ZipRecruiter

Log In

1

Clinical Data Monitor Jobs in Texas (NOW HIRING)

Faeth Therapeutics

Clinical Data Manager

Austin, TX · On-site

$125K - $175K/yr

Faeth Therapeutics is a clinical-stage oncology company listed on Nasdaq that recently raised $200M ... Monitor query generation and resolution timelines * Perform data review, listings review, and ...

Faeth Therapeutics

Clinical Data Manager

Austin, TX · Remote

$125K - $175K/yr

Faeth Therapeutics is a clinical-stage oncology company listed on Nasdaq that recently raised $200M ... Monitor query generation and resolution timelines * Perform data review, listings review, and ...

DiaSorin

Clinical Data Scientist

Austin, TX

Responsible for monitoring assigned clinical and outcomes studies to ensure compliance with ... Clinical data entry and QC * Case Report Form (CRF) and query management * Select, validate, manage ...

DiaSorin

Clinical Data Scientist

Austin, TX · On-site

Responsible for monitoring assigned clinical and outcomes studies to ensure compliance with ... Clinical data entry and QC * Case Report Form (CRF) and query management * Select, validate, manage ...

Faeth Therapeutics

VP, Clinical Development

Austin, TX · On-site

... Monitor for interventional oncology clinical trials. * Demonstrated experience leading cross-functional clinical development teams. * Experience interpreting clinical data and guiding development ...

Faeth Therapeutics

VP, Clinical Development

Austin, TX · Remote

... Monitor for interventional oncology clinical trials. * Demonstrated experience leading cross-functional clinical development teams. * Experience interpreting clinical data and guiding development ...

next page

Showing results 1-20

All JobsClinical Data Monitor JobsClinical Data Monitor Jobs in Texas

Clinical Data Monitor information

What is a clinical data monitor?

A Clinical Data Monitor is a professional responsible for overseeing the accuracy, integrity, and security of data collected during clinical trials. They ensure that clinical trial data is collected, entered, and reported according to regulatory standards and study protocols. Their work helps maintain the quality of data used to assess the safety and effectiveness of new drugs or medical devices. Clinical Data Monitors often collaborate with clinical research coordinators, data managers, and regulatory authorities to ensure compliance and resolve any data discrepancies.

How does a clinical data monitor typically interact with other teams during a clinical trial?

Clinical Data Monitors work closely with various teams such as clinical research associates (CRAs), data management, and biostatistics. They are responsible for ensuring the accuracy and integrity of clinical trial data by regularly reviewing case report forms and addressing discrepancies with site staff and data managers. Effective communication and collaboration are crucial, as Clinical Data Monitors often need to provide feedback, clarify data inconsistencies, and ensure all regulatory and protocol requirements are met throughout the trial.

How to become a clinical data monitor?

To become a clinical data monitor, typically a bachelor's degree in health sciences, life sciences, or a related field is required. Relevant skills include knowledge of clinical trial processes, data management, and familiarity with electronic data capture systems; obtaining certifications like the Society of Clinical Data Management (SCDM) certification can enhance prospects. Gaining experience through internships or entry-level roles in clinical research is also beneficial.

What are the key skills and qualifications needed to thrive as a clinical data monitor, and why are they important?

To thrive as a Clinical Data Monitor, you need a solid understanding of clinical research processes, data management, and regulatory compliance, often supported by a degree in life sciences or a related field. Familiarity with clinical trial management systems (CTMS), electronic data capture (EDC) platforms, and knowledge of Good Clinical Practice (GCP) guidelines are typically required. Attention to detail, analytical thinking, and strong communication skills set outstanding professionals apart in this role. These skills are crucial to ensure the accuracy, integrity, and regulatory compliance of clinical trial data, which supports successful drug development and patient safety.

What is the difference between Clinical Data Monitor vs Clinical Data Coordinator?

AspectClinical Data MonitorClinical Data Coordinator
CredentialsTypically requires a degree in life sciences or healthcare, often with certifications like CDMP or CDISCUsually holds a degree in health sciences or related field, with similar certifications
Work EnvironmentWorks primarily on data review, monitoring clinical trial sites, and ensuring data qualityHandles data entry, management, and coordination between sites and sponsors
Employer & IndustryPharmaceutical companies, CROs, biotech firmsResearch organizations, hospitals, clinical trial sites

The Clinical Data Monitor focuses on reviewing and verifying clinical trial data to ensure accuracy and compliance, often working directly with sites. The Clinical Data Coordinator manages data entry and organization, supporting the data collection process. Both roles require similar educational backgrounds and certifications but differ in daily responsibilities and focus areas.

What are popular job titles related to Clinical Data Monitor jobs in Texas? For Clinical Data Monitor jobs in Texas, the most frequently searched job titles are:
What job categories do people searching Clinical Data Monitor jobs in Texas look for? The top searched job categories for Clinical Data Monitor jobs in Texas are:
Clinical Data Monitor jobs near you
Infographic showing various Clinical Data Monitor job openings in Texas as of August 2026, with employment types broken down into 1% As Needed, 86% Full Time, 10% Part Time, and 3% Contract. Highlights an 86% Physical, 4% 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 25 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.

Apply