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Remote Cdisc Jobs (NOW HIRING)

MM International

Data Scientist

New York, NY · Remote

Remote Duration 4-6 months The RBQM Data Scientist supports central monitoring and risk-based ... CDISC, CDASH, SDTM standards. • Exposure to R, Python, or JavaScript and/or clinical data ...

BryceTech

Regulatory Data Technical Advisor

Washington, DC · On-site +1

$131.40K - $131.90K/yr

Ability to prioritize workload in a hybrid/remote work environment Preferred Qualifications: * Extensive knowledge of FDA/ICH guidelines and CDISC data standards preferred * Experience with applying ...

Hrcrs

Clinical Data Manager

El Paso, TX · Remote

Ensure adherence to CDISC/CDASH/SDTM standards , enabling efficient regulatory submission. Conduct ... This is a fully remote position and may be performed anywhere within the United States of America.

BryceTech

Regulatory Data Technical Advisor

Washington, DC · Remote

$131.40K - $131.90K/yr

Ability to prioritize workload in a hybrid/remote work environment Preferred Qualifications: * Extensive knowledge of FDA/ICH guidelines and CDISC data standards preferred * Experience with applying ...

BryceTech

Regulatory Data Technical Advisor

Washington, DC · Remote

$131.40K - $131.90K/yr

Ability to prioritize workload in a hybrid/remote work environment Preferred Qualifications: * Extensive knowledge of FDA/ICH guidelines and CDISC data standards preferred * Experience with applying ...

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$55

$84

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How much do remote cdisc jobs pay per hour?

As of Jun 4, 2026, the average hourly pay for remote cdisc in the United States is $84.56, according to ZipRecruiter salary data. Most workers in this role earn between $72.84 and $97.60 per hour, depending on experience, location, and employer.

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

To excel as a Remote CDISC Specialist, you need expertise in clinical data management, a thorough understanding of CDISC standards (such as SDTM and ADaM), and a relevant degree in life sciences or a related field. Proficiency with tools like SAS, Pinnacle 21, and clinical trial management systems, along with CDISC certification, is highly valued. Strong attention to detail, effective communication, and problem-solving abilities are crucial soft skills for this remote role. These competencies ensure accurate, compliant clinical data submissions and effective collaboration across distributed teams in regulatory environments.

What are some common challenges faced when working remotely as a CDISC specialist, and how can they be addressed?

As a remote CDISC specialist, one of the most common challenges is maintaining clear communication with clinical data teams and stakeholders across different time zones. Ensuring data standards compliance and timely submissions can also be complex without face-to-face collaboration. To address these challenges, it's important to set regular video meetings, use collaborative project management tools, and document processes clearly. Building strong virtual relationships and proactively seeking feedback can help ensure data integrity and project alignment.

What is a Remote CDISC professional?

A Remote CDISC professional is someone who works remotely to implement and manage data standards set by the Clinical Data Interchange Standards Consortium (CDISC) in clinical research. Their role typically involves converting, validating, and submitting clinical trial data to regulatory authorities in accordance with CDISC models, such as SDTM and ADaM. Remote CDISC professionals often collaborate with data managers, statisticians, and programmers to ensure data quality and compliance, utilizing specialized software and tools. Working remotely allows them to perform these tasks from any location, provided they have secure internet access and the necessary technical setup.

What is the difference between Remote Cdisc vs Remote Data Analyst?

AspectRemote CdiscRemote Data Analyst
Required CertificationsCDISC certifications, knowledge of CDISC standardsTypically a degree in data science, statistics, or related field; certifications vary
Work EnvironmentPharmaceutical/clinical research companies, CROs, remoteVarious industries including healthcare, finance, tech; remote options common
Industry UsagePrimarily in clinical research and pharmaceutical sectorsAcross multiple sectors including healthcare, finance, marketing
Common Search/ComparisonYesYes

Remote Cdisc specialists focus on clinical data standards and regulatory compliance within the pharmaceutical industry, often requiring CDISC certifications. Remote Data Analysts have broader roles across industries, analyzing data sets with varying tools and certifications. While both roles involve data handling, Remote Cdisc professionals specialize in clinical data standards, making their skills more industry-specific compared to the versatile role of Remote Data Analysts.

More about Remote Cdisc jobs
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Remote Cdisc jobs near you
Infographic showing various Remote Cdisc job openings in the United States as of May 2026, with employment types broken down into 76% Part Time, and 24% Contract. Highlights an 79% Physical, 2% Hybrid, and 19% Remote job distribution, with an average salary of $175,884 per year, or $84.6 per hour.
Clinical External Data Specialist

Clinical External Data Specialist

Redbock - an NES Fircroft company

Manhattan, NY • On-site, Remote

Full-time

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

Job description

A leading biotech organization based in the San Francisco Bay area is seeking an External Clinical Data Specialist for a remote 8+ month, renewable contract assignment. The External Data Acquisition Specialist (FSP) will support clinical trials by managing the acquisition, review, conformance, and quality control of external clinical data . This role focuses on ensuring that externally sourced data are delivered on time, meeting sponsor-defined standards, and conform to expected formats, structures, and specifications.

Key Responsibilities Manage end-to-end acquisition of external data sources (e.g., central labs, imaging, ePRO/eCOA, wearables, PK, biometrics, and other vendors) Perform external data conformance checks against sponsor-defined specifications, standards, and transfer agreements Review external data for completeness, structure, format, and consistency prior to integration or downstream use Identify, document, and escalate external data issues, discrepancies, and non-conformance findings Coordinate with vendors, data providers, and internal stakeholders to resolve external data conformance issues Maintain documentation related to external data transfers, conformance results, and issue resolution Support study milestones, interim data deliveries, and database lock activities related to external data Required Qualifications Bachelor's degree in Life Sciences, Health Sciences, Data Science, or related field Minimum 2 years of experience in Clinical Data Management with a focus on external data Hands-on experience managing external vendor data and data transfers Strong understanding of external data flow in clinical trials Experience performing data quality and conformance checks Knowledge of ICH-GCP, data standards, and regulatory expectations Preferred Qualifications Prior experience in an FSP or sponsor-dedicated model Familiarity with CDISC standards (SDTM concepts related to external data) Experience working with multiple external vendors and data types Strong issue-tracking and documentation skills High attention to detail and data quality focus Ability to work independently within sponsor-defined processes Strong communication and collaboration skills Proactive issue identification and resolution #J-18808-Ljbffr

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