality work on schedule in a deadline-driven environment.

Preferred Qualifications
  • PhD in Biostatistics or Statistics.
  • Experience supporting vaccine, infectious disease, and/or Phase 2 clinical trials.
  • Prior experience preparing statistical content for FDA regulatory submissions and clinical study reports.
  • Familiarity with DoD/military medical research environments and terminology.

Minimum Security Level:
  • Favorable Tier 1 NACI (or equivalent/higher) completed prior to start, or an open/pending investigation with no unfavorable information, as allowed by the customer.
  • Ability to obtain and maintain a Common Access Card (CAC) for on-site facility and network access.
  • Must be able to complete a National Agency Check and obtain installation access at WRAIR.
  • Mut pass pre-employment requirements of Cherokee Federal.

Company Information:
Cherokee Nation Integrated Health (CNIH) is a part of Cherokee Federal - the division of tribally owned federal contracting companies owned by Cherokee Nation Businesses. As a trusted partner for more than 60 federal clients, Cherokee Federal LLCs are focused on building a brighter future, solving complex challenges, and serving the government's mission with compassion and heart. To learn more about CNIH, visit cherokee-federal.com.
#CherokeeFederal #LI
Cherokee Federal is a military friendly employer. Veterans and active military transitioning to civilian status are encouraged to apply.
Legal Disclaimer: Cherokee Federal is an equal opportunity employer. Please visit cherokee-federal.com/careers for information regarding our Affirmative Action and Equal Opportunity Employer Statement, and Accommodation request.
Many of our job openings require access to government buildings or military installations. Candidates must pass pre-employment qualifications of Cherokee Federal.
Please Note:This position is pending a contract award.If you are interested in a future with Cherokee Federal, APPLY TODAY!Although this is not an approved position, we are accepting applications for this future and anticipated need.
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About Cherokee Federal

Sourced by ZipRecruiter

Cherokee Federal - a division of Cherokee Nation Businesses - is a team of tribally owned federal contracting companies focused on building solutions, solving complex challenges, and serving the nation's mission around the globe for more than 60 federal clients. Our team of companies manages nearly 1,000 projects of all sizes across the construction, consulting, engineering and manufacturing, health, and technology portfolios. Since 2012, the Cherokee Federal team of companies has won more than $5 billion in government contracts. Our 3,000+ employees work in 26 countries, 50 states and 2 U.S. territories. Why choose Cherokee Federal? Visit our website and learn about the great reasons to join our team. cherokee-federal.com

Industry

Architectural services

Company size

1,001 - 5,000 Employees

Headquarters location

Tulsa, OK, US

Year founded

1969

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