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Remote Clinical Data Reviewer Jobs (NOW HIRING)

Welo Data

German Bilingual Lyric Reviewer

Charleston, WV · Remote

$17 - $18/hr

Welo Data is looking for a German Lyric Reviewer to help us train cutting-edge AI. This role is ... Remote work, available to residents in many countries including Germany, US, Spain and Remote.

Natera

Senior Clinical Scientist, ECD

$142K - $178K/yr

... data review, and cross-functional problem solving while contributing to broader clinical development discussions and strategy. Location: San Carlos, CA or Remote, USA (West Coast or Mountain time ...

Natera

Senior Clinical Scientist, ECD

OR · On-site +1

... data review, and cross-functional problem solving while contributing to broader clinical development discussions and strategy. Location: San Carlos, CA or Remote, USA (West Coast or Mountain time ...

Danaher

Senior Clinical Data Manager

Vista, CA · On-site +1

... review. The essential requirements of the job include: * Bachelor's or master's degree in science ... We recognize the benefits of flexible, remote working arrangements for eligible roles and are ...

Danaher

Senior Clinical Data Manager

New York, NY · On-site +1

... review. The essential requirements of the job include: * Bachelor's or master's degree in science ... We recognize the benefits of flexible, remote working arrangements for eligible roles and are ...

Intuitive

Clinical Data Manager

Sunnyvale, CA · On-site +1

Including query management and data listing review. • Manage post-go live issues and requests ... Good Clinical Practices, Clinical research, Clinical trial process and related regulatory ...

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How much do remote clinical data reviewer jobs pay per hour?

As of Jul 16, 2026, the average hourly pay for remote 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 Remote Clinical Data Reviewers?

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 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 are some common challenges faced by Remote Clinical Data Reviewers, and how can they be managed effectively?

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

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.
More about Remote Clinical Data Reviewer jobs
What cities are hiring for Remote Clinical Data Reviewer jobs? Cities with the most Remote 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 Remote Clinical Data Reviewer jobs? States with the most job openings for Remote Clinical Data Reviewer jobs include:
What job categories do people searching Remote Clinical Data Reviewer jobs look for? The top searched job categories for Remote Clinical Data Reviewer jobs are:
Remote Clinical Data Reviewer jobs near you
Infographic showing various Remote Clinical Data Reviewer job openings in the United States as of July 2026, with employment types broken down into 72% Full Time, 11% Part Time, and 17% Contract. Highlights an 100% Remote job distribution, with an average salary of $54,583 per year, or $26.2 per hour.
Specialist Clinical Data Management

Specialist Clinical Data Management

Hollister Incorporated

Libertyville, IL • Remote

Other

Medical, Dental, Vision, Life, Retirement, PTO

Posted yesterday

New

Abercrombie & Fitch rating

6.2

Company rating: 6.2 out of 10

Based on 154 frontline employees who took The Breakroom Quiz

49th of 104 rated fashion retailers

Job description

We Make Life More Rewarding and Dignified 

Location: Libertyville
Department: Clinical Affairs 

Summary

The Specialist, Clinical Data Management (CDM) is a leader in supporting clinical studies for Hollister Incorporated medical device products and services. The CDM leads all aspects of clinical data management from study planning to database lock including EDC design, data review/cleaning, query management, data reconciliation, and data transfer. The CDM regularly collaborates with Global Clinical Affairs (GCA) study team members (Clinical Project Management, Biostatistics, Clinical Operations, Clinical Scientist) and cross-functional departments to ensure high data quality. The position operates under minimal supervision and independently evaluates, selects, and applies data management practices to a variety of research projects.

Responsibilities

Design and Planning

  • Lead the development of data management sections of clinical protocol and corresponding Case Report Forms (CRFs).
  • Develop and maintain data management essential documentation for the Trial Master File including, but not limited to; Data Management Plan, study-specific monitoring guidelines, edit checks, and user access forms, ensuring compliance with regulatory requirements
  • Support each clinical study and project team by ensuring data management plans, questionnaire development, and data handling activities are aligned to support the study objectives.
  • Participate in study team meetings

EDC Administration

  • Design and program clinical study databases in EDC System including but not limited to CRFs, edit checks, data dictionaries, queries/alerts, and managing user roles based on the clinical protocol
  • Lead User Acceptance Testing (UAT) to validate build specifications
  • Train clinical research personnel on the study-specific CRF, EDC/ePRO, and other project related items as needed.
  • Lead database clean, lock, export, and archiving activities.
  • Oversee data management vendor relationships including EDC partners and CROs supporting DM tasks
  • Continuously assess and enhance the EDC systems to improve efficiency and data quality

Data Monitoring

  • Monitor clinical data to resolve queries and data discrepancies throughout each study according to Clinical Protocol and/or Data Management Plan
  • Coordinates AE/DD reconciliation with PI
  • Identify and communicate data issues and/or query trends to study team and/or management.
  • Assist with developing metrics on study progress and routinely report out to study team and management.

Compliance and Process

  • Ensure data management activities comply with Good Clinical Practice (GCP), regulatory requirements, and internal standard operating procedures.
  • Contribute to the maintenance of GCA's data management procedures and work instructions
  • Responsible for leading or collaborating on process improvement initiatives within department
  • Meet study timelines with a high degree of quality
  • Other duties as needed or required. 
Essential Functions of the Role
  • Communicate effectively via email, phone, and virtual platforms.
  • Prepare reports and dashboards for internal stakeholders.
  • Ensure data accuracy and confidentiality in compliance with company and legal standards.
  • Manage multiple priorities and deadlines in a fast-paced environment.
  • Demonstrate initiative in identifying process improvements or automation opportunities.
  • Serve as a point of contact for internal and external stakeholders.
  • Resolve inquiries and issues with professionalism and discretion.
  • Adhere to company policies, including those related to ADA, data privacy, and ethics.
  • Maintain secure handling of sensitive information.
Education & Work Requirements
  • Bachelor's Degree with 2-5 years of related experience
Education & Work Preferences
  • Minimum of 2 years EDC database programming and Data Monitoring experience
  • Minimum of 2 years medical device and/or pharmaceutical clinical research experience
  • Certified Clinical Data Manager (CCDM) via SCDM or similar preferred
  • Equivalent combination of education, training and work experience may be accepted in lieu of degree.
  • Experience with EDC Systems (e.g. Medrio, Clinpal, Medidata Rave, etc.) required
  • Understanding of clinical research regulations required
  • Experience in questionnaire development, database structure, and data management processes
  • Experience with Microsoft Suite Applications (Word, PowerPoint, Excel, Teams)
  • Knowledge relating to continence care, critical care and/or ostomy a plus
Competencies
  • Be Agile - Innovates and adapts quickly, approaching change with curiosity while persisting through obstacles.
  • Be Customer Centric - Considers the needs, experiences and feedback of customers in all we do.
  • Be People-Focused - Builds trust and collaborates with an inclusive and empathetic approach.
  • Be Performance Driven - Operates with an ownership mindset, driving meaningful outcomes.
  • Live The Schneiders' Legacy, Our Noble Purpose - Passionately serves Our Mission and Vision, while demonstrating the Immutable Principles.

Benefits Statement

Our Total Rewards package in aggregate is above market and includes competitive pay, paid time off programs, peer-to-peer recognition, health and life insurance, wellness programs and incentives, and generous retirement savings.

  • The anticipated base pay range for this position is $77,000 - $120,000 yearly. The actual salary varies based on applicant's location, education, experience, skills, abilities, and other legitimate business factors.
  • If applicable: This position is also eligible to participate in the Hollister Secure Start Bonus Plan.
  • The Company's health and welfare benefits include medical, prescription, dental, vision, spending/savings accounts, disability, company paid (parental and caregiver) leaves, statutory leaves/disability programs, accident, life, wellbeing, education assistance, adoption assistance, and voluntary benefit programs. 
  • The Company's 401(k) Retirement Savings Plan includes: auto-enrollment, ROTH, vesting and eligible participants "safe harbor" matching contributions. 
  • The Company's paid time off benefits include: 11 paid holidays, paid vacation based on length of service and exempt/non-exempt status, and sick days based on statutory requirements and/or exempt/non-exempt status. 
  • The Company's additional benefits include: education assistance and adoption assistance benefit programs. 

About Hollister Incorporated
Hollister Incorporated is an independent, employee-owned company that develops, manufactures and markets healthcare products worldwide. The company spearheads the advancement of innovative products for ostomy care, continence care and critical care, and also creates educational support materials for patients and healthcare professionals. Headquartered in Libertyville, Illinois, Hollister has manufacturing and distribution centers on three continents and sells in nearly 80 countries. Hollister is a wholly owned subsidiary of The Firm of John Dickinson Schneider, Inc., and is guided both by its Mission to make life more rewarding and dignified for people who use our products and services, as well as its Vision to grow and prosper as an independent, employee-owned company, and in the process, to become better human beings.

EOE Statement
All qualified applicants will receive consideration for employment without regard to race, color, religion, sex, sexual orientation, gender identity, national origin, disability or protected veteran status.

Job Req ID: 36304

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