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Clinical Data Management Intern Jobs in Texas (NOW HIRING)

Faeth Therapeutics

Clinical Data Manager

Austin, TX · On-site

$125K - $175K/yr

  • Medical

  • Dental

  • Vision

  • Retirement

Lead day-to-day data management activities for assigned clinical trials (Phase 2 and Phase 1b) * Oversee CRO and vendor data management deliverables to ensure timelines, quality, and compliance

Faeth Therapeutics

Clinical Data Manager

Austin, TX · Remote

$125K - $175K/yr

  • Medical

  • Dental

  • Vision

  • Retirement

Lead day-to-day data management activities for assigned clinical trials (Phase 2 and Phase 1b) * Oversee CRO and vendor data management deliverables to ensure timelines, quality, and compliance

City of Baytown

Emergency Management Intern

Baytown, TX · On-site

$13.75 - $18.25/hr

... updates, resource tracking, data management, and training exercises. The intern will work ... collaboratively with City departments and external partners to support preparedness initiatives ...

DiaSorin

Clinical Data Scientist

Austin, TX · On-site

... of clinical data management tools, database, and software for in vitro diagnostic products. The ... Manage the development of primary and validation programming and lead the report generation ...

DiaSorin

Clinical Data Scientist

Austin, TX · On-site

... of clinical data management tools, database, and software for in vitro diagnostic products. The ... Manage the development of primary and validation programming and lead the report generation ...

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Clinical Data Management Intern information

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.

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

The most popular types of Clinical Data Management jobs in Texas are:

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

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

What job categories do people searching Clinical Data Management Intern jobs in Texas look for?

The top searched job categories for Clinical Data Management Intern jobs in Texas are:

What cities in Texas are hiring for Clinical Data Management Intern jobs?

Cities in Texas with the most Clinical Data Management Intern job openings:

Clinical Data Management Intern jobs near you
Infographic showing various Clinical Data Management Intern job openings in Texas as of August 2026, with employment types broken down into 10% Internship, 71% Full Time, 9% Part Time, 5% Temporary, and 5% Contract. Highlights an 88% In-person, 2% Hybrid, and 10% Remote job distribution.

Clinical Data Manager

Faeth Therapeutics

Austin, TX • On-site

$125K - $175K/yr

Full-time

Medical, Dental, Vision, Retirement

Re-posted 29 days ago

Job description

Faeth Therapeutics is a clinical-stage oncology company listed on Nasdaq that recently raised $200M in funding. With a strong scientific foundation and a founding team that includes the discoverer of our target pathway, we are advancing PIKTOR, a multi-node PI3K/AKT/mTOR inhibitor program, toward multiple near-term milestones. We are a small, focused team where every person has direct impact - united by a shared commitment to care deeply, create boldly, and never stop learning.
Faeth Therapeutics is seeking an experienced Clinical Data Manager to support clinical data management activities across two active clinical trials. This individual will play a critical role in ensuring high-quality, reliable clinical data through the design, implementation, and oversight of data management processes. The role requires close collaboration with clinical operations, biostatistics, medical, and external vendors.
Reports to: Chief Medical Officer
Location: Remote (U.S.)
Responsibilities:
  • Lead day-to-day data management activities for assigned clinical trials (Phase 2 and Phase 1b)
  • Oversee CRO and vendor data management deliverables to ensure timelines, quality, and compliance
  • Review and contribute to key study documents, including:
  • Data Management Plans (DMPs)
  • Case Report Forms (CRFs) / eCRFs
  • Edit check specifications
  • Data transfer specifications
  • Manage database build, UAT, and database lock activities
  • Ensure data integrity, consistency, and completeness through ongoing data review and cleaning
  • Monitor query generation and resolution timelines
  • Perform data review, listings review, and support medical data review activities
  • Collaborate with biostatistics on data standards (e.g., CDISC/SDTM) and analysis datasets
  • Ensure compliance with GCP, regulatory requirements, and company SOPs
  • Support inspection readiness and participate in audits/inspections as needed
  • Contribute to process improvements and best practices in data management

Requirements:
  • Bachelor's degree in life sciences, computer science, or related field (advanced degree a plus)
  • 5-8 years of clinical data management experience in biotech, pharma, or CRO settings
  • Experience supporting early- to mid-phase clinical trials (Phase 1-2 required)
  • Hands-on experience with EDC systems (e.g., Medidata Rave, Veeva, Oracle InForm)
  • Strong understanding of clinical data standards (CDISC, SDTM)
  • Experience managing CROs and external vendors
  • Familiarity with oncology trials is preferred
  • Knowledge of GCP and regulatory requirements
  • Strong attention to detail and problem-solving skills
  • Excellent communication and cross-functional collaboration skills

Compensation Range: $125,000 - $175,000 (actual compensation may vary based on experience, qualifications and location)
Working at Faeth
Benefits:
  • Competitive salary and equity in a well-funded, clinical-stage biotech
  • 100% remote work and flexible schedule
  • Health, dental, and vision for you and your dependents
  • Flexible time off
  • Generous parental leave
  • Traditional and Roth 401k
  • Mission oriented, remote first culture

We are an equal opportunity employer, and we value diversity at our company. We do not discriminate on the basis of race, religion, color, national origin, gender, sexual orientation, age, marital status, veteran status, or disability status.
All offers of employment are contingent upon satisfactory completion of a background check and verification of eligibility to work in the United States.

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