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Clinical Data Associate Remote Jobs (NOW HIRING)

Cytel

Principal Clinical Data Manager

Cambridge, MA · Remote

Principal Clinical Data Manager United States (Remote) Responsibilities - Responsible for vendor oversight activities across global development programs. - Represents data management function on the ...

Jj

Manager, Clinical Data Management

Horsham, PA · On-site +1

Clinical Data Management Job Category: Professional All Job Posting Locations: Horsham ... Remote work options may be considered on a case-by-case basis and if approved by the Company. About ...

Jj

Manager, Clinical Data Management

Titusville, NJ · On-site +1

Clinical Data Management Job Category: Professional All Job Posting Locations: Horsham ... Remote work options may be considered on a case-by-case basis and if approved by the Company. About ...

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How much do clinical data associate remote jobs pay per hour?

As of Aug 15, 2026, the average hourly pay for clinical data associate remote in the United States is $38.95, according to ZipRecruiter salary data. Most workers in this role earn between $29.33 and $38.94 per hour, depending on experience, location, and employer.

What are some common challenges faced by a clinical data associate working remotely, and how can they be managed?

Clinical Data Associates working remotely often face challenges related to communication and maintaining data quality standards across distributed teams. It can be more difficult to collaborate with clinical research coordinators, data managers, and other stakeholders without in-person interactions, making clear and timely communication essential. Utilizing secure data management platforms, participating in regular virtual meetings, and adhering strictly to data integrity protocols can help address these challenges. Proactively seeking feedback and staying updated on regulatory changes also contribute to maintaining high standards while working remotely.

What is a clinical data associate?

A Clinical Data Associate (Remote) is a professional who manages and verifies data collected during clinical trials, working from a remote location. They ensure the accuracy, integrity, and confidentiality of clinical trial data, collaborating with clinical teams and using specialized software. Their responsibilities include data entry, cleaning, validation, and generating reports to support regulatory submissions. Remote Clinical Data Associates utilize secure systems to access and manage data, allowing them to efficiently support clinical research from anywhere.

What are the key skills and qualifications needed to thrive as a clinical data associate?

To thrive as a Clinical Data Associate (Remote), you need a strong background in life sciences, data management, and an understanding of clinical trial processes, often supported by a relevant bachelor's degree. Familiarity with electronic data capture (EDC) systems, clinical data management software, and GCP (Good Clinical Practice) certification are commonly required. Attention to detail, problem-solving abilities, and effective virtual communication are crucial soft skills for managing data integrity and collaborating with remote teams. These skills and qualifications ensure the accurate collection, validation, and reporting of clinical trial data, which is essential for regulatory compliance and successful study outcomes.

What is the difference between Clinical Data Associate Remote vs Clinical Data Coordinator?

AspectClinical Data Associate RemoteClinical Data Coordinator
CredentialsBachelor's in life sciences or related field; familiarity with data management systemsBachelor's in health sciences or related field; experience with clinical data
Work EnvironmentRemote, primarily computer-basedTypically on-site or hybrid, working with clinical teams
Employer & IndustryPharmaceutical companies, CROs, biotech firmsHospitals, research institutions, clinical trial sites
Search & Comparison IntentYesYes

The Clinical Data Associate Remote and Clinical Data Coordinator roles share similarities in required education and industry usage. However, Clinical Data Associate Remote positions are primarily remote and focus on data entry and management from a distance, while Clinical Data Coordinators often work on-site, coordinating data collection and quality at clinical sites. Both roles are essential in clinical research but differ mainly in work setting and specific responsibilities.

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Clinical Data Associate Remote jobs near you
Infographic showing various Clinical Data Associate Remote job openings in the United States as of August 2026, with employment types broken down into 100% Full Time. Highlights an 100% Remote job distribution, with an average salary of $81,020 per year, or $39 per hour.

Principal Clinical Data Manager

Cytel

Cambridge, MA • Remote

Full-time

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

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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