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Clinical Development Jobs in Texas (NOW HIRING)

Faeth Therapeutics

VP, Clinical Development

Austin, TX · On-site

The Vice President, Clinical Development will provide strategic and medical leadership across middle and late stage development for Faeth's oncology portfolio. This executive will serve as the senior ...

Faeth Therapeutics

VP, Clinical Development

Austin, TX · Remote

The Vice President, Clinical Development will provide strategic and medical leadership across middle and late stage development for Faeth's oncology portfolio. This executive will serve as the senior ...

Faeth Therapeutics

Senior Clinical Scientist

Austin, TX · Remote

$150K - $200K/yr

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 ...

Faeth Therapeutics

Senior Clinical Scientist

Austin, TX · On-site

$150K - $200K/yr

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 ...

Medpace, Inc.

Clinical Informatics Analyst

Irving, TX · On-site

Our mission is to accelerate the global development of safe and effective medical therapeutics through the advancement of clinical research. We leverage in-country regulatory and therapeutic ...

New

Medpace, Inc.

Clinical Informatics Analyst

Irving, TX · On-site +1

Our mission is to accelerate the global development of safe and effective medical therapeutics through the advancement of clinical research. We leverage in-country regulatory and therapeutic ...

New

DiaSorin

Clinical Data Scientist

Austin, TX · On-site

Job Scope This position plays an integral role in the development, sourcing and maintenance of clinical data management tools, database, and software for in vitro diagnostic products. The role ...

DiaSorin

Clinical Data Scientist

Austin, TX · On-site

Job Scope This position plays an integral role in the development, sourcing and maintenance of clinical data management tools, database, and software for in vitro diagnostic products. The role ...

Laekna LLC

Head of Business Development

Dallas, TX · On-site

On the other hand, the company's self-developed innovative drugs will soon enter clinical ... development stages. Laekna's leadership team possesses over 20 years of experience in new drug ...

Laekna LLC

Head of Business Development

Dallas, TX

On the other hand, the company's self-developed innovative drugs will soon enter clinical ... development stages. Laekna's leadership team possesses over 20 years of experience in new drug ...

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All JobsClinical Development JobsClinical Development Jobs in Texas

Clinical Development information

See Texas salary details

$13

$32

$83

How much do clinical development jobs pay per hour?

As of Aug 8, 2026, the average hourly pay for clinical development in Texas is $32.25, according to ZipRecruiter salary data. Most workers in this role earn between $15.43 and $30.67 per hour, depending on experience, location, and employer.

What is the difference between Clinical Development vs Clinical Research Coordinator?

AspectClinical DevelopmentClinical Research Coordinator
Required CredentialsBachelor's degree, often advanced degrees in life sciences or related fields; certifications like CCRP or RACBachelor's degree in health sciences or related field; certifications like CCRP beneficial
Work EnvironmentPharmaceutical or biotech companies, clinical trial teams, R&D departmentsClinical trial sites, hospitals, research centers
Employer & Industry UsageUsed in pharmaceutical, biotech, and medical device industries during drug development phasesUsed in hospitals, research institutions, and clinical trial sites for managing patient studies

While both roles are involved in clinical trials, Clinical Development focuses on designing and managing the overall drug development process, whereas Clinical Research Coordinators handle the day-to-day operations at trial sites, ensuring protocol adherence and patient coordination.

What is clinical development?

Clinical development is the process by which new pharmaceutical drugs, biologics, or medical devices are tested and evaluated in humans to assess their safety and effectiveness. It typically involves a series of phases (Phase I-IV) of clinical trials, starting with small groups of volunteers and expanding to larger patient populations. The goal is to gather the data needed for regulatory approval and to ensure that new treatments provide benefits that outweigh their risks. Clinical development is a critical step in bringing new therapies from the laboratory to patients.

What do you do in clinical development?

A professional in clinical development designs, manages, and oversees clinical trials to evaluate the safety and effectiveness of new medical treatments or drugs. They coordinate with cross-functional teams, ensure compliance with regulatory standards, and analyze data to support product approval processes. Strong project management skills and knowledge of Good Clinical Practice (GCP) are essential in this role.

What does a clinical development specialist do?

A clinical development specialist designs, manages, and oversees clinical trials to evaluate the safety and effectiveness of new medical treatments or devices. They coordinate with research teams, ensure compliance with regulatory requirements, and analyze data to support product approval processes. Strong knowledge of Good Clinical Practice (GCP) and clinical trial management systems is essential for this role.

What are the key skills and qualifications needed to thrive in clinical development?

To thrive in Clinical Development, you need a strong background in life sciences, clinical trial management, and regulatory compliance, often supported by a relevant degree and experience in clinical research. Familiarity with clinical trial management systems (CTMS), electronic data capture (EDC) tools, and certifications like GCP (Good Clinical Practice) are typically required. Excellent communication, problem-solving, and leadership skills help professionals coordinate multidisciplinary teams and adapt to evolving study demands. These skills and qualifications ensure the design, execution, and oversight of safe, effective, and compliant clinical trials essential for successful drug development.

What are some common challenges faced in a clinical development role, and how can I prepare for them?

Professionals in Clinical Development often encounter challenges such as managing complex regulatory requirements, coordinating multi-site clinical trials, and ensuring timely patient recruitment. Staying organized, maintaining clear communication with cross-functional teams, and keeping up-to-date with evolving industry guidelines can help you navigate these hurdles. Developing strong project management and problem-solving skills is also essential for success in this dynamic field.
What are the most commonly searched types of Clinical Development jobs in Texas? The most popular types of Clinical Development jobs in Texas are:
What are popular job titles related to Clinical Development jobs in Texas? For Clinical Development jobs in Texas, the most frequently searched job titles are:
What job categories do people searching Clinical Development jobs in Texas look for? The top searched job categories for Clinical Development jobs in Texas are:
What cities in Texas are hiring for Clinical Development jobs? Cities in Texas with the most Clinical Development job openings:
Clinical Development jobs near you
Infographic showing various Clinical Development job openings in Texas as of August 2026, with employment types broken down into 1% As Needed, 81% Full Time, 15% Part Time, and 3% Contract. Highlights an 92% Physical, 2% Hybrid, and 6% Remote job distribution, with an average salary of $67,081 per year, or $32.3 per hour.

VP, Clinical Development

Faeth Therapeutics

Austin, TX • On-site

Full-time

Medical, Dental, Vision, Retirement

Re-posted 20 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.
The Vice President, Clinical Development will provide strategic and medical leadership across middle and late stage development for Faeth's oncology portfolio. This executive will serve as the senior medical leader for assigned programs, driving clinical strategy, providing medical oversight, and partnering cross-functionally to advance programs from late-stage development through regulatory approval.
This is a highly visible leadership role within a small, fast-paced biotechnology company where the successful candidate will influence company strategy, work directly with executive leadership, and help shape the future of the clinical development organization. The ideal candidate combines deep oncology expertise with hands-on execution, thrives in an entrepreneurial environment, and enjoys building alongside a collaborative team.
Reports to: Chief Medical Officer
Location: Remote (U.S.)
Responsibilities:
Clinical Development Strategy & Medical Leadership
  • Lead the overall medical strategy for assigned oncology programs, ensuring scientific rigor, patient safety, and successful execution.
  • Develop and present cross-functional team recommendations to the leadership team.
  • Serve as the senior medical representative on cross-functional program teams, partnering closely with Clinical Operations, Regulatory Affairs, Biometrics, Translational Medicine, Pharmacovigilance, and Clinical Pharmacology.
  • Contribute to overall portfolio strategy and clinical development planning.
  • Represent the company with investigators, key opinion leaders, advisory boards, partners, and regulatory agencies.

Medical Monitoring & Patient Safety
  • Support medical monitoring across the studies providing consistency and oversight.
  • Provide ongoing medical oversight to ensure patient safety, protocol compliance, and high-quality clinical execution.
  • Review eligibility assessments, protocol deviations, safety events, and emerging efficacy data.
  • Partner with Pharmacovigilance to oversee SAE review, signal detection, benefit-risk assessments, and safety governance.

Clinical Data Review & Scientific Oversight
  • Lead ongoing review and interpretation of clinical data to ensure scientific integrity and data quality.
  • Identify emerging safety, efficacy, and operational trends to support informed development decisions.
  • Partner with Clinical Operations, Data Management, and Biostatistics to ensure robust data quality and timely database locks.
  • Guide interpretation of study results and support development of clinical study reports.

Regulatory & Scientific Leadership
  • Provide medical leadership for regulatory interactions, including briefing documents, health authority meetings, INDs, NDAs/BLAs, and other regulatory submissions.
  • Lead the medical review of protocols, informed consent documents, investigator brochures, and clinical study reports.
  • Drive scientific communications including abstracts, manuscripts, congress presentations, and external publications.
  • Support due diligence activities, business development opportunities, and strategic collaborations as appropriate.

Cross-Functional Leadership
  • Provide medical leadership across a highly collaborative, matrixed organization.
  • Mentor and influence cross-functional teams while fostering a culture of scientific excellence, accountability, and innovation.
  • Contribute to company-wide initiatives beyond assigned programs as a key member of the clinical leadership team.

Requirements:
  • M.D. degree with board certification and clinical experience as an attending physician.
  • 5-10 years of experience in the biotechnology and/or pharmaceutical industry, with progressive medical leadership responsibilities.
  • Experience within small biotechnology companies, with demonstrated success operating in lean, entrepreneurial environments.
  • Significant experience in oncology drug development.
  • Experience serving as Medical Monitor for interventional oncology clinical trials.
  • Demonstrated experience leading cross-functional clinical development teams.
  • Experience interpreting clinical data and guiding development decisions.
  • Strong understanding of regulatory requirements and experience supporting interactions with global health authorities.
  • Outstanding communication, executive presence, and stakeholder management skills.
  • Highly collaborative with a hands-on, solution-oriented approach.

Preferred Experience:
  • Clinical expertise in breast and/or endometrial oncology.
  • Prior experience as an attending physician in oncology.

Compensation Range: $320,000 - $425,000 (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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