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Edc Jobs in Boston, MA (NOW HIRING)

Adams Clinical

Clinical Research Assistant

Watertown, MA · On-site

$22 - $24/hr

Perform data entry into EDC systems and assist with query resolution. * Maintain study binders, charts, and logs; support supply management. * Ensure accurate capture and upload of paper source ...

Adams Clinical

Clinical Research Assistant

Boston, MA · On-site

$24 - $26.92/hr

Perform data entry into EDC systems and assist with query resolution. * Maintain study binders, charts, and logs; support supply management. * Ensure accurate capture and upload of paper source ...

Adams Clinical

Clinical Research Assistant

Boston, MA · On-site

$24 - $26.92/hr

Perform data entry into EDC systems and assist with query resolution. * Maintain study binders, charts, and logs; support supply management. * Ensure accurate capture and upload of paper source ...

Adams Clinical

Clinical Research Assistant

Boston, MA · On-site

$24 - $26.92/hr

Perform data entry into EDC systems and assist with query resolution. * Maintain study binders, charts, and logs; support supply management. * Ensure accurate capture and upload of paper source ...

Adams Clinical

Clinical Research Assistant

Boston, MA · On-site

$24 - $26.92/hr

Perform data entry into EDC systems and assist with query resolution. * Maintain study binders, charts, and logs; support supply management. * Ensure accurate capture and upload of paper source ...

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All JobsEdc JobsEdc Jobs in Boston, MA

Edc information

See Boston, MA salary details

$16

$27

$38

How much do edc jobs pay per hour?

As of Aug 10, 2026, the average hourly pay for edc in Boston, MA is $27.31, according to ZipRecruiter salary data. Most workers in this role earn between $22.21 and $31.35 per hour, depending on experience, location, and employer.

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 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 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 cities near Boston, MA are hiring for Edc jobs? Cities near Boston, MA with the most Edc job openings:
Edc jobs near you
Infographic showing various Edc job openings in Boston, MA as of August 2026, with employment types broken down into 88% Full Time, 6% Part Time, and 6% Contract. Highlights an 84% Physical, 4% Hybrid, and 12% Remote job distribution, with an average salary of $56,798 per year, or $27.3 per hour.

Associate Director, Clinical Data Management

Prime Medicine

Watertown, MA • On-site

Full-time

Medical, Dental, Vision, Life, Retirement, PTO

Re-posted 22 days ago

Job description

Company Overview:
Prime Medicine is a leading biotechnology company dedicated to creating and delivering the next generation of gene editing therapies to patients. The Company is leveraging its proprietary Prime Editing platform, a versatile, precise and efficient gene editing technology, to develop a new class of differentiated, one-time, potentially curative genetic therapies. Designed to make only the right edit at the right position within a gene while minimizing unwanted DNA modifications, Prime Editors have the potential to repair almost all types of genetic mutations and work in many different tissues, organs and cell types.
Prime Medicine is currently progressing a diversified portfolio of investigational therapeutic programs organized around our core areas of focus: hematology, immunology & oncology, liver and lung. Across each core area, Prime Medicine is focused initially on a set of high value programs, each targeting a disease with well-understood biology and a clearly defined clinical development and regulatory path, and each expected to provide the foundation for expansion into additional opportunities. For more information, please visit www.primemedicine.com.
Position Overview
Prime Medicine is seeking an experienced Associate Director of Clinical Data Management to lead clinical data strategy and execution across gene editing programs from first-in-human studies through regulatory submission. This role will oversee all internal and external data management activities supporting INDs, CTAs, BLAs, and global regulatory filings.
The ideal candidate has experience in rare disease clinical trials, vendor oversight, and complex biologic or gene therapy programs, and is comfortable operating in a fast-paced environment. This individual will ensure clinical data integrity, regulatory readiness, and high-quality execution across the development portfolio.
This role reports to the Senior Director, Clinical Operations.
Key Responsibilities
Clinical Data Leadership
  • Lead all clinical data management activities across multiple programs from IND through BLA submission.
  • Develop and execute data management strategies aligned with regulatory requirements both in the US/ex-US
  • Oversee CRF design, database build, edit checks, data review, coding, reconciliation, and database lock.
  • Ensure implementation of CDISC standards (SDTM/ADaM) to support submission readiness.
  • Support inspection readiness and maintain audit-ready documentation.

Vendor Oversight & Governance
  • Lead selection, oversight, and performance management of CRO and data management vendors.
  • Manage vendor budgets, timelines, KPIs, and quality metrics.
  • Oversee external data transfers and reconciliation processes (e.g., SAE, lab, PK and PD).
  • Ensure change control, database archiving, and data governance processes are compliant and well documented.

Gene Therapy & Rare Disease Expertise
  • Oversee integration of complex data streams including:
    • Genomic and sequencing data
    • Biomarker and translational endpoints
    • Immunogenicity and PK/PD
    • Long-term follow-up safety data
  • Support dose-escalation studies with rapid data review cycles and SRC/DMC readiness
  • Tailor data processes to rare disease trial realities (small populations, adaptive designs, multi-cohort studies).

Systems & Infrastructure
  • Contribute to scalable data infrastructure and identification of key efficiencies between programs
  • Support implementation and optimization of EDC, ePRO, IRT, and data visualization systems.
  • Ensure integration between clinical data, laboratory systems, and sample tracking systems.

Cross-Functional Collaboration
  • Partner with Clinical Development, Clinical Operations, Regulatory, Quality, and Translational Sciences.
  • Serve as subject matter expert for data standards, governance, and process improvement initiatives.
  • Contribute to development and improvement of internal SOPs and workflows.

Qualifications
  • Bachelor's degree in life sciences, statistics, informatics, or related field (advanced degree preferred).
  • 8+ years of progressive clinical data management experience, including leadership responsibility.
  • Experience supporting IND submissions and major regulatory filings (BLA/NDA/MAA).
  • Direct experience in rare disease and/or gene therapy, gene editing, or advanced biologics strongly preferred.
  • Demonstrated CRO/vendor oversight experience in global trials.
  • Strong knowledge of ICH/GCP, FDA/CFR regulations, CDISC standards, and eCTD submission requirements.
  • Experience with EDC systems, medical coding (MedDRA/WHO Drug), and external data integration.
  • Strong understanding of safety data reconciliation and regulatory inspection preparedness.
  • Excellent organizational, project management, and communication skills.

Key Competencies
  • Strategic thinker with strong execution skills.
  • Detail-oriented with high standards for data quality and compliance.
  • Collaborative and cross-functional mindset.
  • Comfortable working in a dynamic, innovative biotech environment.
  • Passion for advancing transformative therapies for patients with rare genetic diseases.

The pay range reflects the full-time base salary range we expect to pay for this role at the time of posting. Base pay will be determined based on several factors including, but not limited to, relevant experience, skills, and education. This role is eligible for an annual short-term incentive award (e.g., bonus) and an annual long-term incentive award (e.g., equity).
Prime Medicine offers a comprehensive Total Rewards package with robust health, financial, and wellness benefits-including medical, dental, vision, life insurance, a 401(k) match, and equity programs-along with generous paid time off, wellness days, and company-wide recharge breaks.
Our commitment to employee well-being reflects our belief that when we care for our people, we strengthen our ability to put patients first and make meaningful impact together.
U.S. Pay Range
$174,000-$193,000 USD
Prime Medicine is proud to be an equal opportunity employer. All qualified applicants will receive consideration for employment without regard to race, color, religion, sex, national origin, age, sexual orientation, gender identity, disability, veteran status, or any other classification protected by law.

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