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Edc Jobs in Boston, MA (NOW HIRING)

TScan Therapeutics

Clinical Scientist

Waltham, MA

Support UAT testing of EDC systems and associated clinical technologies. * Review data transfer specifications and external vendor data integration processes. * Ensure data review activities align ...

TScan Therapeutics

Clinical Scientist

Waltham, MA · On-site

Support UAT testing of EDC systems and associated clinical technologies. * Review data transfer specifications and external vendor data integration processes. * Ensure data review activities align ...

TScan Therapeutics

Clinical Scientist

Waltham, MA

Support UAT testing of EDC systems and associated clinical technologies. * Review data transfer specifications and external vendor data integration processes. * Ensure data review activities align ...

Winaxis

Clinical Research Coordinator

Boston, MA · On-site

$26.25 - $35/hr

Collect, document, and maintain accurate study data in Case Report Forms (CRFs) and Electronic Data Capture (EDC) systems. Maintain essential regulatory documents, investigator site files, and study ...

Winaxis

Clinical Research Coordinator

Boston, MA · On-site

$26.25 - $35/hr

Collect, document, and maintain accurate study data in Case Report Forms (CRFs) and Electronic Data Capture (EDC) systems. Maintain essential regulatory documents, investigator site files, and study ...

Winaxis

Clinical Research Coordinator

Boston, MA · On-site

$26.25 - $35/hr

Collect, document, and maintain accurate study data in Case Report Forms (CRFs) and Electronic Data Capture (EDC) systems. Maintain essential regulatory documents, investigator site files, and study ...

Winaxis

Clinical Research Coordinator

Boston, MA · On-site

$26.25 - $35/hr

Collect, document, and maintain accurate study data in Case Report Forms (CRFs) and Electronic Data Capture (EDC) systems. Maintain essential regulatory documents, investigator site files, and study ...

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How much do edc jobs pay per hour?

As of Sep 1, 2026, the average hourly pay for edc in Boston, MA is $27.39, according to ZipRecruiter salary data. Most workers in this role earn between $22.26 and $31.44 per hour, depending on experience, location, and employer.

What is an EDC?

EDC stands for 'Everyday Carry.' In the context of jobs, an EDC typically refers to the essential tools, gadgets, or items that someone carries daily to be prepared for work or emergencies. This can include multitools, flashlights, pocket knives, pens, and other items tailored to the individual's profession or needs. People in security, law enforcement, medical fields, or even office environments often have different EDC items. The concept emphasizes practicality, preparedness, and efficiency in daily tasks.

What are the key skills and qualifications needed to thrive as an EDC specialist?

To thrive as an EDC Specialist, you need a solid understanding of clinical data management, data integrity principles, and experience with electronic data capture in clinical trials, often supported by a degree in life sciences or related fields. Familiarity with EDC systems like Medidata Rave or Oracle InForm, and certifications such as CDISC or GCP, are typically required. Attention to detail, problem-solving, and strong communication skills help you effectively collaborate with clinical teams and ensure high-quality data collection. These skills are crucial for accurate, compliant data management, which underpins the success of clinical research projects.

What are some common challenges faced by EDC professionals in clinical research, and how can they be managed?

Professionals working with Electronic Data Capture (EDC) systems in clinical research often encounter challenges such as ensuring data accuracy, maintaining regulatory compliance, and managing system updates. These challenges can be managed by staying up-to-date with industry regulations, participating in ongoing training, and collaborating closely with clinical teams to streamline data entry processes. Regular communication with IT and data management teams is also crucial to address technical issues promptly and ensure smooth workflows.

What are popular job titles related to Edc jobs in Boston, MA?

For Edc jobs in Boston, MA, the most frequently searched job titles are:

What job categories do people searching Edc jobs in Boston, MA look for?

The top searched job categories for Edc jobs in Boston, MA are:

What cities near Boston, MA are hiring for Edc jobs?

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Edc jobs near you
Infographic showing various Edc job openings in Boston, MA as of August 2026, with employment types broken down into 86% Full Time, 10% Part Time, and 4% Contract. Highlights an 78% Physical, 3% Hybrid, and 19% Remote job distribution, with an average salary of $56,795 per year, or $27.3 per hour.

Senior Manager, Global Clinical Affairs Data (Hybrid - Acton, MA)

Acton, MA • Hybrid

Insulet Corporation
Medical Equipment and Supplies Manufacturing • 501 - 1,000 employees
Learn more about Insulet Corporationexternal

$147K - $220K/yr

Full-time

Medical, Dental, Vision, Retirement, PTO

Re-posted 18 days ago

Job description

Job Summary

The Senior Clinical Data Manager is responsible for leading all aspects of the clinical data management lifecycle across multiple pre- and post-market studies, ensuring data integrity, regulatory compliance, and high-quality study execution. This role oversees EDC database design and validation, CRF development, data review, query management, database lock activities, and study closeout, while collaborating closely with cross-functional clinical teams. The position also drives process improvements, develops study metrics and tracking tools, supports investigator training, and serves as a subject matter expert on clinical data management best practices. The ideal candidate brings 6+ years of clinical data management experience, strong knowledge of GCP, FDA, HIPAA, GDPR, ISO, and 21 CFR Part 11 requirements, proficiency with multiple EDC platforms, and the ability to independently manage multiple priorities in a fast-paced environment.

Position Overview:

The Senior Clinical Data Manager is skilled in clinical data and systems management with demonstrated capability in coordinating activities across multiple studies. The Senior Clinical Data Manager contributes to process improvements and initiatives within the department and participates in all aspects of the clinical data management lifecycle.

Responsibilities:

  • Understand the device data collected as part of clinical studies (pre and post market) and manage the data ensuring compliance with protocol, regulatory, GDPR and HIPAA
  • Create and/or review study-specific Case Report Forms (CRFs) using prior device knowledge and protocol specific information. Work efficiently to incorporate clinical team input.
  • As applicable, develop Case Report Form Library of common forms that can be used consistently across studies.
  • Develop, build, and configure EDC databases.
  • Coordinate the validation and User Acceptance Testing (UAT) of EDC databases.
  • Develop and/or Review study-specific data management and database documentation, which may include Data Management Plan (DMP), CRF Completion Guidelines (CCGs), Annotated CRFs, Edit/Logic Check Specifications, and UAT Plans.
  • Collaborate with clinical team members to generate data review guidelines and perform data review and query generation/closure.
  • Prepare data for scheduled snapshots/database locks.
  • Perform appropriate database maintenance and closure and archival activities upon study completion.
  • Provide data management expertise and support to clinical colleagues using data management best practices.
  • Develops and provides study tracking and metrics tools to improve monitoring of study progress and data quality.
  • Collaborate with clinical colleagues to train Investigators and Coordinators on the EDC system, and the CRF completion guidelines as needed.
  • Identify improvements related to Clinical processes. As applicable, participate in development of a new process or revision of an existing process.
  • Monitor and ensure compliance with company policies and procedures (e.g. federal/country and regulatory requirements).

Education and Experience

  • Bachelor's degree and/or an equivalent combination of education or experience
  • Minimum of 6+ years of clinical data and/or systems experience
  • Strong computer skills with a proficiency with MS Windows based applications
  • Working knowledge of FDA regulations, Good Clinical Practices (GCP), and current industry practices related to the conduct of clinical trials this includes applicable ISO regulations for any trials conducted globally

Preferred Skills and Competencies:

  • Able to prioritize workload, assign realistic completion dates, and complete assignments on schedule.
  • Excellent written and oral communications skills required.
  • Comfortable with multiple Electronic Data Capture (EDC) Systems
  • Working knowledge of Good Clinical Practices (GCP), ISO, FDA regulations including 21 CFR part 11, and current industry practices related to the conduct of clinical trials, developing databases and managing protected health information.
  • Strong organizational skills and attention to detail.
  • Ability to work independently and manage multiple tasks in a fast-paced, changing environment.

Travel Requirements:

  • This position requires some travel up to 5% of the time.

NOTE: This position is eligible for hybrid working arrangements and requires on-site work from an Insulet office. #LI-Hybrid

Additional Information:

Compensation & Benefits: For U.S.-based positions only, the annual base salary range for this role is $147,000.00 - $220,500.00 This position may also be eligible for incentive compensation. We offer a comprehensive benefits package, including: Medical, dental, and vision insurance 401(k) with company match Paid time off (PTO) And additional employee wellness programs Application Details: This job posting will remain open until the position is filled. To apply, please visit the Insulet Careers site and submit your application online. Actual pay depends on skills, experience, and education.

Insulet Corporation (NASDAQ: PODD), headquartered in Massachusetts, is an innovative medical device company dedicated to simplifying life for people with diabetes and other conditions through its Omnipod product platform. The Omnipod Insulin Management System provides a unique alternative to traditional insulin delivery methods. With its simple, wearable design, the tubeless disposable Pod provides up to three days of non-stop insulin delivery, without the need to see or handle a needle. Insulet's flagship innovation, the Omnipod 5 Automated Insulin Delivery System, integrates with a continuous glucose monitor to manage blood sugar with no multiple daily injections, zero fingersticks, and can be controlled by a compatible personal smartphone in the U.S. or by the Omnipod 5 Controller. Insulet also leverages the unique design of its Pod by tailoring its Omnipod technology platform for the delivery of non-insulin subcutaneous drugs across other therapeutic areas. For more information, please visit insulet.com and omnipod.com.
We are looking for highly motivated, performance-driven individuals to be a part of our expanding team. We do this by hiring amazing people guided by shared values who exceed customer expectations. Our continued success depends on it!

At Insulet Corporation all qualified applicants will receive consideration for employment without regard to race, color, religion, sex, sexual orientation, gender identity, national origin, disability, or status as a protected veteran.

(Know Your Rights)

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About Insulet

Sourced by ZipRecruiter

Industry

Medical equipment and supplies manufacturing

Company size

501 - 1,000 Employees

Headquarters location

Billerica, MA, US

Year founded

2000

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