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Senior Clinical Data Coordinator Jobs (NOW HIRING)

Actalent

Clinical Data Coordinator

New Haven, CT

$28 - $31.83/hr

Clinical Data Coordinator We are seeking a Clinical Data Coordinator to join the Clinical Trials Office at a renowned Cancer Center. This hybrid position involves working on-site for two days per ...

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Actalent

Clinical Data Coordinator

New Haven, CT

$28 - $31.83/hr

Clinical Data Coordinator๏ปฟ We are seeking a Clinical Data Coordinator to join the Clinical Trials Office at a renowned Cancer Center. This hybrid position involves working on-site for two days per ...

New

Ocugen Inc

Senior Clinical Data Manager

Malvern, PA ยท On-site

Position Summary The Senior Clinical Data Manager plays a pivotal role within Ocugen's clinical data management team. This individual will lead data management efforts, oversee quality data ...

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How much do senior clinical data coordinator jobs pay per hour?

As of Aug 15, 2026, the average hourly pay for senior clinical data coordinator in the United States is $38.22, according to ZipRecruiter salary data. Most workers in this role earn between $25.24 and $56.01 per hour, depending on experience, location, and employer.

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

To thrive as a Senior Clinical Data Coordinator, you need a strong background in clinical research, data management, and regulatory compliance, typically supported by a degree in life sciences or a related field. Proficiency with clinical data management systems (CDMS), electronic data capture (EDC) tools, and familiarity with industry standards like CDISC are essential. Attention to detail, strong organizational skills, and effective communication abilities help ensure data integrity and facilitate cross-functional teamwork. These competencies are crucial for maintaining high-quality clinical trial data, regulatory adherence, and smooth study operations.

How does a senior clinical data coordinator typically collaborate with other departments in a clinical trial setting?

A Senior Clinical Data Coordinator regularly works with cross-functional teams, including clinical research associates, data managers, biostatisticians, and project managers. Their role involves ensuring data integrity and accuracy by facilitating clear communication among these groups, addressing data queries, and resolving discrepancies. They may also participate in meetings to align on study timelines, review progress, and implement data management best practices, contributing to the overall success of clinical trials.

What is the difference between Senior Clinical Data Coordinator vs Clinical Data Coordinator?

AspectSenior Clinical Data CoordinatorClinical Data Coordinator
Required CredentialsBachelor's degree, experience in data management, possibly certificationBachelor's degree, entry-level experience in data management
Work EnvironmentClinical research settings, hospitals, pharmaceutical companiesClinical research sites, hospitals, CROs
Employer & Industry UsageUsed in larger organizations with complex trialsCommon in various research settings, often entry-level
Search & Comparison IntentUnderstanding advanced responsibilities and qualificationsEntry-level role, basic data management tasks

The main difference between a Senior Clinical Data Coordinator and a Clinical Data Coordinator lies in experience, responsibilities, and qualifications. Senior roles typically require more experience, advanced skills, and may involve overseeing data management processes. Both roles are essential in clinical research environments, but the senior position indicates a higher level of expertise and leadership within the data management team.

What does a senior clinical data coordinator do?

A Senior Clinical Data Coordinator is responsible for overseeing the collection, management, and quality control of clinical trial data. They ensure that the data collected from clinical studies is accurate, complete, and compliant with regulatory standards. Their tasks include designing data collection tools, monitoring data entry, resolving discrepancies, and liaising with clinical teams. Additionally, they often mentor junior coordinators and contribute to the development of data management plans and processes.

What are the most commonly searched types of Senior Clinical Data jobs?

The most popular types of Senior Clinical Data jobs are:

What states have the most Senior Clinical Data Coordinator jobs?

States with the most job openings for Senior Clinical Data Coordinator jobs include:

What are popular job titles related to Senior Clinical Data Coordinator jobs?

For Senior Clinical Data Coordinator jobs, the most frequently searched job titles are:

Senior Clinical Data Coordinator jobs near you
Infographic showing various Senior 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 $79,488 per year, or $38.2 per hour.

Sr. Clinical Data Coordinator

ProPharma Group

Charleston, WV โ€ข On-site, Remote

Full-time

Posted 3 days ago

New

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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