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Clinical Data Associate Jobs in Boston, MA (NOW HIRING)

ECOG-ACRIN MRF

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Clinical Data Associate

Boston, MA · On-site

$50K - $62K/yr

The Data Associate is responsible for the quality control of patient data on one or more studies, working with Clinical Research Associates at member institutions, physicians and statisticians ...

New

MapLight Therapeutics

Clinical Data Manager

Burlington, MA · On-site

$145K - $160K/yr

Reporting to the Associate Director, the Clinical Data Manager, will play a pivotal role in ensuring the integrity, accuracy, and completeness of clinical trial data, contributing to the successful ...

Novartis

Clinical Data Engineering Lead

Cambridge, MA · On-site

Novartis Biomedical Research is searching for a visionary Associate Director to lead Clinical Data Engineering within their Oncology Data Science team. In this pivotal role, you'll be responsible for ...

Novartis

Clinical Data Engineering Lead

Cambridge, MA

$176K - $327K/yr

Novartis Biomedical Research (NBR) is searching for a visionary Associate Director to lead Clinical Data Engineering within our Oncology Data Science (OncDS) team. In this pivotal role, you'll be at ...

Eight Sleep

Clinical Data Engineer

Boston, MA · On-site

$124K - $149K/yr

The Role We're looking for a Clinical Data Engineer who will own the end-to-end data pipelines for ... associates to any issues, work closely with ML/AI to ensure that incoming data are stored in ...

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All JobsClinical Data Associate JobsClinical Data Associate Jobs in Boston, MA

Clinical Data Associate information

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$15

$42

$94

How much do clinical data associate jobs pay per hour?

As of Aug 8, 2026, the average hourly pay for clinical data associate 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 clinical data associates when ensuring data quality during clinical trials?

Clinical Data Associates often encounter challenges such as identifying and resolving discrepancies in large datasets, maintaining strict compliance with regulatory standards, and coordinating timely data entry from multiple sites. They must work closely with clinical research teams and data managers to clarify ambiguous data and implement data cleaning procedures. Staying organized and detail-oriented is essential to ensure data accuracy and the successful progression of clinical trials.

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

To thrive as a Clinical Data Associate, you need a solid understanding of clinical research, data management principles, and attention to detail, often supported by a degree in life sciences or a related field. Familiarity with clinical data management systems (CDMS), electronic data capture (EDC) tools, and knowledge of regulatory guidelines like GCP or CDISC is typically required. Strong organizational skills, analytical thinking, and clear communication set outstanding candidates apart in this role. These skills ensure the accuracy, integrity, and compliance of clinical trial data, which are crucial for successful research outcomes and regulatory approval.

What does a clinical data associate do?

A Clinical Data Associate is responsible for collecting, validating, and managing clinical trial data to ensure its accuracy, completeness, and compliance with regulatory standards. They work closely with clinical research teams to monitor data quality, resolve discrepancies, and prepare data for analysis. Their work is essential in supporting drug development and regulatory submissions by ensuring reliable and high-quality clinical data.

What does a clinical data associate do?

A clinical data associate is responsible for tracking data and results in a research study. As a clinical data associate, your job duties are to collect data, perform data management, and input data into any software used by your team. You work on a research team, so you must be able to work collaboratively and have excellent organizational skills. While you spend most of your time in an office, you may be required to work in the field to record data. The only universal qualifications needed for this career are a background in health care or medical science research and experience with data management software like Oracle Clinical, Microsoft Excel, and SPSS.

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

AspectClinical Data AssociateClinical Research Coordinator
Primary RoleManage and ensure accuracy of clinical trial dataOversee trial operations, patient recruitment, and site management
CredentialsBachelor's in life sciences or related field; familiarity with data managementBachelor's in health sciences or related field; clinical trial experience
Work EnvironmentData management teams, clinical trial databasesClinical sites, hospitals, research facilities
Industry UsagePharmaceutical companies, CROs, biotech firmsHospitals, research institutions, clinical trial sites

While both roles support clinical trials, a Clinical Data Associate primarily focuses on managing and validating trial data, ensuring accuracy and compliance. In contrast, a Clinical Research Coordinator handles the overall trial operations, including patient recruitment and site coordination. Both roles require relevant certifications and work within the clinical research industry, but their daily responsibilities differ significantly.

More about Clinical Data Associate jobs
What are the most commonly searched types of Clinical Data jobs in Boston, MA? The most popular types of Clinical Data jobs in Boston, MA are:
What are popular job titles related to Clinical Data Associate jobs in Boston, MA? For Clinical Data Associate jobs in Boston, MA, the most frequently searched job titles are:
What job categories do people searching Clinical Data Associate jobs in Boston, MA look for? The top searched job categories for Clinical Data Associate jobs in Boston, MA are:
What cities near Boston, MA are hiring for Clinical Data Associate jobs? Cities near Boston, MA with the most Clinical Data Associate job openings:
Clinical Data Associate jobs near you
Infographic showing various Clinical Data Associate job openings in Boston, MA as of August 2026, with employment types broken down into 67% Full Time, and 33% Contract. Highlights an 100% In-person job distribution, with an average salary of $88,016 per year, or $42.3 per hour.

Clinical Data Associate

ECOG-ACRIN MRF

Boston, MA • On-site

$50K - $62K/yr

Full-time

Medical, Dental, Life, Retirement

Posted 2 days ago

New

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Job description

FANTASTIC IMMEDIATE OPPORTUNITY for ENTRY LEVEL & EXPERIENCED candidates

Preference given to candidates with prior clinical research experience

All positions currently hybrid, working 1-2 days/week out of our Boston office.

The Data Associate is responsible for the quality control of patient data on one or more studies, working with Clinical Research Associates at member institutions, physicians and statisticians throughout this process. Great job for someone looking to get back into the workforce.

Duties include:

  • Review and evaluation of clinical patient data utilizing the electronic data capture system Medidata Rave®.
  • Assisting with the creation and validation of electronic case report forms and edit checks for their assigned studies.
  • Using a study specific Data Management Plan, review site reported data elements, generate manual queries, resolve answered queries.
  • Perform serious adverse event reconciliation between Rave® and the National Cancer Institute's safety database.
  • Review treatment information, evaluate response to treatment, and ensure follow-up and survival data are accurately coded and updated in the database in a timely way.
  • Work with the Study Chair to perform final case review. Review and provide input for protocols in development.
  • Assist the study chair and statistician with the preparation of the database for analysis.
  • Other duties as assigned.

Qualifications:

  • Bachelor's degree; preferably in one of the Life Sciences. Medical or biological sciences background is helpful but not required.
  • 1+ yr of experience; Previous experience with clinical studies is desired
  • Excellent organizational and interpersonal skills
  • Proficiency in database and word processing skills, and MS Office
  • Excellent written and verbal communication skills
  • Strong customer service skills and an ability to interact cordially with others
  • Attention to detail
  • Knowledge/experience with electronic data submission a plus, but will fully train qualified candidates.

Ideal candidate will have 1+ yr experience with a clinical studies background

All Candidates must submit a cover letter expressing their interest to be considered as well as answering the questions posted.

Complete training is provided to qualified candidates. Full time, 40 hour position, Monday - Friday during normal business hours (8-4 or 9-5).

Company Description

The ECOG-ACRIN Medical Research Foundation (EAMRF) serves as the grantee organization for the ECOG-ACRIN Cancer Research Group (Group). As a unique nonprofit organization, the overarching mission is to improve and increase patient awareness as well as facilitate access and promote participation in adult oncology clinical trials. The EAMRF provides the necessary support for EA to coordinate the scientific, administrative, governance and membership activities of the Group.

The EAMRF provides the support required to conduct oncology clinical trials. All the trials conducted under the auspices of the Group benefit public health by improving the quality and standard of care of patients with cancer. In addition, the organization promotes collaboration across the scientific community and encourages engagement of patient advocacy at all levels.