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Clinical Data Management Internship information

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

As of Jun 10, 2026, the average hourly pay for clinical data management internship in the United States is $16.59, according to ZipRecruiter salary data. Most workers in this role earn between $15.38 and $20.19 per hour, depending on experience, location, and employer.

What is a Clinical Data Management Internship?

A Clinical Data Management Internship is a temporary position designed for students or recent graduates to gain hands-on experience in collecting, managing, and analyzing data from clinical research trials. Interns work under the supervision of experienced data managers and help ensure that clinical trial data is accurate, complete, and securely maintained. Tasks often include data entry, quality control, database maintenance, and assisting with regulatory compliance. This internship provides valuable exposure to the processes and standards required in clinical research, preparing individuals for a career in clinical data management.

What types of projects and tasks can I expect to work on during a Clinical Data Management Internship?

During a Clinical Data Management Internship, you’ll typically assist with tasks such as data entry, validation, and cleaning of clinical trial data, as well as supporting database setup and quality control reviews. Interns often work closely with data managers and clinical research associates to ensure data integrity and compliance with regulatory standards. You may also be involved in preparing reports, learning to use industry-standard data management software, and participating in team meetings to discuss project progress. This provides a valuable introduction to the workflow of clinical trials and offers insight into how data supports critical decision-making in drug development.

What are the key skills and qualifications needed to thrive as a Clinical Data Management Intern, and why are they important?

To thrive as a Clinical Data Management Intern, you need a background in life sciences or a related field, strong attention to detail, and an understanding of clinical research processes. Familiarity with data management systems like Oracle Clinical or Medidata Rave, and knowledge of regulatory requirements such as GCP, are often expected. Strong analytical thinking, effective communication, and teamwork skills will help you excel in collaborating with cross-functional teams and ensuring data integrity. These skills are crucial for maintaining high-quality clinical trial data and supporting successful regulatory submissions.

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

AspectClinical Data Management InternshipClinical Data Coordinator
Required CredentialsTypically students or recent graduates, some knowledge of clinical data systemsBachelor's degree in life sciences, healthcare, or related field; experience preferred
Work EnvironmentInternship setting, often in pharmaceutical or biotech companiesFull-time role in clinical research teams, often in hospitals or research organizations
Employer & Industry UsageUsed as entry-level training position in clinical research industryFull-time position responsible for managing clinical data collection and quality

The Clinical Data Management Internship provides foundational exposure to clinical data systems, ideal for students or recent graduates. In contrast, a Clinical Data Coordinator is a full-time role requiring more experience, focusing on managing and ensuring the quality of clinical data in research projects.

What are the most commonly searched types of Clinical Data Management jobs? The most popular types of Clinical Data Management jobs are:
Infographic showing various Clinical Data Management Internship job openings in the United States as of June 2026, with employment types broken down into 11% Internship, 73% Full Time, 11% Part Time, and 5% Contract. Highlights an 90% In-person, 5% Hybrid, and 5% Remote job distribution, with an average salary of $34,499 per year, or $16.6 per hour.
Senior Manager, Clinical Data Management

Senior Manager, Clinical Data Management

Stratacuity: Proven Scientific Placement

Watertown, MA

Other

Posted 9 days ago

Job description

Our Watertown based client is seeking a Senior Manager, Clinical Data Management to lead end‑to‑end clinical data management activities across our development programs. In this role, you will ensure high‑quality, reliable clinical data from study startup through database lock while providing strategic and operational leadership. You will collaborate closely with cross‑functional teams, oversee CROs and external vendors, and contribute to process optimization and inspection readiness as our organization continues to grow.

Key Responsibilities

  • Lead and oversee data management activities for assigned clinical trials from study startup through database lock.
  • Partner with CROs and vendors to develop and review Data Management Plans, CRF Completion Guidelines, CRF design, database/edit check specifications, data review plans, data transfer specifications, and database lock deliverables.
  • Oversee EDC systems and ensure data integrity, consistency, and quality throughout the clinical trial lifecycle.
  • Manage external data management vendors and CRO partners, including performance oversight, issue escalation, quality expectations, timelines, and budget considerations.
  • Lead data review and cleaning activities, including query management, reconciliation, external data integration, and risk identification.
  • Collaborate with Clinical Operations, Biostatistics, Statistical Programming, Clinical Development, Medical Monitoring, Safety, and Regulatory teams to resolve data‑related issues and support study deliverables.
  • Drive data management strategy to ensure alignment with clinical development goals and program timelines.
  • Develop, maintain, and enhance SOPs, templates, guidance documents, and best practices for clinical data management.
  • Identify operational risks and implement mitigation strategies to ensure inspection readiness and compliance with GCP, ICH, and regulatory requirements.
  • Support process improvement initiatives and contribute to building scalable, efficient data management operations.
  • Mentor junior team members and help strengthen data management capabilities across the organization.

Required Qualifications

  • Bachelor’s degree in a scientific, healthcare, or related field.
  • 8+ years of clinical data management experience in the pharmaceutical or biotechnology industry.
  • Proven experience independently leading data management activities across multiple clinical trials and/or programs.
  • Oncology clinical development experience strongly preferred.
  • Strong understanding of clinical trial processes, clinical data standards, GCP, ICH guidelines, and regulatory expectations.
  • Hands‑on experience with EDC systems, clinical databases, and related clinical technologies.
  • Experience managing CROs and external vendors, including oversight of deliverables, timelines, and quality.

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