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Clinical Development Jobs in Texas (NOW HIRING)

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 ...

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 ...

Ability to understand and navigate complex clinical development processes and cross-functional interdependencies * Strong analytical and problem-solving skills with the ability to assess operational ...

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 ...

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 ...

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 ...

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 ...

Train staff and support ongoing clinical development Qualifications * BCBA Certification required * Texas Licensure (or eligibility/apply upon hire) * Master's Degree in Behavior Analysis or related ...

New

Life Science Clinical Manager

Dallas, TX · On-site +1

$64K - $88K/yr

Supporting business development efforts through proposal development, client presentations, and practice-building activities A successful candidate would possess these skills: * Ability to work ...

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Showing results 1-20

Clinical Development information

See Texas salary details

$13

$32

$83

How much do clinical development jobs pay per hour?

As of Jul 19, 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.

How much does a clinical development trial lead make?

A clinical development trial lead at Eli Lilly typically earns between $120,000 and $160,000 annually, depending on experience and location. The role often requires strong project management skills and knowledge of clinical trial processes, with some positions offering additional bonuses or benefits.

What jobs pay $500,000 a year in the US?

In clinical development, senior roles such as Vice President or Chief Medical Officer can reach or exceed $500,000 annually, especially in large pharmaceutical or biotech companies. These positions typically require extensive experience, advanced degrees, and leadership skills, often involving strategic decision-making and regulatory oversight.

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.

What is the highest paying job in clinical research?

The highest paying roles in clinical research are often senior positions such as Clinical Development Director or Vice President of Clinical Development, which can offer salaries exceeding $150,000 annually. These roles typically require extensive experience, advanced degrees, and leadership skills, and they oversee large-scale clinical programs and strategic planning.

What are the key skills and qualifications needed to thrive in Clinical Development, and why are they important?

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 cities in Texas are hiring for Clinical Development jobs? Cities in Texas with the most Clinical Development job openings:
Senior Clinical Scientist

Senior Clinical Scientist

Faeth Therapeutics

Austin, TX • Remote

$150K - $200K/yr

Other

Medical, Dental, Vision, Life, Retirement

Re-posted 28 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.