ZipRecruiter

Log In

1

Senior Clinical Data Associate Jobs in Boston, MA

ECOG-ACRIN MRF

Be Seen First

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 ...

Clinovo

Sr Clinical Data Manager

Waltham, MA · On-site

The Senior Clinical Data Manager will be responsible for the oversight, coordination, and execution of clinical data management activities across one or more clinical trials. This individual will ...

TriNetX, LLC

Senior Clinical Study Analyst

Cambridge, MA · On-site

$120 - $170/hr

... TITLE: Sr. Clinical Study Analyst LOCATION: Cambridge, MA (hybrid) OR U.S. remote This position ... We keep identifiable data where it belongs--inside more than 11,000+ clinical sites across 20 ...

trinetx1

Senior Clinical Study Analyst

Cambridge, MA · On-site

We keep identifiable data where it belongs--inside more than 11,000+ clinical sites across 20 ... The Sr. Clinical Study Analyst will need to draw upon their extensive expertise across the areas of ...

RadNet

Senior Clinical Studies Associate

Somerville, MA · On-site

$71K/yr

Responsibilities Job Summary The Senior Clinical Studies Associate supports the planning, execution ... Conduct routine clinical data reviews and support data quality activities. * Ensure timely filing ...

next page

Showing results 1-20

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

Senior Clinical Data Associate information

See Boston, MA salary details

$42.9K

$64K

$79.8K

How much do senior clinical data associate jobs pay per year?

As of Sep 5, 2026, the average yearly pay for senior clinical data associate in Boston, MA is $64,029.00, according to ZipRecruiter salary data. Most workers in this role earn between $50,000.00 and $73,300.00 per year, depending on experience, location, and employer.

What does a senior clinical data associate do?

A Senior Clinical Data Associate is responsible for managing and ensuring the accuracy, integrity, and quality of data collected during clinical trials. They oversee data collection processes, review case report forms, resolve data discrepancies, and ensure compliance with regulatory standards. In addition to performing data management tasks, Senior Clinical Data Associates often mentor junior staff, contribute to developing data management plans, and collaborate with clinical research teams to ensure successful trial outcomes.

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

To thrive as a Senior Clinical Data Associate, you need expertise in clinical data management, data cleaning, and knowledge of clinical trial processes, supported by a degree in life sciences or a related field. Familiarity with data management systems like Medidata Rave, EDC platforms, and certifications such as CCDM are commonly required. Attention to detail, strong analytical thinking, and effective communication skills help you excel in ensuring data accuracy and collaborating with cross-functional teams. These capabilities are crucial for maintaining data integrity, regulatory compliance, and the overall success of clinical research studies.

What are some common challenges senior clinical data associates face when managing large clinical trial datasets?

Senior Clinical Data Associates often manage complex datasets from multiple sites, which can lead to challenges such as ensuring data consistency across sources, resolving discrepancies, and maintaining data integrity under tight timelines. Additionally, they must stay up-to-date with evolving regulatory requirements and work closely with cross-functional teams, including biostatisticians, clinical operations, and data managers, to ensure accurate and timely data delivery. Effective communication, attention to detail, and adaptability are essential to overcome these challenges and ensure successful trial outcomes.

What are the most commonly searched types of Senior Clinical Data jobs in Boston, MA?

The most popular types of Senior Clinical Data jobs in Boston, MA are:

What cities near Boston, MA are hiring for Senior Clinical Data Associate jobs?

Cities near Boston, MA with the most Senior Clinical Data Associate job openings:

Senior Clinical Data Associate jobs near you
Infographic showing various Senior Clinical Data Associate job openings in Boston, MA as of August 2026, with employment types broken down into 100% Full Time. Highlights an 50% In-person, and 50% Remote job distribution, with an average salary of $64,029 per year, or $30.8 per hour.

Clinical Data Associate

ECOG-ACRIN MRF

Boston, MA • On-site

$50K - $62K/yr

Full-time

Medical, Dental, Life, Retirement

Posted 29 days ago

Be Seen First

After you apply to this job, you can share why you’re interested to jump to the top of the candidate list.

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.