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Clinical Data Associate Remote Jobs in Boston, MA

Clinical Data Analyst

Somerville, MA · On-site +1

$94 - $128/hr

Job Summary The Senior Clinical Data Analyst independently executes assigned clinical studies ... Travel This position requires domestic / international travel up to 10%. Working Environment Remote ...

Principal Clinical Data Manager United States (Remote) Responsibilities - Responsible for vendor oversight activities across global development programs. - Represents data management function on the ...

Lead data management for complex, global clinical trials from study setup to database lock. * Serve as the main client contact for all data management deliverables. * Oversee SAE, PK, and external ...

Lead data management for complex, global clinical trials from study setup to database lock. * Serve as the main client contact for all data management deliverables. * Oversee SAE, PK, and external ...

Title - Technical Lead - Data Analysis Location - Boston, MA - Remote JD - Key Skills * Advanced ... Deep expertise in claims and/or clinical data * Strong understanding of medical economics, risk ...

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Clinical Data Associate Remote information

See Boston, MA salary details

$15

$42

$94

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

As of Aug 5, 2026, the average hourly pay for clinical data associate remote in Boston, MA is $42.32, according to ZipRecruiter salary data. Most workers in this role earn between $31.88 and $42.31 per hour, depending on experience, location, and employer.

What are some common challenges faced by a clinical data associate working remotely, and how can they be managed?

Clinical Data Associates working remotely often face challenges related to communication and maintaining data quality standards across distributed teams. It can be more difficult to collaborate with clinical research coordinators, data managers, and other stakeholders without in-person interactions, making clear and timely communication essential. Utilizing secure data management platforms, participating in regular virtual meetings, and adhering strictly to data integrity protocols can help address these challenges. Proactively seeking feedback and staying updated on regulatory changes also contribute to maintaining high standards while working remotely.

What is a clinical data associate?

A Clinical Data Associate (Remote) is a professional who manages and verifies data collected during clinical trials, working from a remote location. They ensure the accuracy, integrity, and confidentiality of clinical trial data, collaborating with clinical teams and using specialized software. Their responsibilities include data entry, cleaning, validation, and generating reports to support regulatory submissions. Remote Clinical Data Associates utilize secure systems to access and manage data, allowing them to efficiently support clinical research from anywhere.

What are the key skills and qualifications needed to thrive as a clinical data associate?

To thrive as a Clinical Data Associate (Remote), you need a strong background in life sciences, data management, and an understanding of clinical trial processes, often supported by a relevant bachelor's degree. Familiarity with electronic data capture (EDC) systems, clinical data management software, and GCP (Good Clinical Practice) certification are commonly required. Attention to detail, problem-solving abilities, and effective virtual communication are crucial soft skills for managing data integrity and collaborating with remote teams. These skills and qualifications ensure the accurate collection, validation, and reporting of clinical trial data, which is essential for regulatory compliance and successful study outcomes.

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

AspectClinical Data Associate RemoteClinical Data Coordinator
CredentialsBachelor's in life sciences or related field; familiarity with data management systemsBachelor's in health sciences or related field; experience with clinical data
Work EnvironmentRemote, primarily computer-basedTypically on-site or hybrid, working with clinical teams
Employer & IndustryPharmaceutical companies, CROs, biotech firmsHospitals, research institutions, clinical trial sites
Search & Comparison IntentYesYes

The Clinical Data Associate Remote and Clinical Data Coordinator roles share similarities in required education and industry usage. However, Clinical Data Associate Remote positions are primarily remote and focus on data entry and management from a distance, while Clinical Data Coordinators often work on-site, coordinating data collection and quality at clinical sites. Both roles are essential in clinical research but differ mainly in work setting and specific responsibilities.

What job categories do people searching Clinical Data Associate Remote jobs in Boston, MA look for? The top searched job categories for Clinical Data Associate Remote jobs in Boston, MA are:
Infographic showing various Clinical Data Associate Remote job openings in Boston, MA as of June 2026, with employment types broken down into 1% As Needed, 72% Full Time, 24% Part Time, 2% Contract, and 1% Nights. Highlights an 90% Physical, 2% Hybrid, and 8% Remote job distribution, with an average salary of $88,020 per year, or $42.3 per hour.

Sr. Manager, Clinical Data Management

Moderna Therapeutics

Cambridge, MA • Remote

$130K - $209K/yr

Full-time

Medical, PTO

Re-posted 4 days ago


Moderna rating

9.2

Company rating: 9.2 out of 10

Based on 10 frontline employees who took The Breakroom Quiz

5th of 86 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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