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Remote Clinical Data Reviewer Jobs (NOW HIRING)

Clinical Data Governance Lead, location is Remote. The start date is ASAP for this contract ... reviews, approvals, and stewardship activities. • Partner with clinical researchers to understand ...

Clinical Data Governance Lead, location is Remote. The start date is ASAP for this contract ... reviews, approvals, and stewardship activities. • Partner with clinical researchers to understand ...

Defining, running, and reviewing edit checks and resolving discrepant data * Maintaining organized ... Other duties as assigned This role is remote. Candidates located in the following states: AZ, CT ...

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Remote Clinical Data Reviewer information

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

As of Jul 15, 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:
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.
Sr. Manager, Clinical Data Management

Sr. Manager, Clinical Data Management

Moderna Therapeutics

Cambridge, MA • Remote

$130K - $209K/yr

Full-time

Medical, PTO

Posted 15 days ago


Moderna rating

8.9

Company rating: 8.9 out of 10

Based on 9 frontline employees who took The Breakroom Quiz

7th of 74 rated pharmaceutical


Job description

The Role:

Moderna Services, Inc. seeks a Sr. Manager, Clinical Data Management for its Cambridge, Massachusetts location.

Here's What You'll Do:

  • Lead data management activities for in-house and outsourced studies.

  • Responsible for vendor oversight activities across global development programs.

  • Represent data management function in clinical cross-functional meetings, ensuring aligned expectations between the Contract Research Organization (CRO) and Moderna for all data related deliverables, especially in support of key decision points and regulatory submissions.

  • Ensure established milestones and deliverables are met with the highest degree of quality.

  • Partner with appropriate stakeholders and CRO partners to mitigate and resolve risks.

  • Provide input to functional governance with Moderna strategic suppliers.

  • Partner with appropriate stakeholders to resolve issues escalated from the vendor and/or cross-functional teams.

  • Lead and manage clinical trial data collection set-up, data review, and database lock for studies where data management activities are conducted within Moderna.

  • Work with other functions to complete set up of Electronic Data Capture (EDC) and study data collection tools such as Inter-response time (IRT), ePRO and eCOA.

  • Lead the creation and maintenance of study cross functional data review plan components, including edit checks (data validation plan), listing review checks, data integration specifications, data transfer specifications, external data reconciliation plans, coding guidelines, Serious Adverse Events (SAE) reconciliation guidelines, and database lock plans.

  • Lead data review, including query management, and activities required for interim and final database locks.

  • Ensure archival and inspection readiness of all Data Management Trial Master File (TMF) documents.

  • Ensure achievement of major data management deliverables and milestones in coordination with the Clinical Operations Clinical Development, Biostatistics & Programming, Biomarker Operations & Sample Management and Pharmacovigilance.

  • Plan and manage external Data Management budgets and timelines to ensure accuracy, understand trends in variances and support continuous improvement in forecasting.

  • Act as a process expert for operational and oversight models.

  • Maintain Standard Operating Procedures (SOPs), process maps and templates and timelines to support functions operational and oversight models.

  • May prepare metrics to support the function Key Performance Indicators (KPIs).

  • Represent function in external professional initiatives and organizations such as SCDM, CDISC, and DIA to identify industry best practice and increase the visibility of Moderna.

  • Lead functional Continuous Improvement initiatives, providing strategic direction and identifying key deliverables that meet timelines, budget, and are in alignment with requirements.

  • Work cross-functionally to ensure the quality of the data in each database and on time delivery, as well as quality of other data management deliverables.

  • Champion and adopt technology improvements and tools for use in clinical data management processes.

  • Ensure compliance with own Learning Curricula, corporate and GXP requirements.

Here's What You'll Bring to the Table:

Minimum requirements:

  • Requires a Bachelor's degree, or foreign equivalent, in Biotechnology, Biology, Biological Sciences, or related field and 8 years of progressive, post-baccalaureate experience as a Sr. Manager, Assistant Clinical Data Manager, Clinical Data Associate or related position supporting clinical data management for the pharmaceutical industry.

  • 7 years of experience must include:

    • Vendor Management;

    • Medidata RAVE, InForm, and Oracle Clinical EDC tools;

    • Clinical Data Management using Biomarker and External data;

    • Utilizing eTMF tools;

    • Study Database Lock processes including Final, Interim, Snapshots, DSUR submission, and Staggered Lock;

    • Study Initiation, CSR Review, and SAE Reporting;

    • J-Review, I-Review, and Clinbrowser; and

    • SDTM and CDISC datasets, Clinical Data Studio, SQL & SAS.

  • 100% telecommuting permitted from anywhere within the US.

The salary range for this role is $130,800 to $209,400. This range reflects the lowest to highest salary we, in good faith, believe we would pay for this role at the time of this posting. The minimum target pay for this particular position, based on its primary location, is $196,400 to $209,400. An individual's placement within the range will depend on several factors, including but not limited to specific competencies, relevant education, qualifications, certifications, experience, skills, performance, and business or organizational needs.

Apply at https://modernatx.wd1.myworkdayjobs.com/en-US/M_tx (Job ID: R19409) or email resume and cover letter to careers@modernatx.com with subject line: R19409.

Pay & Benefits

At Moderna, we believe that when you feel your best, you can do your best work. That's why our US benefits and global well-being resources are designed to support you-at work, at home, and everywhere in between.

  • Best-in-class healthcare coverage, plus voluntary benefit programs to support your unique needs

  • A holistic approach to well-being, with access to fitness, mindfulness, and mental health support

  • Family planning benefits, including fertility, adoption, and surrogacy support

  • Generous paid time off, including vacation, volunteer days, sabbatical, global recharge days, and a discretionary year-end shutdown

  • Savings and investment opportunities to help you plan for the future

  • Location-specific perks and extras

The successful candidate may be eligible for an annual discretionary bonus, other incentive compensation, or equity award, subject to company plan eligibility criteria and individual performance.

#dni


Pay & Benefits

At Moderna, we believe that when you feel your best, you can do your best work. That's why our benefits and well-being resources are designed to support you-at work, at home, and everywhere in between.

  • Competitive healthcare, plus voluntary benefit programs to support your unique needs
  • A holistic approach to well-being, with access to fitness, mindfulness, and mental health support
  • Family planning benefits, including fertility, adoption, and surrogacy support
  • Generous paid time off, including vacation, volunteer days, sabbatical, global recharge days, and a discretionary year-end shutdown
  • Savingsandinvestmentsto help you plan for the future
  • Location-specific perks and extras

The successful candidate may be eligible for an annual discretionary bonus, other incentive compensation, or equity award, subject to company plan eligibility criteria and individual performance.


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About Moderna

Sourced by ZipRecruiter

In just over a decade, Moderna has evolved from a research-focused company in the messenger RNA (mRNA) field to a leading enterprise with a diverse clinical portfolio of vaccines and therapeutics. With a strong intellectual property portfolio and state-of-the-art manufacturing capabilities, Moderna collaborates with global partners to advance groundbreaking science and achieve rapid scaling of production. Notably, Moderna's mRNA platform has enabled the development of therapies for various diseases, including infectious diseases, immuno-oncology, and cardiovascular conditions. Recognized as a top biopharmaceutical employer, Moderna fosters an inclusive and smoke-free work environment. The company is dedicated to equal employment opportunities and non-discrimination, ensuring that all employees and applicants are treated with respect and without bias based on factors like race, gender, religion, disability, or sexual orientation. Moderna is also committed to providing reasonable accommodations for individuals with disabilities, in accordance with applicable laws. To know more, visit www.modernatx.com.

Industry

Manufacturing

Company size

501 - 1,000 Employees

Headquarters location

Cambridge, MA, US

Year founded

2010

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