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Remote Cdisc Jobs (NOW HIRING)

Cytel

Principal Clinical Data Manager

Cambridge, MA · Remote

Principal Clinical Data Manager United States (Remote) Responsibilities - Responsible for vendor ... CDISC, DIA, etc. to identify industry best practice and increase the visibility of client ...

Cytel

Principal Statistical Programmer FSP

Extensive applied experience of CDISC standards (SDTM, ADaM, and Define.xml), medical terminology ... Locations Remote, London, London, WC2B 4HN, GB Remote, Abla, Andalucia, 04510, ES Cape Town, 8005 ...

New

Vrtx

Principal Statistical Programmer

Boston, MA · Remote

$149K - $223K/yr

Intermediate knowledge of CDISC Standards * Intermediate knowledge of clinical trials * Regulatory ... Remote-Eligible Flex Eligibility Status: In this Remote-Eligible role, you can choose to be ...

Celerion

EDC Developer / Programmer

OR · Remote

This is a full time, remote opportunity, but may travel for training and key meetings. As an EDC ... Maintain global clinical trial database standards (CDISC) Requirements: * Bachelor's degree in a ...

Celerion

EDC Developer / Programmer

This is a full time, remote opportunity, but may travel for training and key meetings. As an EDC ... Maintain global clinical trial database standards (CDISC) Requirements: * Bachelor's degree in a ...

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All JobsRemote Cdisc Jobs

Remote Cdisc information

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$55

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How much do remote cdisc jobs pay per hour?

As of Jun 25, 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 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.

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 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 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.
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Remote Cdisc jobs near you
Infographic showing various Remote Cdisc job openings in the United States as of June 2026, with employment types broken down into 91% Full Time, 6% Part Time, and 3% Contract. Highlights an 37% Physical, 3% Hybrid, and 60% Remote job distribution, with an average salary of $175,884 per year, or $84.6 per hour.
Principal Clinical Data Manager

Principal Clinical Data Manager

Cytel

Cambridge, MA • Remote

Full-time

Posted 8 days ago

Job description

Principal Clinical Data Manager United States (Remote) JOB DESCRIPTION Responsibilities - Responsible for vendor oversight activities across global development programs. - Represents data management function on the Clinical Sub-team ensuring aligned expectations between the CRO and client for all data related deliverables, especially in support of key decision points and regulatory submissions. - Contributes influential leadership in collaboration with other client Stakeholders to ensure established milestones and deliverables are met with the highest degree of quality.

- Partners with appropriate stakeholders and CRO partners to mitigate and resolve risks. - Provides input to functional governance with client strategic suppliers. Partners with appropriate stakeholders to resolve issues escalated from the vendor and/or cross-functional teams.

- Participates in preparing function for submission readiness and may represent function in a formal inspection or audit. - Participates and represents function in formal inspections and audits as requested. - Ensure archival and inspection readiness of all Data Management Trial Master File (TMF) documents.

Ensures achievement of major data management deliverables and milestones in coordination with other functions including the Therapeutic Area Units, Clinical Operations, Statistical Programming and Statistics. - Responsible for the planning and management of external Data Management budgets and timelines to ensure accuracy, understand trends in variances and support continuous improvement in forecasting. - Acts as a process expert for operational and oversight models.

- Maintains SOPs, process maps and templates and timelines to support functions operational and oversight models. - May prepare metrics to support the function’s KPIs. - Represents function in external professional initiatives and organizations such as SCDM, CDISC, DIA, etc.

to identify industry best practice and increase the visibility of client. - Contributes or Leads functional Continuous Improvement initiatives, providing strategic direction and identifying key deliverables that meet timelines, budget, and are in alignment with company, departmental or functional requirements. - Ensure compliance with own Learning Curricula, corporate and/or GXP requirements.

- Works cross-functionally to ensure the quality of the data in each database and on time delivery, as well as quality of other data management deliverables. - Performs other duties as assigned Qualifications Educational qualifications: - MS or BS in health-related, life sciences area or technology-related field. Minimum Work Requirements: - Minimum of 10 years data management and/or drug development process with expertise in the cross-functional interfaces with the data management function.

- Proven track record of strong project management skills and experience managing data management activities for large drug development programs. - Experience with all phases of development in one or more therapeutic areas preferred. - Ability to handle multiple development programs simultaneously.

- NDA/CTD Experience preferred. - Strong knowledge of data management best practices & technologies as applied to clinical trials. - Solid understanding of clinical trial documents (protocols, statistical analysis plans, CRFs, study reports) and processes.

- Expert knowledge of FDA and ICH regulations and industry standards applicable to data capture and data management process. - Advanced knowledge of broad drug development process with expertise in the cross-functional interfaces with the data management function. APPLY NOW JOB INFO Job Identification 1311 Job Category Clinical Data Insights & Analytics Posting Date 17/02/2026, 00:38 Locations Remote, Cambridge, MA, 02139, US (Remote)

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