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Clinical Data Management Internship Jobs (NOW HIRING)

Vedan Technologies

CA · On-site

Required Qualifications * 10+ years of experience in Clinical Data Management within pharma, biotech, or CRO environments. * Strong working knowledge of CDISC, SDTM, and ADaM standards . * Experience ...

Exelixis

Clinical Data Management Director

Alameda, CA · On-site

The Clinical Data Management (CDM) Director is a highly experienced and influential leader with expert knowledge of Clinical Data Management concepts and processes. This position is accountable for ...

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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.
Manager, Clinical Data Management

Manager, Clinical Data Management

Crispr Therapeutics

South Boston, MA • On-site

$123K - $133K/yr

Full-time

Posted 3 days ago

Job description

Job Description:
Company Overview
Since its inception over a decade ago, CRISPR Therapeutics has transformed from a research-stage company advancing programs in the field of gene editing, to a company with a diverse portfolio of product candidates across a broad range of disease areas including hemoglobinopathies, oncology, regenerative medicine, cardiovascular and rare diseases. The Nobel Prize-winning CRISPR science has revolutionized biomedical research and represents a powerful, clinically validated approach with the potential to create a new class of potentially transformative medicines. To accelerate and expand its efforts, CRISPR Therapeutics has established strategic partnerships with leading companies including Vertex Pharmaceuticals. CRISPR Therapeutics AG is headquartered in Zug, Switzerland, with its wholly-owned U.S. subsidiary, CRISPR Therapeutics, Inc., and R&D operations based in Boston, Massachusetts and San Francisco, California, and business offices in London, United Kingdom.
Position Summary
The Manager of Clinical Data Management will lead clinical data management activities in support of CRISPR studies across all stages of clinical development. They will ensure that clinical data capture, systems and processes will ensure accurate, consistent, high quality, and complete data.
The successful candidate will provide clinical data management oversight of outsourced clinical trials, including but not limited to: project management, vendor management, coordination of internal reviews, and approval of deliverables. The candidate will impact multiple clinical development programs, health authority submissions, presentations and publications across internal and external stakeholders.
Responsibilities
  • Plan, coordinate, and manage data management tasks and timelines.
  • Act as primary liaison with CROs, third party data vendors, and EDC vendors.
  • Collaborate with internal clinical study team to ensure all stakeholders' needs are addressed.
  • Primary author/approver for CRFs, CCGs, edit check specifications, SAE reconciliation plans, Coding plans, Data Management Plans, and third party vendor data specifications.
  • Oversee database design, production and UAT cycles, ensuring that the CRO meets the highest quality standards.
  • Accountable for external data vendor documentation, management, and reconciliation.
  • Contribute to departmental SOP and process development and improvement, and integration of technology.
  • Perform and/or review medical coding and SAE reconciliation.
  • Support internal review/QC of clinical data.
  • Support GCP inspection readiness.

Minimum Qualifications
  • Bachelor's degree in a health-related field is required, Master's degree strongly preferred
  • Minimum of 7+ years of progressive experience in clinical data management in a regulatory environment.
  • Demonstrated proficiency managing the lifecycle of clinical data projects.
  • Experience developing reports using J-Review, Business Objects, or other CDM reporting tools.
  • Experience with EDC databases, especially Medidata Rave.
  • Experience with CDASH/SDTM/CDISC standards.
  • Experience working with central and specialty labs/vendors.
  • Working knowledge of medical terminology and medical coding dictionaries including MedDRA and WHO.
  • Familiarity with GCP, ICH and FDA requirements as applicable for Clinical Data Management.
  • Ability to manage multiple initiatives and shifting priorities within a small, fast paced company environment.
  • Strong analytical and problem-solving skills that meet or improve the status quo.
  • Excellent interpersonal skills with the ability to work independently and collaboratively in a dynamic team environment.
  • Excellent written and oral communication skills.

Preferred Qualifications
  • Prior experience working in a small or medium-sized biotech or pharmaceutical company

Competencies
  • Collaborative - Openness, One Team
  • Undaunted - Fearless, Can-do attitude
  • Results Orientation - Delivering progress toward our mission. Sense of urgency in solving problems.
  • Entrepreneurial Spirit - Proactive. Ownership mindset.

CRISPR Therapeutics believes in fostering a dynamic workplace that balances remote work flexibility with the benefits of in-person interactions. Our employees work at least three days on-site, creating a collaborative work environment, where we cultivate mentorship opportunities, increase cross-functional communication and offer opportunities for our employees to connect. Certain lab based and manufacturing positions are located fully on-site.
Manager: Base pay range of $123,000 to $133,000+ bonus, equity and benefits
The range provided is CRISPR Therapeutics' reasonable estimate of the base compensation for this role. The actual amount will be based on job-related and non-discriminatory factors such as experience, training, skills, and abilities.
CRISPR Therapeutics, Inc. is committed to equal employment opportunity and non-discrimination for all employees and qualified applicants without regard to a person's race, color, gender, age, religion, national origin, ancestry, disability, veteran status, genetic information, sexual orientation or any characteristic protected under applicable law.
To view our Privacy Statement, please click the following link: http://www.crisprtx.com/about-us/privacy-policy

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