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Intern Remote Clinical Data Coordinator Jobs (NOW HIRING)

ProPharma Group

Clinical Data Manager

Charleston, WV · On-site +1

Responsible for providing data review training and guidance to Sr. Clinical Data Coordinators that ... Whilst ProPharma supports remote working, we also recognise the value that comes from in person ...

New

CSAA Insurance Group, a AAA Insurer

$32/hr

Job Title 2027 Actuarial Intern - Remote Requisition Number R7874 2027 Actuarial Intern - Remote ... Compiles data, performs statistical analysis, and summarizes results * Work on a capstone project ...

DivIHN

Business Analytics- Intern (Remote)

Charlotte, NC · On-site +1

Title: Business Analytics- Intern (Remote) Duration: 9 Months Location: Charlotte, NC Prefered ... Use data-driven approaches, statistical modeling, and machine learning tools to extract insights ...

New

Faeth Therapeutics

Clinical Data Manager

Austin, TX · Remote

$175K/yr

Remote (U.S.) Responsibilities: * Lead day-to-day data management activities for assigned clinical trials (Phase 2 and Phase 1b) * Oversee CRO and vendor data management deliverables to ensure ...

Faeth Therapeutics

Clinical Data Manager

Austin, TX · Remote

$125K - $175K/yr

Remote (U.S.) Responsibilities: * Lead day-to-day data management activities for assigned clinical trials (Phase 2 and Phase 1b) * Oversee CRO and vendor data management deliverables to ensure ...

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How much do intern remote clinical data coordinator jobs pay per hour?

As of Aug 17, 2026, the average hourly pay for intern remote clinical data coordinator in the United States is $17.04, according to ZipRecruiter salary data. Most workers in this role earn between $14.42 and $19.23 per hour, depending on experience, location, and employer.

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

AspectIntern Remote Clinical Data CoordinatorIntern Remote Clinical Research Associate
CredentialsBasic coursework in life sciences, data managementRelated coursework, some certifications in clinical research
Work EnvironmentRemote, data-focused tasks in clinical settingsRemote, monitoring and site visits in clinical trials
Industry UsageData management in healthcare and pharmaMonitoring and oversight in clinical trials

The Intern Remote Clinical Data Coordinator primarily handles data entry, management, and analysis remotely, focusing on maintaining accurate clinical data. In contrast, the Intern Remote Clinical Research Associate involves monitoring clinical trial sites and ensuring compliance remotely. Both roles require related certifications and are used in similar industry settings, but they differ in daily responsibilities and focus areas.

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Intern Remote Clinical Data Coordinator jobs near you
Infographic showing various Intern Remote Clinical Data Coordinator job openings in the United States as of August 2026, with employment types broken down into 1% As Needed, 84% Full Time, 11% Part Time, and 4% Contract. Highlights an 86% Physical, 4% Hybrid, and 10% Remote job distribution, with an average salary of $35,436 per year, or $17 per hour.

Sr. Clinical Data Coordinator

ProPharma Group

Charleston, WV • On-site, Remote

Full-time

Posted 5 days ago

Job description

For the past 25 years, ProPharma has improved the health and wellness of patients by providing advice and expertise that empowers biotech, med device, and pharmaceutical organizations of all sizes to confidently advance scientific breakthroughs and introduce new therapies. ProPharma partners with its clients through an advise-build-operate model across the complete product lifecycle.With deep domain expertise in regulatory sciences, clinical research solutions, quality & compliance, pharmacovigilance, medical information, and R&D technology, ProPharma offers an end-to-end suite of fully customizable consulting solutions that de-risk and accelerate our partners' most high-profile drug and device programs.

Title: Senior Clinical Data Coordinator

FSP/Contractor

Job Summary

The Sr. Clinical Data Coordinator performs activities pertaining to the conduct of Phase I-IlI clinical trials in accordance with ICH/Good Clinical Practices (GCP) and other relevant procedures and guidelines to ensure that a quality work product is produced and timelines and deliverables are met.

Summary of the Essential Functions of the Job

  • Perform ongoing data review, including reconciliation of third party data streams and serious adverse event reconciliation with the safety database.
  • Perform User Acceptance Testing (UAT) of clinical databases.
  • Perform Quality Control (QC) of clinical databases.
  • Perform ongoing updates of Data Management-related documentation, as needed.

Minimum Requirements

  • Bachelor's degree OR certification in a related allied health profession from an appropriately accredited institution (i.e. RN, MT, PA, RT) is preferred, but individuals with commensurate experience will be considered.
  • Minimum of 3 years of data management experience is required.
  • Experience with Electronic Data Capture (EDC) system(s) is required.
  • Experience with Oracle Inc.'s Inform EDC system is preferred.
  • Oncology and/or inflammatory therapeutic area experience is preferred.

#LI-REMOTE

#LI-AP1

We celebrate our differences and strive to create a workplace where each person can be their authentic self. We are committed to diversity, equity, and inclusion. Employees are encouraged to unleash their innovative, collaborative, and entrepreneurial spirits. With a holistic approach as an Equal Opportunity Employer, we provide a safe space where all employees feel empowered to succeed.

All applications to roles at ProPharma are personally reviewed by a member of our recruitment team. We do not rely on AI screening tools to support our hiring process. You will always receive an outcome to your application so that you have an answer from us - whether you're successful or not.

Whilst ProPharma supports remote working, we also recognise the value that comes from in person collaboration. As such, we encourage any new hires that are based within a reasonably short commute of one of our offices to work on a hybrid basis and spend some time working from that office location, as agreed with your manager. All applications will be treated on their own merit and candidates will not be at any advantage or disadvantage based on their proximity to an office.

***ProPharma Group does not accept unsolicited resumes from recruiters/third parties. Please, no phone calls or emails to anyone regarding this posting.***

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