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Clinical Trial Data Management Jobs (NOW HIRING)

Jobtailor

Clinical Trial Specialist

California, MO · On-site

Collaborate with the Clinical Research Manager during site activation. * Ensure timely site data entry and query resolution. * Ensure accuracy, validity, and completeness of trial-site data. * Ensure ...

Kymera Therapeutics

Clinical Trial Manager

Watertown, MA

$115K - $200K/yr

Collaborate with the data management team to ensure data integrity and timely database lock. * Review and analyze clinical trial data to identify trends and potential issues. * Ensure tracking and ...

Kymera Therapeutics

Clinical Trial Manager

Watertown, MA · On-site

$115K - $200K/yr

Collaborate with the data management team to ensure data integrity and timely database lock. * Review and analyze clinical trial data to identify trends and potential issues. * Ensure tracking and ...

Parexel

Global Clinical Trial Leader - FSP

Seeking Clinical Trial Leaders in the US with Oncology and/or Inflammation Experience The Clinical ... Statistics, Data Management, Study Physician, Medical Writing, Site Monitoring) * Verifies and ...

Parexel

Global Clinical Trial Leader - FSP

Seeking Clinical Trial Leaders in the US with Oncology and/or Inflammation Experience The Clinical ... Statistics, Data Management, Study Physician, Medical Writing, Site Monitoring) * Verifies and ...

Hrcrs

Monitor and validate clinical trial data for accuracy, consistency, and completeness. * Ensure compliance with data management and monitoring procedures, standards, and regulatory guidelines.

R3TEK

Clinical Data Analyst

Hillsborough, NJ · On-site

Participate in clinical trial data management process. Conduct data analysis, visualization and data modeling based on report design in clinical data models including ambulatory, laboratory ...

R3tek

Clinical Data Analyst

Hillsborough, NJ · On-site

Participate in clinical trial data management process. Conduct data analysis, visualization and data modeling based on report design in clinical data models including ambulatory, laboratory ...

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How much do clinical trial data management jobs pay per hour?

As of Sep 15, 2026, the average hourly pay for clinical trial data management in the United States is $62.52, according to ZipRecruiter salary data. Most workers in this role earn between $50.72 and $70.43 per hour, depending on experience, location, and employer.

What is clinical trial data management?

Clinical trial data management involves the process of collecting, cleaning, and managing data generated during clinical research studies. Professionals in this field ensure that data is accurate, complete, and securely stored, following regulatory and quality standards. Their work is essential to ensure the reliability of trial results and supports regulatory submissions for new drugs or treatments. Data management teams use specialized software and follow strict protocols to maintain data integrity throughout the trial lifecycle.

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

To thrive as a Clinical Trial Data Manager, you need a strong background in life sciences, data management, and clinical research, often supported by a relevant degree and experience in clinical trials. Proficiency with electronic data capture (EDC) systems, clinical data management software (such as Medidata or Oracle Clinical), and knowledge of regulatory standards like GCP are essential. Attention to detail, strong organizational skills, and effective communication are vital soft skills for ensuring data accuracy and seamless collaboration with study teams. These competencies are crucial for maintaining data integrity, regulatory compliance, and the overall success of clinical research projects.

What are some common challenges faced by professionals in clinical trial data management, and how can they be addressed?

One of the primary challenges in clinical trial data management is ensuring data accuracy and integrity while coordinating with multiple teams, such as clinical research associates, statisticians, and regulatory affairs. Handling large volumes of complex data from different sources and adhering to strict regulatory timelines can be demanding. To address these challenges, strong communication skills, attention to detail, and proficiency with electronic data capture (EDC) systems are vital. Additionally, staying current with regulatory requirements and best practices helps ensure smooth and compliant data management throughout the clinical trial lifecycle.

What is the difference between Clinical Trial Data Management vs Clinical Data Coordinator?

AspectClinical Trial Data ManagementClinical Data Coordinator
ResponsibilitiesDesigning data collection processes, managing databases, ensuring data quality and integrityCollecting, entering, and verifying clinical trial data, supporting data queries
Required SkillsData management, database software, attention to detailData entry, communication skills, familiarity with clinical data systems
Work EnvironmentData management teams, clinical research organizations, pharmaceutical companiesClinical sites, research teams, data management departments
CertificationsOften requires knowledge of data management standards (CDISC, SDTM)Typically requires basic data entry and clinical trial knowledge

While both roles involve handling clinical trial data, Clinical Trial Data Management focuses on designing and overseeing data systems and ensuring data quality, whereas Clinical Data Coordinators primarily handle data entry and verification at clinical sites. Both roles are essential in the clinical research process and often collaborate closely.

What does data management do in clinical trial data management?

In clinical trial data management, the role involves collecting, cleaning, validating, and maintaining trial data to ensure accuracy and compliance with regulatory standards. Data managers use specialized software like EDC systems to organize and monitor data quality throughout the study. Their work supports reliable analysis and decision-making in the clinical development process.
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Clinical Trial Data Management jobs near you
Infographic showing various Clinical Trial Data Management job openings in the United States as of August 2026, with employment types broken down into 1% As Needed, 84% Full Time, 13% Part Time, and 2% Contract. Highlights an 84% Physical, 3% Hybrid, and 13% Remote job distribution, with an average salary of $130,034 per year, or $62.5 per hour.

Clinical Trial Specialist

California, MO • On-site

Jobtailor
See more jobs at Jobtailorexternal

Other

Posted 8 days ago

Job description

  • Act as primary local company contact for assigned trial sites.
  • Lead executional aspects of sponsored clinical trials with appropriate oversight.
  • Participate in site feasibility and pre-trial site assessment visits.
  • Attend investigator meetings as needed.
  • Complete site initiation, start-up, monitoring, site management, and site/study close-out activities according to SOPs, work instructions, and policies.
  • Develop clinical trial documents such as monitoring plans and informed consent documents.
  • Implement analytical risk-based monitoring at the site level and ensure timely issue resolution.
  • Collaborate with and may oversee Clinical Research Associates.
  • Ensure site staff training and accurate, complete training records.
  • Collaborate with the Clinical Research Manager during site activation.
  • Ensure timely site data entry and query resolution.
  • Ensure accuracy, validity, and completeness of trial-site data.
  • Ensure Adverse Events, Serious Adverse Events, and Product Quality Complaints are reported and documented within required timelines.
  • Oversee ordering, tracking, and accountability of investigational devices and trial materials.
  • Maintain complete and timely trial data and essential documents in relevant systems.
  • Document trial activities, write visit reports and follow-up letters, and communicate status and issues.
  • Review study files and ensure archiving and retention requirements.
  • Attend team meetings and training and develop therapeutic knowledge.
  • Work with the Clinical Trial Leader on CAPA completion for QA audits and site quality issues.
  • Prepare sites for close-out and conduct final close-out visits.
  • Track site-level costs and ensure payments are made when applicable.
  • Maintain relationships with internal and external partners, investigators, trial coordinators, and site staff.
  • Contribute to process improvement and training.
  • Lead or participate in special initiatives and may serve as a Champion or Subject Matter Expert.
Requirements
  • A Bachelor Degree is required, preferably a Bachelor of Science Degree in Life Science, Physical Science, Nursing or Biological Science.
  • 3+ years of experience working in clinical trials is required; MS with at least 2 years, PhD with at least 1 year of related experience.
  • Previous clinical research experience is required.
  • Good understanding of clinical research science and processes, clinical trends, and global clinical trial regulations.
  • Previous experience in medical device monitoring is strongly preferred.
  • Understanding and application of regulations and standards applied in clinical research areas and medical devices/combination products.
  • Relevant industry certifications preferred (i.e., CCRA, RAC, CDE).
  • Ability and willingness for up to 40% travel, mostly domestic, is required.
  • Clinical/medical background preferred.
  • Experience and knowledge working with Microsoft Office: Excel, Word, PowerPoint and Outlook.
  • Strong computer skills in appropriate software and related company clinical systems.
  • Presentation and influencing skills.
  • Strong organizational skills, including managing multiple sub-projects and tasks and meeting deadlines.
Core Competencies

Demonstrates expertise in managing clinical trials, including site initiation, monitoring, and close-out activities, while ensuring compliance with regulations and standards. Proficient in developing clinical trial documents and maintaining accurate trial data and essential documents.

Highest-signal resume keywords
  • Clinical Trial Management
  • Site Monitoring
  • Regulatory Compliance
  • Clinical Research Experience
  • Data Management
Hard Skills
  • Clinical Trial Execution
  • Site Feasibility Assessment
  • Monitoring Plan Development
  • Risk-Based Monitoring
  • Adverse Event Reporting
  • Data Entry and Query Resolution
  • Investigational Device Accountability
  • CAPA Completion
  • Process Improvement
  • Therapeutic Knowledge
Soft Skills
  • Presentation Skills
  • Organizational Skills
  • Influencing Skills
Certifications & Qualifications
  • CCRA
  • RAC
  • CDE
Industry Keywords
  • Clinical Research
  • Medical Device Monitoring
  • Global Clinical Trial Regulations
  • Life Science
  • Biological Science
Tools & Technologies
  • Microsoft Office
  • Clinical Systems
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