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Senior Clinical Data Coordinator Jobs (NOW HIRING)

ProPharma Group

$80 - $100/hr

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 ...

Madrigalpharma

Clinical Data Coordinator

Conshohocken, PA · On-site

$80 - $100/hr

The Clinical Data Coordinator is responsible for supporting the collection, management, and quality assurance of clinical trial data to ensure data integrity and regulatory compliance. This role ...

Triwill Group

$125 - $150/hr

Our partner is looking for a Senior Clinical Data Manager based in United States. This role offers ... The position combines hands-on data oversight with study leadership, team coordination, and client ...

Clinovo

Sr Clinical Data Manager

Waltham, MA · On-site

The Senior Clinical Data Manager will be responsible for the oversight, coordination, and execution of clinical data management activities across one or more clinical trials. This individual will ...

City of Hope

Sr Clinical Trials Data Coord

Duarte, CA · On-site

The Senior Clinical Trials Data Coordinator supports complex oncology clinical trials from First-in-Human and Phase I through Phase IV by coordinating data collection, entry, quality assurance, and ...

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

As of Sep 7, 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 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 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.

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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, 85% Full Time, 11% Part Time, and 3% Contract. Highlights an 86% Physical, 3% Hybrid, and 11% Remote job distribution, with an average salary of $79,488 per year, or $38.2 per hour.

Senior Clinical Data Coordinator

Siro Clinpharm Pvt Ltd

Maple Grove, MN • On-site

Other

Posted 3 days ago

New

Job description

Job role: Senior Clinical Data Coordinator

Experience: 5 yrs

Location: Maple Grove, MN

Role Summary

The Senior Clinical Data Coordinator performs clinical data management activities across the study lifecycle to ensure the integrity, completeness, and quality of data in clinical databases and study files. Working under limited supervision, this role manages assigned studies, identifies and resolves data issues, supports study teams and sites, and helps improve clinical data management practices and procedures.

Key Responsibilities

• Supports testing and verification of clinical data management systems (CDMS).

• Manages data discrepancies by creating, routing, tracking, and resolving queries.

• Reviews clinical data forms, listings, and reports to identify inconsistencies and maintain database integrity.

• Supports reconciliation of data from multiple sources, including core laboratory and device data.

• Responds to site data needs, including support requests, patient transfers, and site closures.

• Performs data entry and quality control review for data received in paper or equivalent formats.

• Maintains accurate study metadata, including site, subject, and study personnel information.

• Provides administrative study support, including scanning, copying, redacting, filing, and related activities.

• Identifies root causes of data issues, facilitates resolution, and recommends preventive process improvements.

• Supports development and implementation of clinical data management practices, SOPs, and work instructions.

• Complies with FDA regulations, other applicable requirements, company policies, and operating procedures.

• Maintains effective, collaborative communication with employees, customers, contractors, vendors, and study partners.

Required Qualifications

• High school diploma or GED with specialized training or related experience, or an equivalent combination of education and work experience.

• Minimum 5 years of experience as a Clinical Data Coordinator or in a comparable clinical research environment with direct exposure to data management processes.

• Experience with clinical data management systems, such as Oracle Clinical.

• Strong organizational skills, attention to detail, and ability to perform recurring tasks with a high degree of accuracy.

• Ability to manage multiple studies, projects, priorities, and timelines under limited supervision.

• Strong written and verbal communication skills with the ability to work effectively across organizational levels.

• Ability to work independently and collaboratively in a fast-paced, changing environment while handling sensitive information with discretion.

• Proficiency with Microsoft Word, Excel, Outlook, Adobe, and related business applications.

• Ability to maintain regular attendance, work at a computer for extended periods, and support occasional overtime as required.

Preferred Qualifications

• Experience reconciling clinical data from core laboratories, medical devices, or other external data sources.

• Experience improving or implementing clinical data management practices, SOPs, or work instructions.

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