ZipRecruiter

Log In

2

Full Time Edc Programmer Jobs in Boston, MA (NOW HIRING)

OpenClinica LLC

Customer Success Team Lead

Needham, MA · Remote

$12K/mo

Our industry-leading EHR-to-EDC connectivity automates source data acquisition, reduces errors, and ... S. * Status: Full-time, Exempt * Reports to: Vice President of Customer Success * Comp.: Base ...

All JobsEdc Programmer JobsFull Time Edc Programmer JobsFull Time Edc Programmer Jobs in Boston, MA

Full Time Edc Programmer information

See Boston, MA salary details

$13

$42

$74

How much do full time edc programmer jobs pay per hour?

As of Jul 30, 2026, the average hourly pay for full time edc programmer in Boston, MA is $42.95, according to ZipRecruiter salary data. Most workers in this role earn between $27.93 and $55.87 per hour, depending on experience, location, and employer.

What are the key skills and qualifications needed to thrive as a Full Time EDC Programmer, and why are they important?

To thrive as a Full Time EDC Programmer, you need strong programming skills (often in languages like SQL, Python, or SAS), a solid understanding of clinical data management, and typically a degree in computer science or a related field. Familiarity with Electronic Data Capture (EDC) systems such as Medidata Rave or Oracle InForm, and certifications in clinical data management or EDC platforms, are highly beneficial. Attention to detail, problem-solving abilities, and effective communication skills help ensure accurate data handling and collaboration with cross-functional teams. These skills are vital for ensuring high-quality clinical trial data, regulatory compliance, and the smooth operation of clinical research processes.

What is a Full Time EDC Programmer?

A Full Time EDC (Electronic Data Capture) Programmer is a professional who develops, configures, and maintains EDC systems used in clinical trials and research. Their main role is to design electronic case report forms (eCRFs), manage study databases, and ensure accurate data collection and validation. EDC Programmers collaborate closely with clinical teams, data managers, and statisticians to facilitate efficient and compliant data management. Working full time, they focus on supporting multiple studies, troubleshooting issues, and implementing new features or updates to the EDC system.

What are some common challenges faced by Full Time EDC Programmers during clinical trial projects?

Full Time EDC Programmers often encounter challenges such as integrating complex protocol requirements into electronic data capture (EDC) systems, ensuring data quality and regulatory compliance, and managing tight timelines. Collaboration is key, as programmers frequently work with data managers, clinical teams, and statisticians to address evolving data collection needs and troubleshoot technical issues. Staying up-to-date with evolving EDC software and regulatory standards is essential to effectively support clinical trial operations and ensure smooth data flow.

What is the difference between Full Time Edc Programmer vs Full Time Automation Engineer?

AspectFull Time Edc ProgrammerFull Time Automation Engineer
CredentialsProgramming certifications, technical degreesEngineering degrees, certifications in automation tools
Work EnvironmentElectronics manufacturing, R&D labsIndustrial plants, manufacturing facilities
Industry UsageElectronics, medical devices, aerospaceManufacturing, process industries

Full Time Edc Programmers focus on developing and maintaining embedded control systems for electronic devices, often working in electronics manufacturing environments. Automation Engineers design and implement automated processes in industrial settings. While both roles require technical programming skills and industry knowledge, Edc Programmers specialize in embedded systems, whereas Automation Engineers focus on process automation. The choice depends on your interest in embedded electronics versus industrial automation.

Full Time Edc Programmer jobs near you
Infographic showing various Full Time Edc Programmer job openings in Boston, MA as of June 2026, with employment types broken down into 1% As Needed, 86% Full Time, 11% Part Time, and 2% Contract. Highlights an 86% Physical, 2% Hybrid, and 12% Remote job distribution, with an average salary of $89,340 per year, or $43 per hour.

Manager Clinical Data

Monte Rosa Therapeutics, Inc

Boston, MA

Full-time

Re-posted 19 days ago

Job description

Overview

The Manager, Data Management will be responsible for overseeing clinical data management activities across one or more clinical programs. This individual will work closely with Clinical Operations, Biostats and  Programming, Medical, Safety, Regulatory, external CROs, and technology vendors to ensure high-quality, inspection-ready clinical data.

This is a hands-on role well suited for someone who thrives in a small biotech environment, can manage external partners effectively, and is comfortable moving between strategy, execution, and problem-solving.

Responsibilities
  • Oversee end-to-end clinical data management activities for assigned studies, from study start-up through database lock.
  • Manage CROs, EDC vendors, central labs, imaging vendors, eCOA providers, IRT vendors, and other data providers.
  • Review and contribute to key study documents, including data management plans, edit check specifications, CRF completion guidelines, data transfer agreements, and data review plans.
  • Support CRF design, database build, user acceptance testing, and EDC system validation activities.
  • Ensure timely data cleaning, query management, reconciliation, coding, and database lock activities.
  • Coordinate external data transfers and reconciliations, including laboratory, pharmacokinetic, biomarker, imaging, safety, and IRT data.
  • Partner with Clinical Operations and study teams to identify data quality issues and drive resolution.
  • Support medical coding activities using MedDRA and WHODrug, as applicable.
  • Contribute to clinical data review meetings and help prepare data outputs for internal decision-making.
  • Maintain data management documentation in compliance with GCP, ICH guidelines, SOPs, and regulatory expectations.
  • Support vendor selection, budget review, timelines, performance oversight, and issue escalation.
  • Contribute to process development and continuous improvement as the company scales its clinical operations infrastructure.
Qualifications
  • BS/MS degree in life sciences, data sciences, health sciences, or a related field.
  • 8+ years of clinical data management experience in biotech, pharmaceutical, CRO, or related clinical research settings.
  • Experience supporting oncology and/or immune disease clinical trials.
  • Strong working knowledge of EDC systems such as Medidata Rave or similar platforms.
  • Experience managing CROs and external clinical data vendors.
  • Familiarity with clinical trial data standards, including CDISC, SDTM concepts, and database lock processes.
  • Understanding of GCP, ICH guidelines, regulatory requirements, and clinical trial documentation standards.
  • Strong attention to detail, organizational skills, and ability to manage multiple priorities in a fast-paced environment.
  • Excellent communication and cross-functional collaboration skills.
  • Experience in a small biotech or emerging pharmaceutical company.
  • Experience with early-phase oncology trials, dose escalation, expansion cohorts, and complex biomarker-driven studies.
  • Familiarity with molecularly targeted therapies, protein degradation, or immune-mediated disease programs.
  • Experience with external data types such as genomics, biomarkers, PK/PD, central imaging, and specialty labs.
Employment Type: FULL_TIME

Apply