ZipRecruiter

Log In

1

Clinical Data Management Intern Jobs (NOW HIRING)

MSD

Specialists, Clinical Data Management

West Point, PA · On-site

$87K - $137K/yr

In this role, as a Clinical Data Management Specialist, you'll assumes the responsibilities for all clinical programming (including reporting and analytics) deliverables including Oracle, Veeva ...

Merck & Co.

$87K - $137K/yr

In this role, as a Clinical Data Management Specialist, you'll assumes the responsibilities for all clinical programming (including reporting and analytics) deliverables including Oracle, Veeva ...

Systimmune

Director, Clinical Data Management

Redmond, WA · On-site

$190K - $250K/yr

Lead and oversee the Clinical Data Management function, including strategy, standards, processes, and operational execution across the development portfolio. * Build and scale a high‑performing ...

Xencor

We have an excellent opportunity for a Director, Clinical Data Management , to join our team. This position will be based out of our San Diego, CA. office and is a minimum 2 days a week onsite hybrid ...

Xencor

Director, Clinical Data Management

San Diego, CA · On-site

We have an excellent opportunity for a Director, Clinical Data Management , to join our team. This position will be based out of our San Diego, CA. office and is a minimum 2 days a week onsite hybrid ...

Nuvation Bio, Inc.

Director, Clinical Data Management

NY · On-site +1

$220K - $230K/yr

Serve as the primary data management lead for assigned clinical trials, ensuring timely, high-quality data deliverables throughout the data lifecycle. * Develop and maintain study-specific data ...

Nuvation Bio, Inc.

Director, Clinical Data Management

NY · Remote

$220K - $230K/yr

Serve as the primary data management lead for assigned clinical trials, ensuring timely, high-quality data deliverables throughout the data lifecycle. * Develop and maintain study-specific data ...

previous pagenext page

Showing results 21-40

All JobsClinical Data Management Intern Jobs

Clinical Data Management Intern information

See salary details

$12

$22

$42

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

As of Sep 15, 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 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 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 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 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.

More about Clinical Data Management Intern jobs

What cities are hiring for Clinical Data Management Intern jobs?

Cities with the most Clinical Data Management Intern job openings:

What are the most commonly searched types of Clinical Data Management jobs?

The most popular types of Clinical Data Management jobs are:

What states have the most Clinical Data Management Intern jobs?

States with the most job openings for Clinical Data Management Intern jobs include:

What are popular job titles related to Clinical Data Management Intern jobs?

For Clinical Data Management Intern jobs, the most frequently searched job titles are:

Clinical Data Management Intern jobs near you
Infographic showing various Clinical Data Management Intern job openings in the United States as of September 2026, with employment types broken down into 1% As Needed, 83% Full Time, 14% Part Time, and 2% Contract. Highlights an 82% Physical, 2% Hybrid, and 16% Remote job distribution, with an average salary of $46,809 per year, or $22.5 per hour.

Director, Clinical Data Management

Warren, NJ • On-site

PTC Therapeutics
Manufacturing • 501 - 1,000 employees
Learn more about PTC Therapeuticsexternal

Full-time

Medical, Dental, Vision, Retirement

Re-posted 20 days ago

Job description

PTC Therapeutics is a global commercial biopharmaceutical company. For over 25 years our team has been deeply committed to a unified purpose: Extending life's moments for children and adults living with a rare disease.
At PTC, we cultivate an inclusive culture where everyone feels valued, respected, and empowered. We welcome candidates from all backgrounds to join our team, fostering a strong sense of belonging.
Visit our website to learn more about our company and culture!
Site: www.ptcbio.com
Job Description Summary:
Job Description:
Candidates local to the Warren, NJ area are strongly preferred for our flexible hybrid work model. We welcome applicants who are open to relocating to the area.
The Director, Clinical Data Management provides strategic and operational leadership and oversight of data management activities to ensure the quality, integrity, consistency and inspection readiness of clinical databases for subsequent analysis, reporting and regulatory submissions. This position has a leadership role to proactively develop plans for the utilization of EDC system processes and other clinical data applications that allow for internal control of clinical databases. This position will lead/contribute in defining Sponsor processes and procedures for maintaining clinical data and the associated Quality Assurance (QA) Quality Control (QC) documentation.
She/He may have supervisory responsibilities for both internal staff and external consultants and may manage direct reports.
The incumbent works cross-functionally with various internal departments and external resources on Data Management related issues.
The Director, Clinical Data Management, ensures adherence to relevant regulatory requirements and company Standard Operating Procedures (SOPs) as appropriate.
ESSENTIAL FUNCTIONS
Primary duties/responsibilities:
  • Ensure the data collected meets the requirements of the study objective and company quality standards.
  • Drives the development and implementation of strategic vision for data management (DM) group.
  • Provide functional oversight of CROs to prepare and ensure proper execution of data management plans and manage data management projects from beginning to end.
  • Partners with Clinical Operations group, biostatisticians, SAS programmers and other staff as appropriate to design and develop data collection instruments (e.g., eCRF's) to ensure the required information is captured for statistical analysis.
  • Oversee and as needed, directly support coding review for adverse events, medical history and concomitant medications and coordinate medical monitor review and approval of medical coding
  • Lead data management activities, clinical database cleaning in EDC, data reconciliation with external vendor data, SAE reconciliation and lock activities.
  • Lead development of data management plans, data review plans, supervise database development, and reviewing and processing of clinical trial data to ensure completeness, accuracy, and consistency of clinical trials data.
  • Prepare and distribute or facilitate distribution of periodic reports of study status including, case report form (CRF) completion status, missing pages, query aging, clean patient tracker (CPT), etc.
  • Participate in cross functional team meetings, as requested, and communicate with all departments regarding project statuses/issues, provide ongoing feedback on data management workflows to increase efficiency and provide feedback to CRAs.
  • Lead interactions with outside vendors (e.g., clinical laboratories) on collection, transmittal, and transfer of study specific data.
  • Develop and update SOP's and other documents associated with the data collection, handling, and review processes, e.g., Working Instructions (WI), Best Practices Documents (BPD)to meet regulatory compliance and operational needs.
  • Facilitates and contributes to regulatory submissions and audit/inspection activities.
  • Gathers requirements related to existing clinical systems to identify opportunities to enhance, improve and streamline processes and systems use.
  • Leads the assessment and selection of Data Management vendors and systems for clinical data collection and analysis.
  • Participate in clinical review and validation of statistical outputs used in the preparation of final reports.
  • Mentor clinical team members by resolving problems and providing DM guidance.
  • Manage multiple and varied tasks, prioritize workload with attention to detail.
  • Understand the legal and compliance environment and drive collaboration with the Legal and Compliance team.
  • Drive the spirit of "ONE Team" across all functions by supporting a team approach to focus on our patients and customers as our top priorities.
  • Lead the completion of data management activities to meet project timelines and communicate status to respective team members.
  • Contribute to the development of outsourcing strategies and relationships with outsourcing partner and may play a role in identification of quality DM partners including coordinating the review and approval of the Master Services Agreement.
  • May manage, coach, and mentor direct reports.
  • Performs other tasks and assignments as needed and specified by management.

KNOWLEDGE/SKILLS/ABILITIES REQUIRED
* Minimum level of education and years of relevant work experience.
  • Bachelor's degree in science or related field (such as healthcare) and a minimum of 10 years of relevant progressively responsible experience in a pharmaceutical, biotech, CRO, or Regulatory Agency with an emphasis on building data collection and assimilation solutions.

* Special knowledge or skills needed and/or licenses or certificates required.
  • A proven track record of successful leadership of data management team(s). Previous leadership of vendor management experience using Interactive Web Response System (IWRS), Imaging, Patient Reported Outcome (ePRO/eCOA) and other database technologies.
  • Highly detail oriented while maintaining work efficiency, able to prioritize activities across various projects at different study stages.
  • Knowledge of industry standards, such as the ICH guidelines, CDASH, 21 CFR Part 11, and FDA guidelines.
  • Understanding of drug development process and data operations required for the reporting of clinical trial data (e.g., data review, study reports, regulatory submissions, safety updates, etc.).
  • Strong verbal and written communication, decision-making, influencing, negotiation, and project management skills.
  • Technical skills and experience using Medidata or relational databases (e.g., Oracle RDC, InForm, Veeva EDC) and data visualization tools (e.g., Spotfire, J-Review, Business Objects).
  • Proficiency in the use of Microsoft Office Suite of tools (Word, Excel, etc.).
  • Learning agility and 'scalability' to take on increasing responsibility Excellent time management, flexibility, ability to coordinate workload and meet established deadlines.
  • Ability to influence without direct authority.
  • Demonstrated leadership ability and experience managing, coaching, and mentoring direct reports.
  • Ability to work independently and collaboratively, as required, in a fast-paced, matrixed, team environment consisting of internal and external team members.
  • Analytical thinker with excellent problem-solving skills and the ability to adapt to changing priorities and deadlines.
  • Excellent planning, organization and time management skills including the ability to support and prioritize multiple projects.
  • Knowledge of different regulatory standards and requirements, including but not limited to FDA, EMEA, and PMDA.

*Special knowledge or skills and/or licenses or certificates preferred.
  • Minimum five (5) years' experience with Medidata RAVE (EDC, R2DS/RBS, Architect, Coder).
  • Strong understanding and application of regulatory requirements and relevant data standards; CDISC knowledge and experience.
  • Experience in PL/SQL, SAS, Java, C++ relational database design and database programming skills preferred.
  • Understanding of Compliance and Regulations, such as ICH, GxP, Annex 11, GDPR and GAMP.
  • Understanding of the use of risk-based approach for process efficiency and compliance.
  • Clinical Data Interchange Standards Consortium (CDISC) experience.

* Travel requirements
  • 25%

Expected Base Salary Range
$200,700 - 252,600. The base salary offered will be contingent on assessment of candidate education level, background, and experience relative to the requirements of the position they are being considered for, as well as review of internal equity.
In addition to base salary, PTC employees are also eligible for short- and long-term incentives. All eligible employees may also enroll in PTC's medical, dental, vision, and retirement savings plans.
EEO Statement:
PTC Therapeutics is an equal opportunity employer. We welcome applications from all individuals, regardless of race, color, national origin, gender, age, physical characteristics, social origin, disability, religion, family status, pregnancy, sexual orientation, gender identity, gender expression, disability, veteran status or any unlawful criterion under applicable law. We are committed to treating all applicants fairly and avoiding discrimination.
Click here to return to the careers page

Apply