ZipRecruiter

Log In

2

Clinical Data Associate Remote Jobs in Texas (NOW HIRING)

Faeth Therapeutics

Senior Clinical Scientist

Austin, TX · Remote

$150K - $200K/yr

Remote (U.S.) Responsibilities: * Lead the design and development of clinical protocols, amendments ... Drive data quality, including oversight of data cleaning, query resolution, and database lock

NTT DATA Services

Ontology Expert - Remote

Dallas, TX · Remote

... with clinicians, data scientists, and AI engineers to translate knowledge into formal models ... The starting pay range for this remote role is $105,840.00-$147,000.00. This range reflects the ...

NTT DATA Services

Ontology Expert - Remote

Dallas, TX · On-site +1

... with clinicians, data scientists, and AI engineers to translate knowledge into formal models ... The starting pay range for this remote role is $105,840.00-$147,000.00. This range reflects the ...

NTT DATA Services

Ontology Expert - Remote

Dallas, TX · Remote

... with clinicians, data scientists, and AI engineers to translate knowledge into formal models ... The starting pay range for this remote role is $105,840.00-$147,000.00. This range reflects the ...

Faeth Therapeutics

VP, Clinical Development

Austin, TX · Remote

Remote (U.S.) Responsibilities: Clinical Development Strategy & Medical Leadership * Lead the ... Clinical Data Review & Scientific Oversight * Lead ongoing review and interpretation of clinical ...

previous pagenext page

Showing results 21-40

All JobsClinical Data Associate JobsClinical Data Associate Remote JobsClinical Data Associate Remote Jobs in Texas

Clinical Data Associate Remote information

See Texas salary details

$11

$37

$80

How much do clinical data associate remote jobs pay per hour?

As of Aug 11, 2026, the average hourly pay for clinical data associate remote in Texas is $37.48, according to ZipRecruiter salary data. Most workers in this role earn between $26.25 and $46.97 per hour, depending on experience, location, and employer.

What are some common challenges faced by a clinical data associate working remotely, and how can they be managed?

Clinical Data Associates working remotely often face challenges related to communication and maintaining data quality standards across distributed teams. It can be more difficult to collaborate with clinical research coordinators, data managers, and other stakeholders without in-person interactions, making clear and timely communication essential. Utilizing secure data management platforms, participating in regular virtual meetings, and adhering strictly to data integrity protocols can help address these challenges. Proactively seeking feedback and staying updated on regulatory changes also contribute to maintaining high standards while working remotely.

What is a clinical data associate?

A Clinical Data Associate (Remote) is a professional who manages and verifies data collected during clinical trials, working from a remote location. They ensure the accuracy, integrity, and confidentiality of clinical trial data, collaborating with clinical teams and using specialized software. Their responsibilities include data entry, cleaning, validation, and generating reports to support regulatory submissions. Remote Clinical Data Associates utilize secure systems to access and manage data, allowing them to efficiently support clinical research from anywhere.

What are the key skills and qualifications needed to thrive as a clinical data associate?

To thrive as a Clinical Data Associate (Remote), you need a strong background in life sciences, data management, and an understanding of clinical trial processes, often supported by a relevant bachelor's degree. Familiarity with electronic data capture (EDC) systems, clinical data management software, and GCP (Good Clinical Practice) certification are commonly required. Attention to detail, problem-solving abilities, and effective virtual communication are crucial soft skills for managing data integrity and collaborating with remote teams. These skills and qualifications ensure the accurate collection, validation, and reporting of clinical trial data, which is essential for regulatory compliance and successful study outcomes.

What is the difference between Clinical Data Associate Remote vs Clinical Data Coordinator?

AspectClinical Data Associate RemoteClinical Data Coordinator
CredentialsBachelor's in life sciences or related field; familiarity with data management systemsBachelor's in health sciences or related field; experience with clinical data
Work EnvironmentRemote, primarily computer-basedTypically on-site or hybrid, working with clinical teams
Employer & IndustryPharmaceutical companies, CROs, biotech firmsHospitals, research institutions, clinical trial sites
Search & Comparison IntentYesYes

The Clinical Data Associate Remote and Clinical Data Coordinator roles share similarities in required education and industry usage. However, Clinical Data Associate Remote positions are primarily remote and focus on data entry and management from a distance, while Clinical Data Coordinators often work on-site, coordinating data collection and quality at clinical sites. Both roles are essential in clinical research but differ mainly in work setting and specific responsibilities.

What are popular job titles related to Clinical Data Associate Remote jobs in Texas? For Clinical Data Associate Remote jobs in Texas, the most frequently searched job titles are:
What job categories do people searching Clinical Data Associate Remote jobs in Texas look for? The top searched job categories for Clinical Data Associate Remote jobs in Texas are:
What cities in Texas are hiring for Clinical Data Associate Remote jobs? Cities in Texas with the most Clinical Data Associate Remote job openings:
Clinical Data Associate Remote jobs near you
Infographic showing various Clinical Data Associate Remote job openings in Texas as of August 2026, with employment types broken down into 76% Full Time, 17% Part Time, and 7% Contract. Highlights an 2% Hybrid, and 98% Remote job distribution, with an average salary of $77,954 per year, or $37.5 per hour.

Senior Clinical Scientist

Faeth Therapeutics

Austin, TX • Remote

$150K - $200K/yr

Full-time

Medical, Dental, Vision, Life, Retirement

Re-posted 21 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 the PI3K pathway, we are advancing PIKTOR, a multi-node PI3K/AKT/mTOR inhibitor program, into late stage development. 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.

The Senior Clinical Scientist is a key scientific leader within the Clinical Development team, responsible for the design, execution, and interpretation of clinical trials across Faeth's oncology programs. This individual will drive cross-functional collaboration, provide strategic input into clinical development plans, and ensure delivery of high-quality data to support regulatory and scientific objectives. The role requires deep scientific expertise, operational insight, and the ability to influence both internal and external stakeholders.

Reports to: CMO

Location: Remote (U.S.)

Responsibilities:

  • Lead the design and development of clinical protocols, amendments, and core study documents (e.g.,IBs, DSURs, SAPs, CRFs)
  • Lead ongoing review, monitoring, querying and interpretation of clinical data (safety, efficacy, PK/PD, and biomarker endpoints)
  • Provide leadership across one or more clinical programs, including lifecycle planning
  • Oversee execution of Phase 1-3 clinical trials in partnership with Clinical Operations, ensuring quality, timelines, and clinical review of data
  • Serve as a primary clinical point of contact for CROs, vendors, and investigative sites
  • Identify and proactively mitigate study risks; drive issue resolution across functions
  • Drive data quality, including oversight of data cleaning, query resolution, and database lock
  • Ensure alignment between clinical strategy and translational/biomarker plans
  • Lead contributions to regulatory submissions (INDs, CTAs, briefing documents, responses to health authorities)
  • Drive preparation of clinical study reports (CSRs), abstracts, manuscripts, and conference presentations
  • Represent Clinical Development in internal governance meetings and external interactions

Requirements:

  • 5-8+ years of oncology clinical development experience
  • Demonstrated experience leading components of interventional clinical trials (Phase 1-3)
  • Strong expertise in clinical trial design, execution, and data interpretation
  • Deep understanding of oncology drug development; experience in metabolism, nutrition, or biomarker-driven approaches is a plus
  • Working knowledge of GCP, ICH guidelines, and global regulatory requirements
  • Proven ability to lead cross-functional initiatives and influence without authority
  • Excellent communication, analytical, and problem-solving skills
  • Comfortable operating in a fast-paced, evolving biotech environment

Preferred:

  • Advanced degree (PhD, PharmD, MS, or equivalent) in life sciences, clinical research, or related field

Compensation Range: $150,000 - $200,000 (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