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Clinical Data Management Intern Jobs (NOW HIRING)

Abbott

Clinical Data Management Analyst

Alameda, CA · On-site

$81.50K - $141.30K/yr

The Opportunity The Clinical Data Management Analyst will be an individual contributor that works under limited supervision and applies subject matter knowledge. Requires the capacity to understand ...

Abbott

Clinical Data Management Analyst

Alameda, CA · On-site

$81.50K - $141.30K/yr

The Opportunity The Clinical Data Management Analyst will be an individual contributor that works under limited supervision and applies subject matter knowledge. Requires the capacity to understand ...

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 Intern information

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

As of May 31, 2026, the average hourly pay for clinical data management intern in the United States is $22.50, according to ZipRecruiter salary data. Most workers in this role earn between $17.31 and $24.52 per hour, depending on experience, location, and employer.

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

To excel as a Clinical Data Management Intern, you need a solid understanding of clinical research concepts, attention to detail, and at least a bachelor's degree in life sciences or related fields. Familiarity with data management tools like Oracle Clinical, Medidata Rave, and basic knowledge of regulatory standards such as GCP are highly valuable. Strong organizational skills, analytical thinking, and effective communication help you collaborate with cross-functional teams and maintain data integrity. These skills are crucial for ensuring accurate, compliant, and reliable clinical data that supports successful research outcomes.

What kinds of projects or tasks can a Clinical Data Management Intern expect to work on during their internship?

As a Clinical Data Management Intern, you can anticipate supporting tasks such as reviewing clinical trial data for accuracy, assisting with database setup and validation, and ensuring data is entered and managed according to protocols. You'll often collaborate closely with data managers, statisticians, and clinical research teams to help maintain data integrity and compliance with regulatory standards. This hands-on experience provides valuable exposure to industry tools and processes, which is a strong foundation for advancing into more specialized roles within clinical research.

What does a Clinical Data Management Intern do?

A Clinical Data Management Intern assists in the collection, organization, and validation of clinical trial data to ensure its accuracy and integrity. They support senior data managers by performing data entry, cleaning datasets, conducting quality checks, and generating reports. Interns often learn about regulatory requirements, data management systems, and Good Clinical Practice (GCP) guidelines. Their work is crucial for ensuring that clinical trial results are reliable and meet industry standards.

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

AspectClinical Data Management InternClinical Data Coordinator
Required CredentialsTypically pursuing or recent graduate in life sciences or related fieldBachelor's degree in life sciences, health informatics, or related field
Work EnvironmentInternship setting, often in pharmaceutical or biotech companiesFull-time role in clinical research teams, often in hospitals or research organizations
Employer & Industry UsageUsed in pharmaceutical, biotech, and clinical research companies for entry-level rolesCommon in clinical research organizations, hospitals, and pharmaceutical companies

The Clinical Data Management Intern typically is a temporary, entry-level position aimed at gaining experience in clinical data processes, while the Clinical Data Coordinator is a full-time role responsible for managing and ensuring the quality of clinical data during trials. Both roles require knowledge of data management principles, but the intern position is more educational, whereas the coordinator role involves more responsibility and hands-on data oversight.

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Clinical Data Management Intern jobs near you
Infographic showing various Clinical Data Management Intern job openings in the United States as of May 2026, with employment types broken down into 89% Full Time, 4% Temporary, and 7% Contract. Highlights an 74% Physical, 5% Hybrid, and 21% Remote job distribution, with an average salary of $46,809 per year, or $22.5 per hour.
Director, Clinical Data Management

Director, Clinical Data Management

Syndax Pharmaceuticals

New York, NY • On-site

$220K - $250K/yr

Full-time

Posted 5 days ago

Job description

Syndax Pharmaceuticals is looking for a Director, Clinical Data Management
At Syndax, we are determined to realize a future in which people with cancer live longer and better than ever before. Syndax Pharmaceuticals is a commercial stage biopharmaceutical company developing an innovative pipeline of cancer therapies.
The Role:
This position is a strategic leader responsible for overseeing the design, implementation, and oversight of clinical data systems and processes across multiple clinical development programs. This role directs a team in delivering high-quality clinical data in alignment with regulatory requirements, corporate goals, and operational efficiency. The Director contributes to the long-term success of the function through data-driven strategies, innovation in systems and processes, and strong cross-functional partnerships. May also be responsible for projects that have been contracted with a service provider, as well as internal projects.
Key Responsibilities:
  • Collaborate with senior leadership to define and implement functional and organizational strategy aligned with corporate objectives; participate in long-term planning and policy development.
  • Development and execution of data quality strategies, risk-based data review plans, and cross-study harmonization.
  • Direct the design, testing, validation, and maintenance of clinical databases and electronic data capture (EDC) systems.
  • Ensure consistent application of CDM standards, tools (e.g., CDISC, Medidata Rave), and procedures.
  • Oversee issue resolution and data integrity across outsourced vendors and internal teams.
  • Provide proactive input into clinical protocol design to ensure data collection strategies align with scientific and regulatory requirements.
  • Review and contribute to clinical protocols and statistical analysis plans to ensure alignment with data collection objectives; cross-project consistency and standardization of case report forms.
  • Partner with internal stakeholders to align timelines and data delivery requirements.
  • Participate in cross-functional study teams; influence protocol design, study setup, and data strategy from study start to submission.
  • Actively support submission readiness, including data integration and final deliverables for regulatory filings.
  • Participate in protocol development, clinical study reports (CSR), and submission activities.
  • Manage relationships with CROs and third-party vendors, ensuring alignment with contractual deliverables and performance expectations.
  • Establish standards and oversight processes for EDC setup, CRF development, data validation, discrepancy management, and database lock.
  • Drive consistency and scalability through implementation of standards (e.g., CDISC/CDASH/SDTM) and SOPs.
  • Development and improvement of clinical data management processes and tools.
  • Lead and mentor Clinical Data Managers; provide coaching and foster a high-performing and collaborative environment.
  • Participates in the evaluation of organizational needs, defining resource strategies, and managing departmental budgets and headcount planning.

Desired Experience/Education and Personal Attributes:
  • Bachelor's degree in related scientific discipline; advanced degree preferred.
  • 12+ years of progressive experience in clinical data management with leadership responsibility at a sponsor organization.
  • Expert knowledge of clinical data management.
  • Deep expertise of industry standards including CDISC/CDASH, SDTM, ICH-GCP, 21 CFR Part 11, and regulatory submission requirements.
  • Proven success leading large-scale global studies, vendor oversight and working in both in-house and outsourced models.
  • Expertise knowledge and hands on experience with EDC systems (e.g., Medidata Rave, Veeva), clinical systems integration, and risk-based monitoring frameworks required.
  • Exceptional leadership, analytical, and communication skills with the ability to influence senior stakeholders and executives.

Location: Syndax's corporate office is in New York, NY.
Syndax offers a total compensation and rewards package that is among the most competitive in the industry. Base pay is just one element of our package and is determined within a range based on several factors including market data, experience, qualifications, demonstrated skills, relevant education or training, travel requirements and internal equity. Our overall package also includes an equity offering, annual target bonuses, and an outstanding benefits program. The anticipated annualized salary range for this role is: $220,000 - 250,000.
About Syndax:
Syndax Pharmaceuticals is a commercial-stage biopharmaceutical company advancing innovative cancer therapies. Highlights of the Company's pipeline include a menin inhibitor for R/R acute leukemia and a monoclonal antibody that blocks the CSF-1 receptor for chronic graft-versus-host disease. Fueled by our commitment to reimagining cancer care, Syndax is working to unlock the full potential of its pipeline and is conducting several clinical trials across the continuum of treatment. For more information, please visit www.syndax.com/ or follow the Company on X and LinkedIn.
Syndax Pharmaceuticals is an equal opportunity employer and will not discriminate against any employee or applicant on the basis of age, color, disability, gender, national origin, race, religion, sexual orientation, veteran status, or any classification protected by federal, state, or local law.
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