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Clinical Data Jobs in Boston, MA (NOW HIRING)

MapLight Therapeutics

Clinical Data Manager

Burlington, MA · On-site

$145K - $160K/yr

We are seeking a highly skilled and motivated Clinical Data Manager to join our Clinical Data Management team. Reporting to the Associate Director, the Clinical Data Manager, will play a pivotal role ...

Novartis

Clinical Data Engineering Lead

Cambridge, MA

$176.40K - $327.60K/yr

Define and implement the clinical data engineering roadmap in alignment with Novartis' data and digital strategy, collaborating with SMEs and OncDS leadership. * Integrate advanced tools and AI/ML ...

TScan Therapeutics

Clinical Data Manager

Waltham, MA

$130K - $150K/yr

Reporting to our Senior Clinical Data Manager the ideal candidate should have relevant experience in leading internal and external data management activities in oncology clinical studies and enjoy ...

TScan Therapeutics

Clinical Data Manager

Waltham, MA · On-site

$130K - $150K/yr

Reporting to our Senior Clinical Data Manager the ideal candidate should have relevant experience in leading internal and external data management activities in oncology clinical studies and enjoy ...

TScan Therapeutics

Clinical Data Manager

Waltham, MA

$130K - $150K/yr

Reporting to our Senior Clinical Data Manager the ideal candidate should have relevant experience in leading internal and external data management activities in oncology clinical studies and enjoy ...

Iterative Health

Clinical Data Manager

Cambridge, MA

$97K - $120K/yr

Clinical Research sector experience preferred * Familiarity with reading and understanding clinical research manuscripts and protocols * Familiarity with reviewing electronic health record data

Iterative Health

Clinical Data Manager

Cambridge, MA · On-site

$97K - $120K/yr

Clinical Research sector experience preferred * Familiarity with reading and understanding clinical research manuscripts and protocols * Familiarity with reviewing electronic health record data

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How much do clinical data jobs pay per hour?

As of May 28, 2026, the average hourly pay for clinical data in Boston, MA is $62.10, according to ZipRecruiter salary data. Most workers in this role earn between $49.09 and $73.89 per hour, depending on experience, location, and employer.

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

To thrive as a Clinical Data Specialist, you need a solid background in life sciences, data management principles, and familiarity with regulatory guidelines, often supported by a relevant degree. Proficiency in clinical data management systems (CDMS), electronic data capture (EDC) tools, and knowledge of standards like CDISC or MedDRA is typically required. Strong attention to detail, analytical thinking, and effective communication skills are crucial soft skills for this role. These competencies ensure the accuracy and integrity of clinical trial data, supporting regulatory compliance and reliable outcomes in clinical research.

What are some of the common challenges faced by professionals working in Clinical Data roles, and how can they be addressed?

Professionals in Clinical Data roles often encounter challenges such as managing large volumes of complex data, ensuring data quality and integrity, and adhering to strict regulatory standards. These challenges can be addressed by staying updated on industry best practices, utilizing advanced data management tools, and working closely with cross-functional teams such as clinical research and regulatory affairs. Continuous professional development and effective communication within the team are also key to overcoming these hurdles and ensuring successful clinical trial outcomes.

What are clinical data?

Clinical data refers to information collected during the course of ongoing patient care or as part of a clinical trial program. This data includes patient demographics, medical history, lab results, imaging studies, treatment plans, and outcomes. Clinical data is crucial for informing medical decisions, improving patient care, and supporting medical research and drug development. It is typically collected and managed by healthcare providers, researchers, and data professionals while maintaining strict standards for patient privacy and data security.

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

AspectClinical DataClinical Data Coordinator
CredentialsTypically requires a degree in health informatics, life sciences, or related fieldRequires similar credentials, often with additional certification in clinical research or data management
Work EnvironmentData analysis, database management, and reporting in healthcare or research settingsOversees data collection, entry, and quality control in clinical trial or healthcare environments
Employer & Industry UsageUsed across hospitals, research institutions, and pharmaceutical companiesCommonly employed in clinical research organizations and hospitals

While both roles involve handling clinical data, Clinical Data professionals focus on data analysis and management, whereas Clinical Data Coordinators oversee data collection and quality assurance in clinical trials or healthcare settings.

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 jobs in Boston, MA? For Clinical Data jobs in Boston, MA, the most frequently searched job titles are:
What job categories do people searching Clinical Data jobs in Boston, MA look for? The top searched job categories for Clinical Data jobs in Boston, MA are:
What cities near Boston, MA are hiring for Clinical Data jobs? Cities near Boston, MA with the most Clinical Data job openings:
Clinical Data jobs near you

Associate Director, Clinical Data

Clinical Dynamix

Waltham, MA • Hybrid

Full-time

This job post has expired today. Applications are no longer accepted.

Job description

ASSOCIATE DIRECTOR CLINICAL DATA MANAGEMENT (This role is based in Company's Waltham, MA headquarters. Their office-based employees follow a hybrid in-office schedule. 2 Days a week in office (3 days WFH)
Reporting to the Senior Director, Clinical Data Management, the Associate Director, Clinical Data Management will define and lead the clinical data management strategy for the organization. The Associate Director, Clinical Data Management is responsible for overseeing the start-up and execution of multiple, complex trials with a CRO and supporting upcoming submissions. The individual will coordinate and manage daily data management and vendor oversight activities for multiple clinical trials to support both the internal project team and the CROs.
Responsibilities (including, but not limited to):

  • Drive and lead the development of all databases and eCRF design
  • Plan, develop and implement UAT (user acceptance testing), data specifications, data entry guidelines, CRF completion guidelines, and related operational manuals/guidelines
  • Develop and execute data validation guidelines and measures to ensure accurate data gathering from clinical studies
  • Review and provide expertise on all eCRF changes, respond accordingly to make resulting database changes
  • Organize and direct the initial stage of the studies, review and sign off on various items such as eCRF, data validation, data review guidelines, and data management plans
  • Oversee and build strong sustainable relationships with multiple global CROs/vendors along with managing the process and coordination of each
  • Accountable for ensuring all data quality and timeliness of CDM deliverables are met and aligned with the business goals; Coordinate with all functions to drive data cleaning
  • Review, track, and report status of all data management project(s) to senior leadership
  • Responsible for managing the clinical trial data queries along with the planning and execution of medical coding and SAE reconciliation
  • Maintain data integrity in compliance with GCP, relevant SOPs and regulatory requirements by reviewing data processes and filing documentation in the trial master file (TMF)
  • Partner with cross functional key stake holders to meet project deliverables and timelines for clinical data acquisition, quality checking and reporting; Serve as internal expert on data management with vendors
  • Develop data management SOPs and processes that align and address business priorities; Contribute to cross-functional SOP development
  • Uphold a reputation for data integrity and compliance
Requirements
  • Requires a Bachelor's degree within a scientific discipline (advanced degree a plus) with a minimum of 10+ years of experience within biotech/biopharma and/or CRO organization
  • Extensive knowledge and experience in clinical data management
  • Direct experience with different Data Management systems and technologies, Electronic Data Capture systems and CDISC data standards
  • Extensive knowledge reviewing study planning documents such as Edit Check Specs, UAT scripts, Data Management Plans
  • Comprehensive understanding of database and dictionary structures (e.g., MedDRA, WHO DRUG)
  • Deep understanding of drug development, study conduct processes, GCP and regulations related clinical data management as well as ICH guidelines, FDA/EU regulations
  • Demonstrated experience in managing multiple CROs/vendors
  • Demonstrated strong written and verbal communication skills
  • Proven mindset of proactive continuous improvement
  • Efficient independent worker with ability to focus and drive for results
  • Strong attention to detail
  • Ability to work in a fast paced-environment and to handle multiple tasks
  • Strong commitment to ethical standards
  • Proficient with Microsoft Office suite (i.e., Word, PowerPoint, Excel, Outlook, SharePoint, etc.)
  • The salary range for this position is commensurate with experience

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