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Remote Edc Programmer Jobs in Bridgeport, CT (NOW HIRING)

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Remote Edc Programmer information

See Bridgeport, CT salary details

$12

$40

$69

How much do remote edc programmer jobs pay per hour?

As of Aug 1, 2026, the average hourly pay for remote edc programmer in Bridgeport, CT is $40.20, according to ZipRecruiter salary data. Most workers in this role earn between $26.15 and $52.31 per hour, depending on experience, location, and employer.

What is the difference between Remote Edc Programmer vs Remote Clinical Data Coordinator?

AspectRemote Edc ProgrammerRemote Clinical Data Coordinator
Required CredentialsTypically requires a degree in computer science, life sciences, or related field; proficiency in EDC systemsUsually requires a degree in health sciences, life sciences, or related; knowledge of clinical data management
Work EnvironmentPrimarily focused on programming and system setup within clinical trialsOversees data collection, entry, and quality control in clinical studies
Employer & Industry UsagePharmaceutical companies, CROs, biotech firmsPharmaceutical companies, CROs, research institutions

The Remote Edc Programmer primarily focuses on designing and programming electronic data capture systems for clinical trials, requiring technical programming skills. In contrast, the Remote Clinical Data Coordinator manages data collection and quality assurance processes. Both roles are essential in clinical research but differ in technical focus and daily responsibilities.

What is a Remote EDC Programmer?

A Remote EDC Programmer is a professional who designs, develops, and manages Electronic Data Capture (EDC) systems for clinical trials or research studies, working from a remote location. They are responsible for programming databases, building electronic case report forms (eCRFs), and ensuring that data collection processes meet regulatory and quality standards. EDC Programmers collaborate with clinical teams to customize systems according to study protocols and troubleshoot technical issues to ensure smooth data collection and management. Their remote role allows them to work with organizations and clients globally, leveraging secure communication and data tools.

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

To thrive as a Remote EDC (Electronic Data Capture) Programmer, you need a solid background in clinical data management, database design, and programming languages such as SQL, often supported by a degree in computer science or a related field. Familiarity with EDC systems like Medidata Rave, Oracle InForm, and knowledge of relevant regulatory standards (e.g., CDISC, FDA 21 CFR Part 11) are typically required. Strong problem-solving skills, attention to detail, and effective communication are essential soft skills for collaborating remotely with cross-functional clinical teams. These skills ensure accurate data capture, regulatory compliance, and efficient study execution in clinical trials.

What are some common challenges Remote EDC Programmers face when collaborating with cross-functional teams, and how can they overcome them?

Remote EDC Programmers often work closely with data managers, clinical trial coordinators, and statisticians, which can present challenges such as time zone differences, communication barriers, and varying technical expertise. Overcoming these challenges typically involves using clear documentation, regular virtual check-ins, and collaborative platforms to ensure alignment on project goals and timelines. Building strong relationships with team members and proactively addressing issues can also help ensure smooth collaboration and successful study database development.
What job categories do people searching Remote Edc Programmer jobs in Bridgeport, CT look for? The top searched job categories for Remote Edc Programmer jobs in Bridgeport, CT are:
Remote Edc Programmer jobs near you
Infographic showing various Remote Edc Programmer job openings in Bridgeport, CT as of June 2026, with employment types broken down into 81% Full Time, and 19% Contract. Highlights an 100% Remote job distribution, with an average salary of $83,613 per year, or $40.2 per hour.

Technical Clinical Data Manager /Data Analyst (Remote)

Penfield Search Partners

Fairfield, CT • Remote

Other

Posted yesterday

New

Job description

Job Description Contact: Neisha Camacho/Terra Parsons - teamnt@penfieldsearch.com No 3rd party candidates We are partnering with a growing biotech organization seeking a Clinical Data Manager/Data Analyst to support ongoing and upcoming clinical programs across multiple therapeutic areas. This role will sit within a highly collaborative clinical development team and is ideal for a hands-on, analytical Clinical Data Manager who enjoys digging into the data, identifying trends or issues proactively, and developing creative solutions to improve data quality and study execution. The client is seeking someone resourceful and technically curious - not just process-oriented - with the ability to independently explore datasets, generate meaningful reports, and surface potential issues early

The ideal candidate will bring a blend of traditional clinical data management expertise along with strong data review, querying, and analytical skills. Experience with R, SQL, SAS, or other data interrogation and reporting tools is highly desirable. Key Responsibilities Support clinical data management activities across studies from start-up through database lock Perform hands-on data review and exploratory analysis to identify data trends, inconsistencies, missing data patterns, and potential study risks Develop custom reports, listings, and data visualizations to support proactive data cleaning and study oversight Utilize R, SQL, SAS, or similar tools to query, analyze, and troubleshoot clinical datasets Partner with CROs and vendors to ensure high-quality, timely data delivery Collaborate cross-functionally with Clinical Operations, Biostatistics, Statistical Programming, Medical, and Safety teams on data review strategies and issue resolution Contribute to development and review of key deliverables including: Data Management Plans (DMPs) eCRF design and completion guidelines Edit checks and query logic User Acceptance Testing (UAT) Data review plans and cleaning processes Support ongoing query management and ensure data integrity, consistency, and inspection readiness Assist with implementation of data standards, reporting enhancements, and process improvements Work independently to investigate data anomalies and recommend practical solutions in a fast-paced biotech environment Qualifications BS in a scientific, technical, or clinical discipline Approximately 5-8 years of clinical data management experience within biotech, pharma, or CRO environments Strong hands-on experience reviewing and interrogating clinical trial data Experience using R, SQL, SAS, or other querying/reporting tools to analyze clinical data and generate custom reports Experience with EDC systems such as Medidata Rave, Oracle, or Veeva Working knowledge of CDISC standards (SDTM/ADaM) and downstream data usage Experience supporting Phase II and/or III clinical trials; CNS experience is a plus Exposure to CRO/vendor oversight Understanding of clinical data structures and dictionaries including MedDRA and WHODrug Strong critical thinking and problem-solving skills with the ability to work independently Resourceful, proactive, detail-oriented, and comfortable operating in a dynamic biotech environment Strong communication and cross-functional collaboration skills.

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